Copper ion-comprehensive formulation to improve embryo implantation

Description

TECHNICAL FIELD

[0001] The present disclosure relates to a formulation for use in enhancing implantation of transferred embryos to a subject.PRIORITY DOCUMENT

[0002] The present application claims priority from Australian Provisional Patent Application No 2018901900 titled "Method for enhancing embryo implantation" filed on 29 May 2018.BACKGROUND

[0003] While huge improvements in IVF treatment over the last three decades have considerably advanced the understanding of how to optimise embryo development in vitro, very little advancement has been made regarding methods for optimising or enhancing the successful implantation of transferred embryos. Even today, the transfer of a good morphology, genetically normal embryo to the uterus of a "fertile" recipient (i.e. a woman with no impediments to her own fertility potential, such as pure male factor infertility) still does not guarantee successful implantation, with up to half of these "top quality" embryos failing to implant (Dahdouh et al., 2015). As such, human IVF can be considered to be very inefficient compared to species such as mice and rabbits where in excess of 95% of embryos successfully implant (Valbuena et al., 2017). Further, many women undertaking IVF treatment undergo the transfer of multiple good quality embryos and never have a successful pregnancy, suggesting a major impediment to implantation in this recurrent implantation failure (RIF) cohort. Moreover, many women are childless because their embryos fail to successfully implant, rather than being incapable of producing embryos (Martin, 1995), which of course implies an underlying implantation deficit.

[0004] To date, the only treatment known to augment implantation in RIF is disruption of the endometrium, either by curettage (also known as "endometrial scratching") (Nastri et al., 2015) or the insertion and subsequent removal of a contraceptive intra-uterine contraceptive device (IUCD) (Mao et al., 2017). It is not fully understood how this process enhances implantation, but it has been reported that the inflammatory reaction associated with endometrial disruption causes the release of cytokines and growth factors known to enhance embryo development (Liang et al., 2015). However, these current approaches to treat RIF have several disadvantages. First, they are generally conducted at least one menstrual cycle before the actual embryo transfer, allowing the damaged endometrium to be shed with menses and then time to repair itself - disruption of the endometrium (curettage) in the same menstrual cycle as an embryo transfer has been reported to impair implantation (Karimzade et al., 2010) as anticipated given that this process disrupts endometrial integrity and is associated with significant bleeding within the uterine cavity. Secondly, the process of taking an endometrial biopsy or insertion of an IUCD is painful to the recipient. As such, an ideal therapy would be one that is relatively painless, free of side effects and can be conducted in the same menstrual cycle as the anticipated embryo transfer.

[0005] It is presently unclear why human reproduction is less efficient than most other animal species. However, significant inter-species differences in early reproductive events may account for this anomaly, plus provide some insight into how implantation may be enhanced in humans. In prolific breeders such as rodents, rabbits and pigs, the cervix remains open around the time of mating, thereby allowing large volumes of seminal plasma and sperm to bathe the uterine endometrium and initiate the production of growth factors and cytokines, and additionally lead to the generation of a prominent post-mating uterine inflammatory response (Schjenken and Robertson, 2014; Robertson and Sharkey, 2016). This inflammatory reaction to semen remodels the uterine lining, as well as facilitates the growth and development of the embryo. Surgical removal of male accessory sex glands (prostate, seminal vesicle), thereby blocking uterine exposure to seminal plasma, results in a significantly diminished uterine inflammatory reaction and impaired implantation, underlying the reproductive importance of this response (Schjenken and Robertson, supra; Robertson and Sharkey, supra). However, the uterine cavity of women is exposed to a relatively low number of sperm and associated seminal plasma proteins because sperm must pass through the cervical mucous "filter" before reaching the uterus (Schjenken and Robertson, supra). This significantly different reproductive physiology between species means that women's exposure to semen following intercourse has less potential to trigger an inflammatory response capable of augmenting implantation compared to intra-uterine ejaculating animals.

[0006] Aside from seminal plasma, other triggers for uterine inflammation have been reported. For example, zinc and copper metal ions are known to be cytotoxic to endometrial cells in culture (Wu et al., 2012), and create an intra-uterine inflammatory response in the context of exposure to an IUCD (Sadovsky et al., 1975; Stanford and Mikolajczyk, 2002). While this IUCD-related endometrial inflammation is known to be contraceptive, impairing successful implantation of embryos (Kelly et al., 1969; Sheppard, 1987; Stanford and Mikolajczyk supra), the present inventor(s) postulated that a shorter period of exposure of the endometrium to copper ions and / or zinc ions, or at a lower dose, may produce a less intense inflammatory response that might possibly be capable of up-regulating the production of beneficial cytokines such as Vascular Endometrial Growth factor (VEGF) and Leukaemia inhibitory factor (LIF), but insufficient to cause harmful endometrial disruption that is normally observed in IUCD users.

[0007] The process of implantation of an embryo is a complex cascade of events requiring precise interaction between the action of ovarian steroids (e.g. estrogen and progesterone), and paracrine secretions from the embryo itself (e.g. hCG and cytokines) on the endometrium (Norwitz et al., 2001). Following ovulation and the subsequent rise in serum progesterone, endometrial glandular epithelial cells transform into highly active secretory cells that synthesise various substances (e.g. nutrients, growth factors and cytokines) that can enhance the development of the embryo and alter endometrial function. The uterine epithelium's production of LIF and VEGF are two key cytokines that play a critical role in aiding implantation (Norwitz et al., supra).Evidence supporting a critical role for LIF in implantation

[0008] There is a considerable amount of evidence that points to a critical role for LIF in embryo implantation such as: 1. In the LIF "knock-out" mouse (i.e. a mouse model with no LIF production), normal embryos are created, yet they fail to implant into the uterus (Stewart et al., 1992; Chen et al., 2002). However, transfer of these LIF - / - embryos to wild type (LIF-producing) mice, or the artificial delivery of exogenous LIF to LIF - / - mice by injection on day 4 of pregnancy, restores normal implantation capacity (Stewart et al., supra; Chen et al., supra). Further, tissue-specific ablation of the LIF receptor in the murine uterine epithelium also results in implantation failure (Cheng et al., 2017). All these findings suggest that LIF activity is absolutely critical for implantation in mice. 2. The production of LIF by the endometrium peaks in the luteal phase of fertile women, at the precise time that the embryo normally initiates implantation (Charnock-Jones et al., 1994; Cullinan et al., 1996). 3. Endometrial LIF production is reduced in women with recurrent IVF implantation failure (Mikolajczyk et al., 2007; Choi et al., 2016), suggesting a critical role for LIF in the implantation process. 4. The addition of LIF to murine embryos in culture has been reported to enhance endometrial development to the "hatched" blastocyst stage, as well as increase trophoblast outgrowth in vitro (Lavranos et al., 1995). Similarly, exposure of murine embryos to LIF in vitro and their subsequent transfer using a trans-cervical technique similar to human IVF, has been reported to enhance implantation and pregnancy rates (Mitchell et al., 2002). 5. Conversely, blocking LIF action in vitro using either LIF neutralising antibodies (Mitchell et al., supra) or a polyethylene glycosylated LIF antagonist (Lalitkumar et al., 2013) has been reported to inhibit implantation potential in mice and humans respectively. Moreover, the delivery of LIF neutralising antibody to the uterine cavity on day 5 of pregnancy has been shown to significantly impair implantation in rhesus monkeys (Sengupta et al., 2006). 6. Poor endometrial development (thin endometrium), possibly mediated by insufficient vascular perfusion of the endometrium (Jinno et al., 2001), is a known cause for implantation failure. There is significant evidence that LIF is involved in angiogenesis in the endometrium and placenta (Alfer et al., 2017).

[0009] In summary, endometrial LIF production increases after ovulation and appears to assist implantation by enhancing embryo development, while also initiating events in the endometrium that appear to be critical for initial attachment and invasion of the embryo (i.e. implantation). Further, low endometrial LIF production is associated with reduced IVF success and infertility of unknown aetiology. Moreover, exposure to copper in the form of a copper-containing IUCD has previously been reported to decrease endometrial LIF expression and impair implantation (Güney et al., 2007). However, the impact of shorter periods of copper (or zinc) exposure on endometrial LIF production was hitherto unknown.Evidence supporting a critical role for VEGF in implantation

[0010] There is also a considerable amount of evidence that points to a critical role for VEGF in embryo implantation, including: 1. The production of VEGF by the endometrium peaks in the mid-luteal phase of fertile women, at the precise time that the embryo normally initiates implantation. However, this mid-luteal peak in VEGF production is not seen in women with recurrent IVF implantation failure (Jee et al., 2009), suggesting a critical role for VEGF in the implantation process. 2. VEGF initiates endometrial tissue oedema by increasing vessel permeability and enhancing production of vasodilators (Rockwell et al., 2002). Oedema of the endometrial tissue (decidua) brings the uterine surface in close proximity to the blastocyst and appears to be important in establishing receptivity (apposition phase of implantation). 3. Gene polymorphisms that impair VEGF gene expression (e.g. the VEGF +405 CC polymorphism) have been found to be more common in women with recurrent IVF implantation failure (Boudjenah et al., 2012), while the VEGF +405 CC polymorphism is also associated with poorer implantation rates in "potentially fertile" women undergoing IVF for pure male factor infertility (Boudjenah et al., 2014). 4. Blocking VEGF activity by the administration of VEGF neutralising antibodies has been shown to prevent implantation in both primate and rodent models of pregnancy (Rockwell et al., supra; Ghosh and Sengupta, 2005). 5. The application of VEGF to embryos in culture has been shown to increase their speed of development / rate of cellular division (Hannan et al., 2011; Binder et al., 2014). 6. The in vitro exposure of human uterine epithelial cells to VEGF enhances their adhesiveness to common extracellular matrix (ECM) proteins found on the surface of the embryo (i.e. fibronectin and collagen), potentially assisting in the initial attachment of the embryo to the uterine epithelium (Binder et al., supra). 7. The glandular expression of VEGF in early luteal phase endometrial biopsies has been reported to be significantly higher in women who successfully conceived during IVF compared to those who did not conceive (Jinno et al., supra; Seo et al., 2011). 8. The level of VEGF in endometrial secretions obtained from uterine lavage (flushing uterine cavity with sterile saline in the mid-luteal phase) has been reported to be significantly lower in women experiencing recurrent IVF implantation failure than that seen in fertile controls (Hannan et al., supra), thereby suggesting VEGF may assist implantation. 9. The culture of mouse embryos in VEGF increased their adhesiveness to extracellular matrix (fibronectin)-coated plates in vitro, while also increasing the successful implantation of these VEGF-exposed embryos when transferred to pseudo-pregnant recipients (Binder et al., supra). 10. VEGF is known to play a critical role in the development of new capillaries (angiogenesis) and vascular perfusion of tissue, with thin endometrial development being linked to low capillary density and endometrial stromal VEGF expression (Miwa et al., 2009).

[0011] In summary, the available evidence suggests that endometrial-derived VEGF plays an important role in facilitating implantation by accelerating the development of the pre-implantation embryo, enhancing the adhesive interaction between the embryo and the uterine epithelium (improved binding to ECM proteins), while also increasing the underlying endometrial stroma oedema. A deficiency of VEGF action (e.g. through poor production by the epithelium or by the blocking of the action of VEGF) impedes implantation. As such, it has been considered that a therapy that could enhance endometrial production of VEGF may increase the rate of successful implantation of human embryos during IVF treatment. While copper has been previously reported to trigger an increase in endometrial VEGF production in IUCD users (Xin et al., 2004; Rafi et al., 2013), it was hitherto unknown whether a "short burst" exposure to copper ions, or the delivery of copper outside of the context of an IUCD "foreign body", would elicit a similar VEGF response, without causing endometrial disruption such as seen in IUCD users (Sadovsky et al., 1975; Stanford and Mikolajczyk, 2002). Similarly, prior to the experimentation described hereinafter, the impact of short term zinc exposure on endometrial VEGF production was unknown.

[0012] Mao et al. (Short-term copper intrauterine device placement improves the implantation and pregnancy rates in women with repeated implantation failure, Fertil Steril. 2017, 108; 55-61) mentions that short-term copper intrauterine device placement enhances pregnancy rates of women with repeated implantation failure.

[0013] The present disclosure relates to a formulation for use in enhancing implantation of transferred embryos to a subject. The formulation, involving the use of copper and optionally zinc ions, potentially offers a simple and relatively inexpensive treatment to enhance embryo implantation, particularly in women who have experienced recurrent implantation failure (RIF) following IVF or other assisted reproductive technology treatments.

[0014] The present invention is defined by the claims. Any subject-matter falling outside the scope of the claims is provided for information only. Methods of IVF and intrauterine insemination referred to in this description are not part of the present invention.SUMMARY

[0015] In a first aspect, the present disclosure provides a formulation comprising copper ions for use in a method of enhancing embryo implantation in a subject (i.e. a woman or other female animal), wherein the method comprises administering to the uterine cavity of the subject a formulation comprising copper ions in an amount effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF), wherein the copper ions are provided in a solution or gel form, wherein the formulation provides copper ions to the uterine fluid in an amount in the range of 0.025 µg to 12.5 µg per administration, (i) wherein the subject is hoping to achieve pregnancy through natural conception, and the formulation is administered to the subject prior to ovulation and within the same menstrual cycle, or (ii) wherein the subject is undergoing treatment by assisted reproductive technology involving the transfer of embryo, and the formulation is administered to the subject prior to embryo transfer and within the same menstrual cycle, or (iii) wherein the subject is undergoing treatment by intra-uterine insemination (IUI), and the formulation is administered to the subject prior to IUI and within the same menstrual cycle.

[0016] -

[0017] The formulation is particularly suitable for use with women undergoing treatment by any of the assisted reproductive technologies, and particularly those involving the transfer of embryos such as in vitro fertilisation (IVF) and variants including IVF-ICSI (intracytoplasmic sperm injection).

[0018] In an aspect, the present disclosure provides a formulation for enhancing embryo implantation in a subject, said formulation being suitable for administration to the uterine cavity and comprising copper in an amount effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF), and wherein said formulation optionally comprises one or more pharmaceutically acceptable carrier and / or excipient.

[0019] In some preferred embodiments, the copper is provided in a solution form, such as a solution comprising copper chloride (CuCl 2 ).BRIEF DESCRIPTION OF FIGURES

[0020] Figure 1 provides graphical results showing the effect of metal ions provided by CuCl 2 (A) and ZnCl 2 (B) solutions on the production of LIF from cultures of the human Ishikawa endometrial adenocarcinoma cell line (Ishikawa cells); Figure 2 provides graphical results showing the effect of metal ions provided by CuCl 2 (A) and ZnCl 2 (B) solutions on the production of VEGF from cultures of Ishikawa cells; Figure 3 shows the results of experimentation conducted to assess the amount of copper and zinc ions released from metal implants into cultures of Ishikawa cells in αMEM or G2 culture media. The metal implants, (A) copper sheet implant (Cu) and (B) copper-zinc sheet bimetal implant (CuZn), were placed into the cell cultures for durations of 2 minutes and 5 minutes; Figure 4 provides graphical results showing the effect of metal ions released from various metal implants (i.e. a copper sheet implant (Cu), a copper-zinc sheet bimetal implant (CuZn), a zinc sheet implant (Zn), a zinc-aluminium sheet bimetal implant (ZnAl), and zinc-gold sheet bimetal implant (ZnAu)), on (A) LIF production and (B) VEGF-A production from Ishikawa cells. Measurements were taken from the culture supernatants following 8 hour cultures. The cells were exposed to the metal implants for 2 mins; Figure 5 provides graphical results contrasting the stimulation of (A) LIF production and (B) VEGF production from Ishikawa cells cultured in "conditioned media" (i.e. including copper and zinc ions); the experiment for LIF production also included a positive control where Ishikawa cells were cultured in culture media with a 2 minute exposure to a copper-zinc sheet bimetal implant (CuZn); Figure 6 provides graphical results obtained following 8 hour cultures of Ishikawa cells with 2 and 5 min exposures to metal implants (namely, a copper sheet implant (Cu), a zinc sheet implant (Zn), and a copper-zinc sheet bimetal implant (CuZn)). The graphs show the effect of the metal implant exposures on LIF production (A, B) and VEGF production (C, D); Figure 7 provides examples of images showing embryo implantation outgrowth following culture of the day 3 murine embryos in: (A) fresh G2 media (control), (B) G2 media that had been conditioned by Ishikawa cell culture, and (C) G2 media that had been conditioned by Ishikawa cell culture with a two minute exposure to a copper-zinc bimetal implant; and Figure 8 shows the results of the extent of embryo implantation outgrowth (embryo attachment surface area, mm 2< ) following culture of the day 3 murine embryos in: fresh G2 media (control), G2 media that had been conditioned by Ishikawa cell culture, and G2 media that had been conditioned by Ishikawa cell culture with a two minute exposure to a copper-zinc bimetal implant. The results were assessed at 66 hour (A) and 90 hour (B) time points. DETAILED DESCRIPTION

[0021] In experimentation described hereinafter, the present inventor(s) found that human endometrial cells subjected to a short term exposure of copper ions (Cu 2+< ), as provided by salt solutions, produced increased amounts of leukaemia inhibitory factor (LIF) and vascular endothelial growth factor (VEGF), both of which are believed to have an important role in embryo implantation. Moreover, when day 3 embryos were grown in "conditioned" media including the metal ions, significant increases in the surface area of trophoblast outgrowth resulted, thereby indicating improved embryo health and implantation potential. The present disclosure is therefore directed to a novel formulation, involving the use of copper and optionally zinc ions to enhance endometrial production of LIF and / or VEGF, to enhance embryo implantation in women (and other female animals) including women who have experienced recurrent implantation failure (RIF) following IVF or other assisted reproductive technology treatments.

[0022] In a first aspect, the present disclosure provides a formulation comprising copper ions for use in enhancing embryo implantation in a subject (i.e. a woman or other female animal), wherein the method comprises administering to the uterine cavity of the subject a formulation comprising copper ions in an amount effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF), wherein the copper ions are provided in a solution or gel form, wherein the formulation provides copper ions to the uterine fluid in an amount in the range of 0.025 µg to 12.5 µg per administration, (i) wherein the subject is hoping to achieve pregnancy through natural conception, and the formulation is administered to the subject prior to ovulation and within the same menstrual cycle, or (ii) wherein the subject is undergoing treatment by assisted reproductive technology involving the transfer of embryo, and the formulation is administered to the subject prior to embryo transfer and within the same menstrual cycle, or (iii) wherein the subject is undergoing treatment by intra-uterine insemination (IUI), and the formulation is administered to the subject prior to IUI and within the same menstrual cycle.

[0023] The formulation is suitable for use with women undergoing treatment by any of the assisted reproductive technologies, such as those involving the transfer of embryos such as in vitro fertilisation (IVF) and variants including IVF-ICSI (intracytoplasmic sperm injection) and in vitro maturation (IVM) treatments, as well as intrauterine-insemination (IUI) therapy. However, the use of the formulation is also applicable for women wanting to improve their prospects of pregnancy through natural conception.

[0024] The formulation may be particularly suitable for use with women who show inadequate or "thin" endometrial development (e.g. an endometrial thickness of 7 mm or less), which is a recognised cause of infertility and implantation failure following embryo transfer (Kasius et al., 2014; Yuan et al., 2016). In this regard, it is considered that by stimulating endometrial production of LIF and / or VEGF, which are both believed to stimulate endometrial angiogenesis, the method may be performed so as to improve angiogenesis and thereby treat thin endometrium-related implantation failure. Accordingly, the present disclosure also extends to a method of treating women experiencing inadequate endometrial development. Women experiencing inadequate endometrial development may be readily identified by standard ultrasound imaging (e.g. transvaginal ultrasound).

[0025] Further, while the emphasis of the present disclosure resides with women, those skilled in the art will recognise that the formulation disclosed herein are also applicable to other non-human female subjects (i.e. other female animals) such as, for example, livestock (e.g. cattle, horses and sheep), exotic animals (e.g. pandas, big cats such as tigers and lions, elephants and the like) and companion animals (such as dogs and cats), particularly where assisted reproductive technologies (especially those involving the transfer of embryos) are being employed to assist in achieving pregnancy.

[0026] In some embodiments, the formulation of the first aspect comprises copper and, optionally, zinc.

[0027] In other embodiments, the formulation comprises copper or copper and zinc.

[0028] -

[0029] The copper may be present in the formulation in, for example, one or more of an elemental (e.g. pure), alloy, complexed, oxidised, salt (including esterified salts and other salts formed from organic acids) or solution forms. The copper is present in such a form that provides a source of copper ions within the uterus. Such a form may include nanoparticle forms. The formulation is in the form of a liquid or semi-solid form.

[0030] In some embodiments, the copper is provided in a solution form, such as a solution comprising copper chloride (CuCl 2 ), a solution comprising copper sulphate (CuSO 4 ), copper gluconate, a solution of copper chlorate (Cu(ClO 4 ) 2 ), a solution comprising copper nitrate (Cu(NO 3 ) 2 ) or a solution comprising copper bromide (CuBr) or mixtures thereof (e.g. a solution of CuCl 2 and copper gluconate). Such solutions may provide a source of copper ions within the uterus.

[0031] In other embodiments, the copper is provided in a semi-solid (e.g. gel or foam) form. For example, a gel comprising CuCl 2 or a gel comprising nanoparticles of copper or which comprise CuCl 2 . The gel may, for example, provide a short term depot dosage form within the uterus. As will be appreciated by those skilled in the art, biodegradable gel depots may also be formed in situ using well known injectable in situ depot-forming drug delivery systems. Such a gel may provide a source of copper ions within the uterus, which may enable a controlled and / or sustained release of copper ions. In some particular embodiments of suitable gel formulations, the copper may be formulated with hydroxyethyl cellulose and glycerol, and in one example, the copper may be formulated with ExEmgel ®< (IQ Medical Ventures BV; Rotterdam, The Netherlands).

[0032] -

[0033] It is to be appreciated that the formulation is something other than an IUCD.

[0034] Also, it is to be appreciated that the formulation used in the first aspect is not provided as any solid form or within any device that requires surgical removal from the uterus after treatment. In this regard, the dosage forms of the embodiments described above will, in many if not all cases, enable a relatively non-invasive and "comfortable" treatment by allowing administration by simple means (e.g. by the use of a device such as, for example, a flexible catheter "loaded" with the formulation and passed through the cervical canal and into the uterine cavity) without any need for subsequent removal of the formulation.

[0035] The formulation may comprise one or more pharmaceutically acceptable carrier and / or excipient, which may vary depending upon the dosage form to be adopted. For example, for a solution of a salt of copper , the formulation may comprise water or normal (isotonic) saline. For a gel comprising a salt of copper , the formulation may comprise a biocompatible and biodegradable polymer excipient (e.g. lactide / glycolide polymers, and hydroxyethyl cellulose etc); in such gels, the copper may be present as esterified salt(s), particularly one comprising a saturated fatty acid such as decanoic (capric) acid (e.g. copper (2 +< ) decanoate), or salt(s) of other organic acids such as salts of D-gluconic acid (e.g. copper gluconate). As would be appreciated by those skilled in the art, the formulation may further comprise one or more substance selected from preservatives (e.g. sodium benzoate, sorbic acid and esters of p-hydroxybenzoic acid), binders (e.g. starch, gelatin, natural sugars such as glucose and anhydrous lactose, and natural and synthetic gums such as acacia, hydroxyethyl cellulose, carboxymethyl cellulose and polyethylene glycol), lubricants (e.g. sodium oleate, sodium stearate, magnesium stearate and the like), humectants (e.g. glycerol), anti-oxidants, suspending agents, stabilising agents, coating agents and solubilising agents, as may be required and / or desirable for a particular dosage form.

[0036] Further, the formulation may comprise one or more other substance which stimulate the production or activity of LIF, VEGF or other cytokines, growth factors etc that may be beneficial to embryo implantation (e.g. integrins). For example, the formulation may further comprise an effective amount of benzoic acid which is believed to cause an increase in the expression of LIF and the integrins, V3 and V5, to promote embryo implantation (Korean Patent Publication No 20160108690).

[0037] The formulation is administered to the subject in an amount in the range of 0.025 µg to 12.5 µg copper ions, effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF).

[0038] In some embodiments, that amount will typically be one that provides copper ions to the uterine fluid in an amount that is at least 500 ppb. However, preferably, the formulation is administered to the subject in an amount that provides copper ions to the uterine fluid in an amount that is at least 1250 ppb (more, preferably, at least 2500 ppb. As will be readily appreciated by those skilled in the art, a sample of uterine fluid may be obtained by aspiration using an embryo transfer catheter (Ametzazurra et al., 2009) and assessed for metal ion content using mass spectroscopy. However, suitable amounts of the formulation (i.e. to provide copper ions to the uterine fluid in an amount that is at least 500) may otherwise be tested for by adding varying amounts of the formulation to a "model" uterine fluid and amount (e.g. a volume of 5 ml of a suitable culture medium such as αMEM or G2 media or a suitable embryo transfer medium) at 37°C and assessing the metal ion content by mass spectroscopy in a sample of the media taken at a suitable time point(s) (e.g. 2 minutes and / or 5 minutes after addition of the formulation). It is considered that the "release" of copper ions into the media will be substantially comparable to that which will occur in the uterus. Accordingly, detection of an amount of copper ions in the tested sample of at least 500 ppb may indicate an amount of the formulation (comprising copper) suitable for administration.

[0039] The amount of the formulation that is effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF) is an amount that provides copper to the endometrial fluid in an amount in the range of 0.025 µg to 12.5 µg (preferably about 0.25 µg to about 10 µg, more preferably about 0.5 µg to about 5 µg, and most preferably about 0.05 µg to about 2.5 µg).

[0040] In some embodiments of a formulation comprising a solution of CuCl 2 , the formulation comprises a concentration of CuCl 2 of at least about 20µM, preferably at least about 50 µM. In particular, the formulation preferably comprises a solution of CuCl 2 at a concentration in the range of about 20µM to about 200 µM, more preferably in the range of 50 µM to 150µM. Such a formulation may be administered to the subject in a volume of about 100 to 1000 µl, more preferably about 150 to 500 µl.

[0041] -

[0042] Where the subject is undergoing treatment by any of the assisted reproductive technologies involving the transfer of embryos, the formulation is administered to the subject prior to embryo transfer and within the same menstrual cycle (which in the context of IVF, would be considered as the same IVF cycle). Preferably, the formulation is administered to the subject at a time prior to embryo transfer that is sufficient to stimulate a level of endometrial production of LIF and / or VEGF to enhance embryo implantation. Preferably, the subject is given a single administration of the formulation prior to embryo transfer. In some embodiments, the formulation is administered to the subject no more than 14 days prior to the embryo transfer, preferably, no more than about 10 days prior to the embryo transfer and, more preferably, no more than about 5 days prior to the embryo transfer. In some embodiments, the formulation is administered 5 days prior to the embryo transfer, or 4 days prior to the embryo transfer, or 3 days prior to the embryo transfer, or 2 days prior to the embryo transfer, or 1 day prior to the embryo transfer. In other embodiments, the formulation is administered on the same day as the embryo transfer; for example, shortly before the embryo transfer (e.g. within 3 hours, or 60 minutes, or 30 minutes, or 10 minutes, or 5 minutes, or 1 minute of the embryo transfer) or, less preferably, immediately after the embryo transfer (e.g. within 10 minutes of the embryo transfer). It may also be an option to administer the formulation concurrently with the embryo transfer. For instance, the embryo may be transferred to the subject in the formulation which might, in such embodiments, further comprise components and substances typically included in standard embryo transfer media (e.g. as found in EmbryoGlue ™< embryo transfer media; Vitrolife, Gothenburg, Sweden). Alternatively, the formulation may be provided for concurrent administration with the embryo transfer by coating or impregnating the embryo transfer catheter (or at least a portion of a distal section of an embryo transfer catheter that is inserted into the uterine cavity, or a part thereof) in the formulation; in such an embodiment, it may be preferred if a part of the distal section of the catheter that is a short distance away (eg 1-3 cm) from the tip of the catheter (from where the embryo is ejected) is coated or impregnated in the formulation.

[0043] Notwithstanding what is described in the preceding paragraph, in some preferred embodiments of the formulation for use according to the first aspect, there is no administration of formulation either at the time of embryo transfer (ie concurrently) or after the embryo transfer. That is, the use of such embodiments comprises administering the formulation only prior to embryo transfer, preferably as a single administration.

[0044] For women experiencing inadequate endometrial development, the formulation will be administered to the uterine cavity at least once in the relevant menstrual cycle, and preferably during the time between the cessation of the menses and ovulation or commencement of the increase in progesterone that accompanies ovulation. In some embodiments, the formulation may be administered on multiple occasions during this period (eg one administration per day over a series of days).

[0045] Where the subject is undergoing treatment by IUI, the formulation is administered to the subject prior to IUI and within the same menstrual cycle (i.e. within the same menstrual cycle as the insemination is being performed). Preferably, the formulation is administered to the subject at a time prior to ovulation / insemination that is sufficient to stimulate a level of endometrial production of LIF and / or VEGF to enhance embryo implantation. Preferably, the subject is given a single administration of the formulation prior to insemination. In some embodiments, the formulation is administered to the subject no more than 9 days prior to ovulation and, preferably, no more than about 5 days prior to ovulation. In some embodiments, the formulation is administered 5 days prior to ovulation, or 4 days prior to the ovulation, or 3 days prior to ovulation, or 2 days prior to ovulation, or 1 day prior to ovulation. In other embodiments, the formulation is administered on the same day as ovulation. Preferably, there is no administration of formulation either at the time of insemination (ie concurrently) or after the insemination. However, for women experiencing inadequate endometrial development, the formulation will be administered to the uterine cavity at least once in the relevant menstrual cycle; preferably during the time between the cessation of the menses and ovulation or commencement of the increase in progesterone that accompanies ovulation (e.g. the formulation may be administered on multiple occasions during this period (e.g. one administration per day over a series of days)).

[0046] Where the subject is hoping to achieve pregnancy through natural conception, the formulation is administered to the subject prior to ovulation and within the same menstrual cycle. Preferably, the formulation is administered to the subject at a time prior to ovulation that is sufficient to stimulate a level of endometrial production of LIF and / or VEGF to enhance embryo implantation. In some embodiments, the formulation is administered to the subject no more than 9 days prior to ovulation and, preferably, no more than about 5 days prior to ovulation. In some embodiments, the formulation is administered 5 days prior to ovulation, or 4 days prior to ovulation, or 3 days prior to ovulation, or 2 days prior to ovulation, or 1 day prior to ovulation. In other embodiments, the formulation is administered on the same day as ovulation. For women experiencing inadequate endometrial development, the formulation will be administered to the uterine cavity at least once in the relevant menstrual cycle; preferably during the time between the cessation of the menses and ovulation or commencement of the increase in progesterone that accompanies ovulation (e.g. the formulation may be administered on multiple occasions during this period (e.g. one administration per day over a series of days)).

[0047] The present disclosure provides a formulation for use in enhancing embryo implantation in a subject (i.e. a woman or other female animal), comprising inserting into the uterine cavity of the subject a device comprising the formulation comprising copper for a period of time that is effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF).

[0048] -

[0049] -

[0050] -

[0051] In an aspect, the present disclosure provides a formulation for enhancing embryo implantation in a subject, said formulation being suitable for administration to the uterine cavity and comprising copper in an amount effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF), and wherein said formulation optionally comprises one or more pharmaceutically acceptable carrier and / or excipient.

[0052] The formulation comprises copper and, optionally, zinc. In other embodiments, the formulation comprises copper or copper and zinc.

[0053] The copper may be present in the formulation in, for example, one or more of an elemental (e.g. pure), alloy, complexed, oxidised, salt (including esterified salts and other salts formed from organic acids) or solution forms. Preferably, the copper is present in such a form that may provide a source of copper ions within the uterus. The formulation may be in the form of, for example, a liquid or semi-solid form.

[0054] In some preferred embodiments, the copper is provided in a solution form, such as a solution comprising copper chloride (CuCl 2 ). Such a solution may provide a source of copper ions within the uterus. Preferably, the solution is an isotonic saline solution of CuCl 2 .

[0055] In other embodiments, the copper is provided in a semi-solid (e.g. gel or foam) form. For example, a gel comprising CuCl 2 or a gel comprising nanoparticles of copper or which comprise CuCl 2 . The gel may, for example, provide a short term depot dosage form within the uterus providing a source of copper ions within the uterus, which may enable a controlled and / or sustained release of copper ions (e.g. a gel wherein the copper is formulated with hydroxyethyl cellulose and glycerol).

[0056] In yet other embodiments, the copper is provided in a solid dosage form such as small, dissolvable crystals or other particles (e.g. a powder or metal nanoparticles) of, for example, crystals or other particles of CuCl 2 , which may be administered in a suitable carrier liquid or gel (e.g. which may be prepared shortly before administration) or as provided in a dissolvable tablet or capsule. Such crystals or other particles may provide a source of copper ions within the uterus.

[0057] The formulation may comprise one or more pharmaceutically acceptable carrier and / or excipient such as those described above. Also, the formulation may further comprise one or more substance selected from preservatives, binders, lubricants, anti-oxidants, suspending agents, stabilising agents, coating agents and solubilising agents, such as those described above. In addition, the formulation may comprise one or more other substances which stimulate the production or activity of LIF, VEGF or other cytokines, growth factors etc that may be beneficial to embryo implantation (e.g. integrins). The formulation may also comprise components and substances typically included in standard embryo transfer media.

[0058] In some preferred embodiments, the formulation comprises a solution of CuCl 2 comprising a concentration of CuCl 2 of at least about 20 µM, preferably at least about 50 µM. In particular, the formulation preferably comprises a solution of CuCl 2 at a concentration in the range of about 20 µM to about 200 µM, more preferably in the range of 50 µM to 150 µM.

[0059] Where the formulation is provided as a liquid (e.g. a formulation comprising a solution of CuCl 2 ), the formulation may be provided in a package or device adapted for administration of the formulation to the uterine cavity; for example, a flexible catheter "loaded" with the formulation which is adapted to be passed through the cervical canal and into the uterine cavity. Such a catheter may be akin to those used for the transfer of embryos (suspended in small volumes of transfer media) to women undergoing IVF treatment. The catheter may comprise a biocompatible polymer and be hermetically sealed for transport and storage containing the liquid formulation, which may be provided in a reservoir or bulb located at or adjacent to the tip of the catheter. The tip of the catheter may comprise a frangible section which may be broken just prior to use. Otherwise, the tip may be sealed with a readily removable cap or lid. The amount of the formulation contained within the catheter may be as little as 100 to 1000 µl or, more preferably, a volume in the range of about 150 to 500 µl.

[0060] -

[0061] -

[0062] The subject may be a woman undergoing treatment by any of the assisted reproductive technologies, particularly those involving the transfer of embryos such as in vitro fertilisation (IVF) and variants including IVF-ICSI (intracytoplasmic sperm injection) and in vitro maturation (IVM) treatments. However, the subject may also be a woman receiving intrauterine-insemination (IUI) therapy, or a woman wanting to improve their prospects of pregnancy through natural conception. The subject may also be selected from other non-human female subjects such as, for example, livestock.

[0063] The formulation is in the form of a liquid or semi-solid form. In some embodiments, the copper is provided in a solution form, such as a solution comprising copper chloride (CuCl 2 ). Such a solution may provide a source of copper ions within the uterus.

[0064] The formulation may comprise one or more pharmaceutically acceptable carrier and / or excipient such as those described above. Also, the formulation may further comprise one or more substance selected from preservatives, binders, lubricants, anti-oxidants, suspending agents, stabilising agents, coating agents and solubilising agents, such as those described above. In addition, the formulation may comprise one or more other substance which stimulate the production or activity of LIF, VEGF or other cytokines, growth factors etc that may be beneficial to embryo implantation (e.g. integrins).

[0065] In some preferred embodiments, the formulation comprises a solution of CuCl 2 comprising a concentration of CuCl 2 of at least about 20 µM, preferably at least about 50 µM. In particular, the formulation preferably comprises a solution of CuCl 2 at a concentration in the range of about 20 µM to about 200 µM, more preferably in the range of 50 µM to 150 µM. In some other preferred embodiments, the formulation comprises a solution of ZnCl 2 comprising a concentration of ZnCl 2 of at least about 20 µM, preferably at least about 50 µM. In particular, the formulation preferably comprises a solution of ZnCl 2 at a concentration in the range of about 20 µM to about 150 µM, more preferably in the range of 50 µM to 125 µM.

[0066] The method and formulation of the present disclosure is hereinafter further described by way of the following, non-limiting examples and accompanying figures.EXAMPLES Example 1 Effect of metal ions on in vitro LIF and VEGF production Materials and Methods

[0067] The human Ishikawa endometrial adenocarcinoma cell line (Sigma-Aldrich; St Louis, MO, United States of America) was used to model the endometrium's response to copper and zinc metal ions (Cu 2+< and Zn 2+< ). Cells were grown in T75 flasks (Nalge Nunc International, Rochester, NY, United States of America) in Ishikawa medium, consisting of αMEM (Sigma-Aldrich) supplemented with 5% foetal bovine serum (Invitrogen Corp, Carlsbad, CA, United States of America), 2 mM glutamine (Sigma-Aldrich) and 1% non-essential amino acids (Sigma-Aldrich) without antibiotics at 37°C under a gas atmosphere of 5% CO 2 in air. Medium was refreshed every 48 hours. Cells were subcultured using 0.25% trypsin / EDTA (Invitrogen). For metal ion exposure experiments, cells were seeded onto 2-well chamber slides (Ibidi, Martinsried, Germany). After the endometrial cells had attached and reached 80-90% confluence they were then exposed to copper and zinc metal ions using two approaches (salt solution or metal implant) as described below.Metal ions in solution

[0068] Copper or zinc chloride (Sigma-Aldrich) was dissolved in Ishikawa medium to produce salt solutions at various concentrations in the range of 0.2 µM and 200 µM, before being applied to Ishikawa cells seeded into 2-well chamber slides for a period of 8 hours. Following the 8 hours exposure, culture media were removed, centrifuged at 1000g for 10 minutes at 4°C to pellet any cellular debris, and then the supernatants were stored in Eppendorf tubes at -80°C. Subsequently, the supernatants were assayed for both LIF and VEGF content using a multiplex immunoassay system (elisakit.com, Scoresby, VIC, Australia).Metal implants

[0069] Implants composed of various metals were generated using either metal wire (copper) or metal sheets of various types (copper, zinc, aluminium and gold). In some cases, the implants comprised sheets of two metals (bimetal implants), particularly copper and zinc (CuZn), zinc and aluminium (ZnAl) and zinc and gold (ZnAu). Following heat sterilisation, the implants were placed in direct contact with Ishikawa cells and then seeded onto 2-well chamber slides in Ishikawa medium or G2 embryo culture medium (Vitrolife) using sterilised surgical tweezers for a period of between 1 and 5 minutes, before being removed. The Ishikawa cell supernatants were collected 4-8 hours later, centrifuged at 1000g at 4°C for 10 minutes, and then frozen at -80°C for later metal ion and cytokine assessment by mass spectroscopy.Results

[0070] With the solutions of metal ions, it was found that copper ions produced a significant increase in LIF production above baseline at a CuCl 2 concentration exceeding 2 µM (see Figure 1A), with LIF production increasing 420% above baseline at a concentration of 200 µM. No toxicity in relation to LIF production was observed in the tested dose range within the 8 hour incubation time frame. The zinc ions also produced a significant increase in LIF production compared to controls at ZnCl 2 concentrations ranging from 50 µM to 150 µM (see Figure 1B). However, when administered at doses exceeding 150 µM, the zinc ions appeared to cause toxicity, with a reduction in LIF production being observed (Figure 2A). In relation to VEGF production, the copper chloride solutions produced a significant increase in VEGF production at concentrations above 20 µM, peaking at 100 µM CuCl 2 concentration. On the other hand, zinc chloride produced no significant increase in VEGF compared to controls, but did appear to reduce VEGF production from a concentration of 150 µM (Figure 2B).

[0071] With the copper wire / copper sheet and CuZn bimetal sheet implants, mass spectroscopy confirmed the release of copper and zinc ions into conditioned αMEM / G2 medium over relatively short periods of time (see Figures 3A and 3B; nb. in the results obtained with the copper implant and shown in Figure 3A, a small amount of zinc was detected due to the presence of zinc in the αMEM media). As expected, the presence of zinc (in the CuZn bimetal implant) slowed the release of copper ions into the solution (Figure 3B), with zinc appearing to act as a sacrificial anode. In addition, it was observed that, like the CuCl 2 and ZnCl 2 solutions, the copper ions and zinc ions from the wire and sheet metal implants increased endometrial cell culture production of LIF and VEGF in multiple replicates (Figures 4A and 4B). The response was considerably better for copper or copper-zinc implants than for any of the other metal combinations.

[0072] Further experiments were conducted to determine whether this increase (i.e. up-regulation) of LIF and VEGF production was related to the release of metal ions, the associated creation of a galvanic current during in situ corrosion or the physical presence of the metal implant ("foreign body" reaction). These experiments involved adding 1.5 ml of Ishikawa αMEM medium to each well of 2-well chamber slides without cells and thereafter adding CuZn bimetal implants for a period of 2 minutes (after which time they were removed using sterile tweezers). The resultant "conditioned media" was then added to 2-well slides containing Ishikawa cells and incubated for a period of 8 hours, thereby exposing these cells to metal ions but not the physical presence of the implant or any galvanic electrical current created by corrosion of the implant. These experiments revealed that conditioned media containing copper ions and zinc ions was still capable of eliciting an increase in LIF and VEGF production above that seen in control unexposed cultures (see Figures 5A and 5B).Example 2 Effect of metal ions on embryo development and attachment Materials and Methods

[0073] Ishikawa cells were seeded onto 2-well chamber slides in Ishikawa medium until they reached 80-90% confluence. Then, 5 minutes prior to exposure to metal implants, the medium was changed to G2 embryo culture medium, and the Ishikawa cells exposed to copper, zinc or copper-zinc bimetal implants for either 2 or 5 minutes duration (or remained unexposed (control)), and the resulting G2 culture media collected 8 hours later. The supernatants were then analysed as described above in Example 1 to confirm that the metal implant exposure resulted in an up-regulation in endometrial LIF and VEGF production (see Figures 6A-D).

[0074] To determine whether metal ions were capable of enhancing embryo implantation, post-compaction mouse embryos were exposed to the "conditioned media" prior to undergoing outgrowth assays. In particular, pronucleate oocytes were collected from superovulated female F1 mice ~21-22 hours post-hCG. Following cumulus cell removal, oocytes were cultured in 20 µl drops (10 embryos / drop) of G1 medium under paraffin oil (Vitrolife) at 37°C in 6% CO 2 , 5% O 2 and 89% N 2 . After 48 hours, compacting and morulae stage embryos were randomly transferred to culture in either (i) control G2 medium (Vitrolife) that had not been exposed to Ishikawa cells; (ii) individual culture in 2 µl of control, Ishikawa exposed G2; or (iii) individual culture in 2 µl drops of 2 minute copper-zinc bimetal implant exposed G2 medium. After 48 hours, the capacity of blastocysts to undergo outgrowth was assessed in the following manner. First, flat bottomed 96-well tissue culture plates (BD Biosciences, Franklin Lakes, NJ, United States of America) were coated with fibronectin (10 µg / ml; BD Biosciences), rinsed twice with sterile PBS and incubated with 4 mg / ml bovine serum albumin (Sigma-Aldrich). Wells were then rinsed before being filled with G2 medium supplemented with 5% FCS and equilibrated at 37°C under paraffin oil (Ovoil; Vitrolife) for 3 hours prior to the addition of blastocysts. Hatched and hatching blastocysts from each respective treatment were placed into prepared wells (1 embryo per well) and incubated for 90 hours. During the culture period, outgrowths were examined and images taken at 66 and 90 hours post-transfer to the outgrowth plate with an inverted microscope (Nikon Eclipse TS100-F) equipped with a heated stage set at 37°C. The extent of outgrowth for each treatment was obtained by measuring the area of outgrowth in each of the images taken across the experiment using ImageJ. All images were collected and analysed at matching magnification.Results and Discussion

[0075] While no difference in the rate of embryo development was observed when the conditioned medium from the copper and zinc ion-exposed cultures was added to murine day 3 embryos, there was a very significant increase in the surface area of trophoblast outgrowth to the fibronectin-coated plates 3-4 days later (see Figures 7, 8A and 8B), thereby signifying improved embryo health and implantation potential.

[0076] This latter observation is important for two reasons. First, it confirms the ability of copper ions and zinc ions to mediate up-regulation of endometrial LIF / VEGF production to enhance implantation processes. Secondly, it confirms that while copper ions and zinc ions have traditionally been perceived as toxic to pre-implantation embryo development (Brinster and Cross, 1972; Webb et al., 1973; Holland and Pike 1978; Erbach et al., 1995), this toxicity was not significant with the short term exposure in these experiments. Therefore, despite nearly half a century of teaching suggesting that copper or zinc containing IUCDs provide effective contraception (Stanford, 2002), it is clear from the results described herein that short term delivery of copper ions and / or zinc ions to the endometrium can actually enhance the implantation processes.

[0077] While not wishing to be bound by theory, it is considered that the discrepancy observed between the experimentation described herein showing a beneficial effect of copper on endometrial function (in terms of LIF / VEGF production) and the well described detrimental effect of copper on endometrial health and function in IUCD users, may be explained by the considerable difference in the "dose" of copper delivered to the endometrium. That is, multiple studies have examined the rate of copper delivery in IUCD users, with this rate varying depending on the surface area of copper in the IUCD device and the time since initial insertion. In one such study, the average amount of copper delivered to the uterus was reported to vary from between 13.3 µg and 116.7 µg per day (Timonen, 1976). Other studies have reported mean rates of delivery as 26.7 µg (Chantler et al., 1984), 14 µg (Larsson et al., 1981) and 45 µg of copper per day (Hagenfeldt, 1972). In the experimentation of Example 1, a 4-fold increase in endometrial LIF production was observed at a CuCl 2 concentration of 200 µM. If it is assumed that the uterine cavity of a woman has a volume of approximately 150 µl (Casslen, 1986), the corresponding amount of copper that would need to be applied in vivo to give a dose equivalent to 200 µM would be 1.91 µg of copper. Further, as a relative decline in endometrial VEGF production was observed at a CuCl 2 concentration exceeding 100 µM in vitro (Figure 2A), it is possible that the optimal quantum of copper needed to elicit a positive endometrial response in vivo is closer to 1 µg, a level approximating only 1 -7% of the amount of copper IUCD users are exposed to daily (Hagenfeldt, supra; Timonen, supra; Larsson et al., supra; Chantler et al., supra). As such, it is considered that the dose of copper required to elicit a beneficial endometrial response (i.e. an increase in LIF / VEGF) that can enhance embryo implantation must be below 13.3 µg, the lowest reported rate of copper released per day by an IUCD device capable of impairing implantation (Copper T 100 mm 2< IUCD; Timonen, supra). In the experimentation of Example 1, 20 µM of CuCl 2 was the lowest amount of copper confirmed to elicit an increase in endometrial LIF and VEGF, which equates to an in vivo uterine delivery dose of 0.191 µg of copper. Thus, in some preferred embodiments of the methods of the present disclosure, the formulation / device would be administered / inserted to the subject so as to deliver a dose of copper between 0.1 µg and 10 µg to the uterine cavity. A similar dose range may also be preferred for zinc.

[0078] In addition to the up-regulation of endometrial LIF / VEGF production, copper ions and zinc ions may also enhance implantation processes by destroying harmful bacteria that may be present in the uterus. That is, while classically the uterus has been considered a sterile region devoid of potentially pathogenic bacteria, it is now recognised that colonisation of the endometrium with certain bacteria is seen in some infertile women and is associated with impaired implantation potential (Moreno et al., 2016). As both copper and zinc are known to possess anti-bacterial qualities (Vincent et al., 2016; Siddiqi et al., 2018), it is possible that the local application of copper ions or zinc ions (or in combination) to the uterine cavity may kill or inhibit these potentially implantation-impairing bacteria in this group of patients, thereby enhancing their natural and IVF assisted fertility potential.Example 3 Prophetic example of treatment to enhance implantation of transferred embryo

[0079] An isotonic saline solution was prepared comprising CuCl 2 at a concentration of 150 µM and ZnCl 2 at 100 µM.

[0080] A 35 year-old woman who had experienced recurrent implantation failure (RIF), in particular five failed IVF cycles with good quality embryos, presented to the clinic 5 days ahead of an anticipated further transfer of an IVF embryo. Using a transfer catheter typically used for intra-uterine insemination therapy (e.g. Soft-Pass ™< insemination catheter; Cook Medical Inc., Bloomington, IN, USA) loaded with a 200 µl amount of the CuCl 2 / ZnCl 2 solution, the solution was administered to the uterine cavity.

[0081] On the scheduled day for embryo transfer, the woman re-presented to the clinic and received a good quality embryo in accordance with usual protocols.

[0082] Throughout the specification and the claims that follow, unless the context requires otherwise, the words "comprise" and "include" and variations such as "comprising" and "including" will be understood to imply the inclusion of a stated integer or group of integers, but not the exclusion of any other integer or group of integers.REFERENCES

[0083] Alfer J et al., Geburtshilfe Frauenheilkd 77(7):756-764 (2017). Ametzazurra A et al., Hum Reprod 24(4):954-965 (2009). Binder NK et al., Hum Reprod 29(10):2278-2286 (2014). Boudjenah R et al., J Assist Reprod Genet 29(12):1415-1420 (2012). Boudjenah R et al., PLoS One 9(9):e108287 (2014). Brinster RL, Cross PC., Nature 238(5364):398-399 (1972). Casslén B. J Reprod Med 31(6):506-510 (1986). Chantler EN et al., Br J Obstet Gynaecol 91(2):172-181 (1984). Charnock-Jones DS et al., J Reprod Fertil 101(2):421-426 (1994). Chen JR et al., Endocrinology 141(12):4365-4372 (2000). Cheng J et al., Endocrinology 158(6):1916-1928. doi: 10.1210 / en.2017-00103 (2017). Choi et al., PLoS One 11(6):e0157696. doi: 10.1371 / journal .pone.0157696 (2016). Cullinan EB et al., Proc Natl Acad Sci U S A 93(7):3115-3120 (1996). Dahdouh EM et al., Reprod Biomed Online 30(3):281-289 (2015). Erbach GT et al., Hum Reprod 10(12):3248-3254 (1995). Ghosh D, Sengupta J. Contraception 71(4):294-301 (2005). Güney M et al., Eur J Contracept Reprod Health Care 12(3):212-219 (2007). Hagenfeldt K. Contraception 6(1):37-54 (1972). Hannan NJ et al., Endocrinology 152(12):4948-4956 (2011). Holland MK, Pike IL., J Reprod Fertil 53(2):335-339 (1978). Jee BC et al., Fertil Steril 91(2):528-534 (2009). Jinno M et al., Fertil Steril 76(6):1168-1174 (2001). Karimzade MA et al., Arch Gynecol Obstet 281(3):499-503 (2010). Kasius A et al., Hum Reprod Update 20(4):530-541 (2014). Kelly WA et al., J Reprod Fertil 19(2):331-340 (1969). Lalitkumar S et al., Fertil Steril 100(4):1160-1169. doi:10.1016 / j.fertnstert.2013.06.023 (2013). Larsson B et al., Fertil Steril 36(6):734-736 (1981). Lavranos TC et al., J Reprod Fertil 105(2):331-338 (1995). Liang Y et al., Mediators Inflamm doi: 10.1155 / 2015 / 757184 (2015). Mao X et al., Fertil Steril 108(1):55-61.e1. doi:10.1016 / j.fertnstert.2017.05.014 (2017). Martin JS et al., Fertil Steril 64(1):98-102 (1995). Mikolajczyk M et al., Am J Reprod Immunol 58(1):65-74 (2007). Mitchell MH et al., Biol Reprod 67(2):460-464 (2002). Miwa I et al., Fertil Steril 91(4):998-1004 (2009). Moreno I et al., Am J Obstet Gynecol 215(6):684-703 (2016). Nastri CO et al., Cochrane Database Syst Rev 3:CD009517 (2015). Norwitz ER et al., N Engl J Med 345(19):1400-1408 (2001). Rafi A et al., Indian J Clin Biochem 28(2): 147-151. doi: 10.1007 / s12291-012-0240-9 (2013). Robertson SA, Sharkey DJ. Fertil Steril 106(3):511-519. doi: 10.1016 / j.fertnstert.2016.07.1101 (2016). Rockwell LC et al., Biol Reprod 67(6):1804-1810 (2002). Sadovsky E et al., Contraception 12(5):541-547 (1975). Schjenken JE, Robertson SA., Reprod Domest Anim 49 Suppl 3:27-36. doi: 10.1111 / rda.12383 (2014). Sengupta J et al., Contraception 74(5):419-425 (2006). Seo WS et al., Fertil Steril 95(8):2707-2710 (2011). Sheppard BL., Contraception 36(1):1-10 (1987). Siddiqi KS et al., Nanoscale Res Lett 13(1):141 (2018). Sigalos G et al., Hum Fertil (Camb) 20(1):3-13 (2017). Stanford JB, Mikolajczyk RT. Am J Obstet Gynecol 187(6):1699-1708 (2002). Stewart CL et al., Nature 359(6390):76-79 (1992). Timonen H. Contraception 14(1):25-38 (1976). Valbuena D et al., Fertil Steril 108(1):4-8. doi:10.1016 / j.fertnstert.2017.05.030 (2017). Vincent M et al., Int J Hyg Environ Health 219(7 PtA):585-591 (2016). Webb FT. J Reprod Fertil 32(3):429-439 (1973). Wu J et al., Contraception 85(5):509-518. doi: 10.1016 / j.contraception.2011.09.016 (2012). Yuan X et al., Reprod Biomed Online 33(2):197-205 (2016). Xin ZM et al., Zhonghua Fu Chan Ke Za Zhi 39(11):771-775 (2004). Zipper J et al., Int J Fertil 22(3):155-161 (1977).

Claims

1. A formulation comprising copper ions for use in enhancing embryo implantation in a subject, wherein the formulation is administered to the uterine cavity of the subject, wherein the copper ions are provided in solution or gel form, (i) wherein the subject is hoping to achieve pregnancy through natural conception, and the formulation is administered to the subject prior to ovulation and within the same menstrual cycle, or (ii) wherein the subject is undergoing treatment by assisted reproductive technology involving the transfer of embryo, and the formulation is administered to the subject prior to embryo transfer and within the same menstrual cycle, or (iii) wherein the subject is undergoing treatment by intra-uterine insemination (IUI), and the formulation is administered to the subject prior to IUI and within the same menstrual cycle, wherein the formulation is administered to the uterus cavity of the subject in an amount effective to stimulate endometrial production of leukaemia inhibitory factor (LIF) and / or vascular endothelial growth factor (VEGF), wherein the formulation provides copper ions to the uterine fluid in an amount in the range of 0.025 µg to 12.5 µg per administration.

2. The formulation for use according to claim 1, wherein the copper is provided in a biodegradable gel form or wherein biodegradable gel depots can be formed in situ within the uterus, wherein the copper is preferably formulated with hydroxyethyl cellulose and glycerol.

3. The formulation for use according to claim 1 or 2, wherein the formulation provides copper ions to the uterine fluid in an amount in the range of about 0.1 µg to about 10 µg per administration.

4. The formulation for use according to any one of the preceding claims, comprising inserting into the uterine cavity of the subject a device comprising the formulation comprising copper for a period no longer than 60 minutes.

5. The formulation for use according to claim 4, wherein the device has an elongated form and comprises a distal section and a proximal base section, and the step of inserting the device into the uterine cavity involves inserting at least a portion of the distal section into the uterine cavity, wherein the portion of the distal section that is inserted into the uterine cavity, or a part thereof, preferably comprises or preferably is provided with copper and elicits copper ions to stimulate endometrial production of LIF and / or VEGF, and wherein the device is preferably an embryo transfer catheter.

6. The formulation for use according to any one of the preceding claims, wherein the formulation is administered on multiple occasions during the time between the cessation of the menses and ovulation or commencement of the increase in progesterone that accompanies ovulation.