Compositions and methods for deep dermal drug delivery - Patents.com

Abstract

Pharmaceutical compositions for topical administration of drugs to the pilosebaceous unit and methods for administering the same. As disclosed herein, the inventors of the present invention have surprisingly discovered that pharmaceutical compositions containing small particles of an active pharmaceutical ingredient and a silicone, such as dimethicone or cyclomethicone, can be administered to the pilosebaceous unit. The pharmaceutical compositions can contain SHR0302 or spironolactone as the active pharmaceutical ingredient.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application claims priority to U.S. Provisional Application No. 63 / 114,887, filed November 17, 2020, and U.S. Provisional Application No. 63 / 221,349, filed July 13, 2021, the disclosures of which are incorporated by reference in their entirety into this specification.

[0002] FIELD OF THEINVENTION

[0002] The subject matter disclosed herein generally relates to pharmaceutical compositions for topical administration of drugs to the pilosebaceous unit and methods for administering the same. As disclosed herein, the inventors of the present invention have made a surprising discovery that pharmaceutical compositions comprising small particles of active pharmaceutical ingredient and silicone, such as dimethicone or cyclomethicone, can be targeted to the pilosebaceous unit. In a preferred embodiment, the pharmaceutical composition comprises SHR0302 or spironolactone as the active pharmaceutical ingredient. [Background technology]

[0003]

[0003] Transdermal and topical delivery of drugs have various advantages compared to other routes of administration. Transdermal and topical delivery can be used to continuously deliver drugs into the systemic circulation and avoid first-pass metabolism. In contrast, for oral drug delivery, there is a significant first-pass effect of the liver that can cause premature metabolism of the drug. Transdermal and topical delivery also have advantages over intravenous administration, which requires sterile products and can be painful, thereby increasing non-compliance by patients. On the other hand, transdermal delivery is not sterile, non-invasive, and can be self-administered.

[0004]

[0004] Traditional drug delivery systems have focused on administration via the transepidermal delivery route. Andrea C. Lauer et al., Transfollicular Drug Delivery, Pharmaceutical Research 12:2 (1995). Skin is composed of four main layers: (a) the stratum corneum (non-viable epidermis), (b) the viable epidermis, (c) the dermis, and (d) the subcutaneous tissue. Skin also contains appendages in the form of terminal hairs, which can extend more than 3 mm below the skin surface into the subcutaneous adipose tissue, and vellus hairs, which are thin and often unnoticed hairs that extend less than 1 mm into the dermis. The hair follicles, hair shafts, and sebaceous glands that secrete lubricating substances into the hair follicles comprise what is known as the pilosebaceous unit. Although the stratum corneum has traditionally been viewed as the primary route for the penetration of drugs, it is also the main barrier to transdermal absorption. In the past, researchers have questioned the importance of the pilosebaceous unit in drug delivery.

[0005]

[0005] More recently, however, the potential role of the pilosebaceous unit and alternative mechanisms for transdermal drug delivery have been investigated. Amit Verma et al., Transfollicular drug delivery: current perspectives, Research and Reports in Transdermal Drug Delivery (April 20, 2016). Mammalian hair follicles are complex and dynamic structures in which unique biochemical and immunological reactions occur. Although the pilosebaceous unit may be an acceptable target for drug delivery, several challenges exist for drug delivery to the pilosebaceous unit. One of the challenges for drug delivery to the pilosebaceous unit is the need to bypass the stratum corneum, which extends to a depth of approximately 10-20 μm, and the upper capillary network, which extends to a depth of approximately 80 μm. [Prior art documents] [Non-patent literature]

[0006] [Non-Patent Document 1] Andrea C. Lauer et al., Transfollicular Drug Delivery, Pharmaceutical Research 12:2 (1995) [Non-Patent Document 2] Amit Verma et al., Transfollicular drug delivery: current perspectives, Research and Reports in Transdermal Drug Delivery (April 20, 2016) Summary of the Invention

[0007]

[0006] Currently, there is a need for pharmaceutical compositions that can penetrate deeper into the dermis, approximately 1,000 μm to 2,000 μm to the pilosebaceous unit. There is an unmet need for new pharmaceutical compositions and methods of administering drugs via the pilosebaceous unit.

[0008] The present invention relates to a pharmaceutical composition for topical administration of drugs to the pilosebaceous unit and a method for administering the pharmaceutical composition. The inventors of the present invention have made a surprising discovery that a pharmaceutical composition comprising small particles of active pharmaceutical ingredient and silicone, such as dimethicone or cyclomethicone, can be delivered to the pilosebaceous unit, resulting in deeper penetration into the dermis and improved efficacy. In a preferred embodiment, the pharmaceutical composition comprises SHR0302 or spironolactone as the active pharmaceutical ingredient.

[0009] In certain embodiments of the present invention, a pharmaceutical composition is provided comprising a therapeutically effective amount of an active pharmaceutical ingredient and a silicone selected from the group consisting of dimethicone, cyclomethicone, and combinations thereof. The active pharmaceutical ingredient has a primary particle size distribution characterized by a D90 value of less than about 20 μm. In certain embodiments, the pharmaceutical ingredient has a primary particle size distribution characterized by a D90 value of less than about 10 μm or more preferably less than about 5 μm. In certain embodiments, the composition comprises about 0.10% w / w to about 7.5% w / w of the active pharmaceutical ingredient. The pharmaceutical composition of the present invention may be capable of delivering the active pharmaceutical ingredient to the pilosebaceous unit. In certain embodiments, the active pharmaceutical ingredient is capable of achieving at least 1 mm of skin penetration in a subject.

[0010]

[0009] In a particular embodiment of the present invention, a pharmaceutical composition is provided comprising a therapeutically effective amount of SHR0302 or a pharma- ceutically acceptable salt thereof. SHR0302 may have a primary particle size distribution characterized by a D90 value of less than about 20 μm, less than about 10 μm, or more preferably less than about 5 μm. SHR0302 may further have a primary particle size distribution characterized by a D50 value of less than about 5 μm, less than about 1 μm, or more preferably less than about 0.7 μm. SHR0302 may further have a primary particle size distribution characterized by a D10 value of less than about 1 μm, less than about 0.5 μm, or more preferably less than about 0.25 μm.

[0011]

[0010] The pharmaceutical composition further comprises a silicone selected from the group consisting of dimethicone, cyclomethicone, and combinations thereof. In certain embodiments of the present invention, the pharmaceutical composition comprises SHR0302 suspended in at least one of dimethicone and cyclomethicone.

[0012]

[0011] In certain embodiments, the pharmaceutical composition may contain from about 0.10% w / w to about 5% w / w of SHR0302 or a salt thereof. In preferred embodiments, the pharmaceutical composition may contain from about 0.1% w / w to about 3% w / w of SHR0302 or a salt thereof.

[0013]

[0012] In certain aspects of the present invention, a method for treating alopecia areata in a subject in need thereof is provided. The method comprises topically administering to the subject a pharmaceutical composition of SHR0302 as described herein. In the method of the present invention, SHR0302 or a salt thereof can be delivered to the pilosebaceous unit. In the method disclosed herein, administration of the pharmaceutical composition can result in transdermal penetration of SHR0302 to a depth of at least about 1 mm in the subject, preferably about 2-3 mm in the subject, of the hair bulb for terminal hair.

[0014]

[0013] In a particular embodiment of the present invention, a pharmaceutical composition is provided that comprises a therapeutically effective amount of spironolactone or its pharma- ceutically acceptable salt.Spironolactone can have a primary particle size distribution characterized by a D90 value of less than about 6 μm, less than about 1 μm, or more preferably less than about 0.25 μm.Spironolactone can further have a primary particle size distribution characterized by a D50 value of less than about 2.7 μm, less than about 0.75 μm, or more preferably less than about 0.15 μm.Spironolactone can further have a primary particle size distribution characterized by a D10 value of less than about 1.2 μm, less than about 0.50 μm, or more preferably less than about 0.10 μm.

[0015]

[0014] The pharmaceutical composition further comprises a silicone selected from the group consisting of dimethicone and cyclomethicone. In certain embodiments of the invention, the pharmaceutical composition of spironolactone is an oil-in-water emulsion.

[0016]

[0015] Additionally, the pharmaceutical composition may comprise from about 0.10% w / w to about 7.5% w / w of spironolactone or a salt thereof. In certain embodiments, the pharmaceutical composition may comprise from about 0.5% w / w to about 5% w / w of spironolactone or a salt thereof.

[0017]

[0016] In certain embodiments of the present invention, a method of treating acne in a subject in need thereof is provided. In certain embodiments, the subject is a human male or female. In a preferred embodiment, the subject is a female human. The method includes topically administering to the subject a pharmaceutical composition of spironolactone as described herein. In the methods of the present invention, spironolactone or a salt thereof can be delivered to the pilosebaceous unit. In the methods disclosed herein, administration of the pharmaceutical composition can result in skin penetration of spironolactone of at least 1 mm in the subject, preferably about 2 or 3 mm in the subject.

[0018] BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The accompanying drawings, which are incorporated in this specification and form a part of this disclosure, aid in explaining various aspects of the present invention and, together with the description, further serve to describe the present invention so as to enable those skilled in the relevant art to make and use the aspects disclosed herein. [Brief description of the drawings]

[0019] [Figure 1] FIG. 1 shows a particle size distribution plot of SHR0302 in an exemplary pharmaceutical composition. [Diagram 2] FIG. 2 shows the Fourier transform ion cyclotron resonance-high resolution-matrix assisted laser desorption / ionization mass spectrometry (FTICR-HR-MALDI) depth profile of 0.3% SHR0302 topical 30% DMSO cream for the first donor (Donor A). [Diagram 3]

[0020] FIG. 3 shows the FTICR-HR-MALDI depth profile of a 3% SHR0302 topical suspension in dimethicone for the first donor (Donor A). [Figure 4]

[0021] FIG. 4 shows the FTICR-HR-MALDI depth profile of 0.3% SHR0302 topical 30% DMSO cream for a second donor (Donor B). [Diagram 5]

[0022] FIG. 5 shows the FTICR-HR-MALDI depth profile of a 3% SHR0302 topical suspension in dimethicone for a second donor (Donor B). [Figure 6]

[0023] FIG. 6 shows the particle size distribution of spironolactone in a suspension of 5.0% nano-milled spironolactone in water with 0.05% dioctyl sulfosuccinate (DOSS) and 1.0% hydroxylpropylcellulose. [Figure 7]

[0024] FIG. 7 is a photomicrograph taken after two weeks of storage past the completion of milling of a 5% spironolactone suspension in cyclomethicone that had been roller milled to form a suspension having a D90 of about less than 5 μm. [Figure 8]

[0025] FIG. 8 shows the cumulative amount of spironolactone appearing in the receptor solution over 24 hours following a single 5.0 μl dose per cell (10 mg per cm2 of skin tissue) for two exemplary formulations (Formulation 1 and Formulation 2 described in Example 4) and a comparative gel formulation (also described in Example 4). [Figure 9]

[0026] FIG. 9 shows the amount of spironolactone (ng) in the epidermis and dermis after 24 hours for two exemplary formulations (Formulation 1 and Formulation 2 described in Example 4) and a comparative gel formulation (also described in Example 4). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0020]

[0027] Before the present invention is described in detail below, it should be understood that the present invention is not limited to the specific methodology, protocols, and reagents described herein, since these may vary. It should also be understood that the terminology used herein is for the purpose of describing specific embodiments only, and is not intended to limit the scope of the present invention, which will be limited only by the appended claims. Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by those skilled in the art to which this invention belongs.

[0021]

[0028] All publications, patents and patent applications cited herein are incorporated herein in their entirety by reference unless otherwise stated.When the same term is defined in the publication, patent or patent application incorporated herein by reference and in this disclosure, the definition in this disclosure represents the controlling definition.For publications, patents and patent applications that are referenced to describe a particular type of compound, chemistry, etc., the portion related to such compound, chemistry, etc. is the portion of the document that is incorporated herein by reference.

[0022]

[0029] It is noted that as used herein, the singular forms "a," "an," and "the" include plural references unless the context clearly dictates otherwise. Thus, for example, an "active ingredient" includes a single ingredient as well as two or more different ingredients, and a "sulfate" includes a single sulfate as well as two or more different sulfate salts.

[0023]

[0030] The term "about," when used in connection with a numerical value, is meant to encompass numerical values ​​in a range having a lower limit of 5% less than the stated numerical value and an upper limit of 5% greater than the stated numerical value.

[0024]

[0031] The term "effective" refers to an amount of a compound, agent, substance, combination or composition sufficient to result in a decrease in the severity of disease symptoms, an increase in the frequency and duration of disease symptom-free periods, or prevention of a disability or disorder due to disease affliction. Amounts can be alone or in combination with other compounds, agents or substances, as a single dose or according to a multiple dose regimen. One of skill in the art will be able to determine such amounts based on factors such as the size of the subject, the severity of the subject's symptoms, and the particular composition or route of administration selected.

[0025]

[0032] "Pharmaceutically acceptable" means generally safe for administration to humans or animals. Preferably, a pharma- ceutically acceptable component is one approved by a federal or state regulatory agency or listed in the United States Pharmacopeia, published by the United States Pharmacopeial Convention (Rockville, Md.), or other generally recognized pharmacopoeias, for use in animals, more particularly humans.

[0026]

[0033] A "pharmaceutical composition" according to the invention can be in the form of a composition in which different active ingredients and diluents and / or carriers are mixed with one another, or it can also take the form of a combined preparation in which the active ingredients are present in partially or completely different forms. An example of such a combination or combined preparation is a kit of parts.

[0027]

[0034] As used herein, the term "subject" or "patient" most preferably refers to a human. The term "subject" or "patient" can include any mammal that can benefit from the compounds described herein.

[0028]

[0035] A "therapeutic amount" or "therapeutically effective amount" is an amount of a therapeutic agent sufficient to achieve its intended purpose. The effective amount of a given therapeutic agent will vary depending on factors such as the nature of the agent, the route of administration, the size of the subject to receive the therapeutic agent, and the purpose of the administration. The effective amount in each individual case can be empirically determined by one of ordinary skill in the art according to established methods in the art.

[0029]

[0036] The term "topical" with respect to administration of a drug or composition refers to the application of such drug or composition to an external epithelial surface, including the skin or cornea. With respect to this application, application inside a body orifice where the mucosal surface does not contain pilosebaceous units, such as the mouth, vagina, or rectum, is not considered a topical application.

[0030]

[0037] As used herein, "treating" a disease or disorder, "treating" or "treatment" means accomplishing one or more of the following: (a) reducing the severity and / or duration of the disorder; (b) limiting or preventing the occurrence of symptoms characteristic of the disorder(s) being treated; (c) inhibiting the worsening of symptoms characteristic of the disorder(s) being treated; (d) limiting or preventing the recurrence of the disorder(s) in patients who previously had the disorder(s); and (e) limiting or preventing the recurrence of symptoms in patients who previously had symptoms related to the disorder(s).

[0031]

[0038] The abbreviation "w / w" expresses the relative concentrations of components in a composition on a "weight to weight" basis (i.e., percentages refer to percentages of total weight) rather than on a volumetric or other amount basis.

[0032]

[0039] The present invention relates to a pharmaceutical composition for topical administration of drugs to the pilosebaceous unit and a method for administering the same.The inventors of the present invention have surprisingly discovered that pharmaceutical compositions comprising small particles of active pharmaceutical ingredients in silicones such as dimethicone or cyclomethicone can be targeted to the pilosebaceous unit, resulting in deeper penetration into the dermis and improved efficacy.In a preferred embodiment, the pharmaceutical composition comprises SHR0302 or spironolactone as the active pharmaceutical ingredient.

[0033]

[0040] In certain embodiments of the present invention, a pharmaceutical composition is provided that includes a therapeutically effective amount of an active pharmaceutical ingredient and a silicone selected from the group consisting of dimethicone, cyclomethicone, and combinations thereof. In certain embodiments, the amount of the active pharmaceutical ingredient can range from about 0.01% w / w to about 10% w / w, or from about 0.01% w / w to about 5% w / w, or from about 0.1% w / w to about 3% w / w. Exemplary ranges are from about 0.01% w / w to about 10% w / w, or from about 0.01% w / w to about 7.5% w / w, or from about 0.01% w / w to about 5% w / w, or from about 0.1% w / w to about 3% w / w, or from about 1.0% w / w to about 3% w / w, or from about 0.3% w / w to about 3.0% w / w. For example, the pharmaceutical composition may contain any of the following w / w percentages of active pharmaceutical ingredient: 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 7%, 1.8%, 1.9%, 1.0%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 2.1%, 2.2%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 2.9%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6% , 3.7%, 3.8%, 3.9%, 4.0%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%, 4.6%, 4.7%, 4.8%, 4.9%, 5.0%, etc.

[0034]

[0041] In the pharmaceutical composition of the present invention, the active ingredient is present as small particles. The particle size of the drug can be evaluated using laser diffraction. Laser diffraction is recognized by standards and guidance organizations including ISO and ASTM, and is widely used to determine particle size distribution. In performing the evaluation, the sample is passed through a laser beam, which results in the laser light being scattered at a range of angles. A detector placed at a certain angle measures the intensity of the light scattered at that position. A mathematical model is then applied to generate the particle size distribution. The particle size values ​​reported herein are determined by using liquid or wet dispersion methods.

[0035]

[0042] In particle size determination, the median is defined as the value above which half of the population lies and below which half lies. In terms of particle size distribution, the median is called the D50. The D50 is the size that separates the distribution into upper and lower halves above this diameter. The distribution width can also be characterized by listing one, two, or three values ​​on the X-axis, typically some combination of D10, D50, and D90. The median, D50, is defined above as the diameter below which half of the population lies. Similarly, 90 percent of the distribution lies below the D90 and 10 percent of the population lies below the D10.

[0036]

[0043] In certain embodiments, the active pharmaceutical ingredient has a primary particle size distribution characterized by a D90 value of less than about 20 μm, less than about 15 μm, less than about 10 μm, or more preferably less than about 5 μm. In certain embodiments, the active pharmaceutical ingredient has a primary particle size characterized by a D90 value of about 0.001 μm, 0.01 μm, or 0.1 μm to about 5 μm, 10 μm, 15 μm, and 20. The active pharmaceutical ingredient may further have a primary particle size distribution characterized by a D50 value of less than about 5 μm, less than about 2 μm, less than about 1 μm, less than about 0.8 μm, or more preferably less than about 0.7 μm. In certain embodiments, the active pharmaceutical ingredient has a primary particle size characterized by a D50 value of about 0.001 μm, 0.01 μm, or 0.1 μm to about 0.7 μm, 0.80 μm, 1.0 μm, 2.0 μm, or 5.0 μm. The active pharmaceutical ingredient may further have a primary particle size distribution characterized by a D10 value of less than about 1 μm, less than about 0.5 μm, less than about 0.4 μm, or more preferably less than about 0.25 μm. In certain embodiments, the active pharmaceutical ingredient has a primary particle size characterized by a D10 value of about 0.0001 μm, 0.001 μm, or 0.01 μm to about 0.25 μm, 0.4 μm, 0.5 μm, or 1.0 μm.

[0037]

[0044] In certain embodiments, the pharmaceutical compositions of the present invention are capable of delivering an active pharmaceutical ingredient to the pilosebaceous unit, hi certain embodiments, the active pharmaceutical ingredient is capable of achieving at least 1 mm of skin penetration in a subject.

[0038]

[0045] In certain embodiments of the present invention, the pharmaceutical composition comprises (3aR,5S,6aS)-N-(3-methoxyl-1,2,4-thiadiazol-5-yl)-5-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxamide, a JAK1 inhibitor also known as SHR0302 or ARQ-250. The terms SHR0302 and ARQ-250 are used interchangeably herein. The structure of SHR0302 is as follows:

[0039] [ka]

[0040] .

[0041]

[0046] SHR0302 is a potent small molecule inhibitor of JAK1 that has been shown to be selectively selective for JAK1 over JAK2, and therefore has the potential to treat inflammatory diseases without causing the deleterious effects of hematopoiesis, such as anemia, thrombocytopenia, and neutropenia, associated with JAK2 inhibition. SHR0302 is disclosed in U.S. Patent No. 9,527,851, which is incorporated herein by reference.

[0042]

[0047] In certain embodiments of the invention, the pharmaceutical composition comprises 17-hydroxy-7α-mercapto-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone acetate, an aldosterone agonist also known as spironolactone. The structure of spironolactone is as follows:

[0043] [ka]

[0044]

[0048] Spironolactone is a drug that acts at the mineralocorticoid receptor level by competitively inhibiting the binding of aldosterone. This steroid compound has been used to block aldosterone-dependent sodium transport in the distal tubules of the kidney to reduce edema and to treat essential hypertension and primary hyperaldosteronism. Orally administered spironolactone is also effective in treating women with acne. EM Attwa et al., Efficacy and safety of topical spironolactone 5% gel versus placebo in the treatment of acne vulgaris, J. Dermatol. Venerol. 39:89-94 (2019); JW Charny et al., Spironolactone for the treatment of acne in women, a retrospective study of 110 patients, Int. J. Womens Dermatol. 3(2): 111-115 (2017). Spironolactone is commercially available under the trade names ALDACTONE® and CAROSPIR®. Spironolactone is disclosed in U.S. Patent No. 3,013,012, which is incorporated herein by reference.

[0045]

[0049] In the present invention, the pharmaceutical composition is administered locally.The pharmaceutical composition can contain SHR0302 or spironolactone as free base or pharmaceutically acceptable salt.Suitable pharmaceutically acceptable salts can be found in Remington's Pharmaceutical Sciences, 17th Edition, Mack Publishing Company (1985), which is incorporated herein by reference.

[0046]

[0050] In certain embodiments, the pharmaceutical composition comprises SHR0302 having a primary particle size distribution characterized by a D90 value of less than about 20 μm, less than about 15 μm, less than about 10 μm, or more preferably less than about 5 μm. In certain embodiments, SHR0302 has a primary particle size characterized by a D90 value of about 0.01 μm, 0.1 μm, or 1.0 μm to about 5.0 μm, 10.0 μm, 15.0 μm, or 20.0 μm.

[0047]

[0051] SHR0302 may further have a primary particle size distribution characterized by a D50 value of less than about 5 μm, less than about 2 μm, less than about 1 μm, less than about 0.8 or more preferably less than about 0.7 μm. In certain embodiments, SHR0302 has a primary particle size characterized by a D50 value of about 0.001 μm, 0.01 μm or 0.1 μm to about 0.7 μm, 0.8 μm, 1.0 μm, 2.0 μm or 5.0 μm.

[0048]

[0052] SHR0302 may further have a primary particle size distribution characterized by a D10 value of less than about 1 μm, less than about 0.5 μm, less than about 0.4 μm, or more preferably less than about 0.25 μm. In certain embodiments, SHR0302 has a primary particle size characterized by a D10 value of about 0.0001 μm, 0.001 μm, or 0.01 μm to about 0.25 μm, 0.4 μm, 0.5 μm, or 1.0 μm.

[0049]

[0053] In certain embodiments, the pharmaceutical composition comprises spironolactone having a primary particle size distribution characterized by a D90 value of less than about 6 μm, less than about 5 μm, less than about 2 μm, less than about 1 μm, less than about 0.5 μm, less than about 0.25 μm, or more preferably less than about 0.2 μm. In certain embodiments, the spironolactone has a primary particle size characterized by a D90 value of about 0.001 μm, 0.01 μm, or 0.1 μm to about 0.2 μm, 0.25 μm, 0.5 μm, 1 μm, 2 μm, 5 μm, or 6 μm.

[0050]

[0054] The spironolactone may further have a primary particle size distribution characterized by a D50 value of less than about 2.7 μm, less than about 2.0 μm, less than about 1.0 μm, less than about 0.75 μm, 0.5 μm, less than about 0.25 μm, less than about 0.2 μm, or more preferably less than about 0.15 μm. In certain embodiments, the spironolactone has a primary particle size characterized by a D50 value of about 0.001 μm, 0.01 μm, or 0.1 μm to about 0.15 μm, 0.2 μm, 0.25 μm, 0.5 μm, 0.75 μm, 1.0 μm, 2.0 μm, or 2.7 μm.

[0051]

[0055] The spironolactone may further have a primary particle size distribution characterized by a D10 value of less than about 1.2 μm, less than about 1.0 μm, less than about 0.5 μm, less than about 0.25 μm, less than about 0.15 μm, less than about 0.10 μm, or more preferably less than about 0.08 μm. In certain embodiments, the spironolactone has a primary particle size characterized by a D10 value of about 0.0001 μm, 0.001 μm, or 0.01 μm to about 0.10 μm, 0.15 μm, 0.25 μm, 0.5 μm, 1.0 μm, or 1.2 μm.

[0052]

[0056] The pharmaceutical composition of the present invention further comprises a silicone selected from the group consisting of dimethicone, cyclomethicone or a combination thereof. Dimethicone, also known as polydimethylsiloxane (PDMS), is a polymerizable organosilicon compound. Cyclomethicone is a group of methylsiloxanes, which, unlike dimethicone, is a cyclic organosilicon compound. In certain embodiments, the pharmaceutical composition can comprise a combination of silicones, including dimethicone and cyclomethicone. For example, the pharmaceutical composition can comprise dimethicone-cyclomethicone-dimethicone / vinyl dimethicone. Additional methylsiloxane compatible excipients, such as cyclopentasiloxane, dimethiconol and phenyl trimethicone, can be added to dimethicone and / or cyclomethicone to adjust aesthetics or viscosity. Silicones, such as dimethicone or cyclomethicone, have a polarity similar to sebum, allowing the pharmaceutical composition to target hair follicle delivery.

[0053]

[0057] In certain embodiments, the pharmaceutical composition is a suspension, in which the active ingredient (e.g., SHR0302 or spironolactone) is suspended in a silicone (e.g., dimethicone or cyclomethicone).In certain embodiments, the pharmaceutical composition can be formulated as an emulsion.For example, the pharmaceutical composition can be formulated in one of the following forms:

[0058] Oil-in-water emulsions: The product can be an emulsion that contains a separate phase of hydrophobic components and a continuous aqueous phase that contains water and optionally one or more polar hydrophilic excipients as well as solvents, co-solvents, salts, surfactants, emulsifiers and other components. These emulsions can contain water-soluble or water-swellable polymers that help stabilize the emulsion.

[0054]

[0059] Water-in-oil emulsions: The compositions can be emulsions that contain a continuous phase of hydrophobic components and an aqueous phase that contains water and optionally one or more polar hydrophilic carrier(s) and salts or other components. These emulsions can contain oil-soluble or oil-swellable polymers and one or more emulsifier(s) that help stabilize the emulsion.

[0055]

[0060] Microemulsions: These are clear, thermodynamically stable, isotropic liquid systems that contain oil, water, and surfactants, often in combination with cosurfactants. Microemulsions can be water-continuous, oil-continuous, or bicontinuous mixtures. Formulations can also optionally contain up to 60% water by weight. Higher levels may be appropriate in some compositions.

[0056]

[0061] Nanoemulsions: These are isotropic dispersion systems containing water, oil, and emulsifiers. The systems can be oil-in-aqueous systems or aqueous systems dispersed in oil systems forming nanometer-sized droplets or oily phases. Nanoemulsions often have a higher loading capacity for lipophilic active ingredients than microemulsions. Hydrophobic and hydrophilic active ingredients can also be incorporated into nanoemulsions. Nanoemulsions can be formed by any suitable method known in the art, including high pressure homogenization, microfluidization, and phase transition temperatures.

[0057]

[0062] In certain embodiments, the pharmaceutical composition consists essentially of an active ingredient and a silicone selected from the group consisting of dimethicone, cyclomethicone, or a combination thereof. Alternatively, the pharmaceutical composition can be formulated with additional components, including those traditionally found in cosmetic and medicinal topical products.

[0058]

[0063] Administration and Dosage

[0064] The present invention includes a method of treating hair loss conditions, such as alopecia, androgenetic alopecia, hypothrichosis, and telogen effluvium, which can include treating the hair loss condition in a patient in need thereof by administering to the patient a composition of SHR0302 or spironolactone as described herein.

[0059]

[0065] In a preferred embodiment, the present invention comprises a method for treating alopecia areata (AA). AA is one of the most prevalent autoimmune diseases, resulting in hair loss due to the breakdown of immune privilege of hair follicles and subsequent autoimmune destruction. AA is a skin disease that causes hair loss on the scalp and elsewhere. Prior to the present invention, topical administration of JAK inhibitors has not shown reproducible clinical efficacy. Without being bound by theory, it is believed that the failure of JAK inhibitors to treat AA prior to the present invention as claimed is due to insufficient drug delivery to the pilosebaceous unit, more specifically to the hair bulb. The inventors of the present invention have made the surprising discovery that the pharmaceutical compositions disclosed herein can penetrate at least about 1 mm, at least about 2 mm, and at least about 3 mm into the hair follicle of AA patients.

[0060]

[0066] In certain embodiments, the present invention provides a method for treating AA in a patient in need thereof, comprising topically applying to the patient a therapeutically effective amount of a SHR0302 pharmaceutical composition as described herein. In certain embodiments, the active ingredient, SHR0302, may be administered in a therapeutically effective amount. In certain embodiments, the amount of SHR0302 may range from about 0.01% w / w to about 7.5% w / w, or from about 0.01% w / w to about 5% w / w, or from about 0.1% w / w to about 3% w / w. Exemplary ranges are from about 0.01% w / w to about 5% w / w, or from about 0.01% w / w to about 3% w / w, or from about 0.1% w / w to about 3% w / w, or from about 0.3% w / w to about 3.0% w / w. For example, topical formulations may contain any of the following w / w percentages of SHR0302: 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 7%, 1.8%, 1.9%, 1.0%, 2.1%, and 2.2%. 2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6% , 3.7%, 3.8%, 3.9%, 4.0%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%, 4.6%, 4.7%, 4.8%, 4.9%, 5.0%, etc.

[0061]

[0067] The present invention further provides a method for treating acne in a patient in need thereof. Acne is a disorder of the pilosebaceous unit located on face, chest and back. Acne can be one selected from the group consisting of acne, acne vulgaris, inflammatory acne, non-inflammatory acne, flash acne, nodular papulopustular acne, confluent acne, acne rosacea, rosacea, exfoliative acne, adult onset acne, persistent recurrent acne after teenage years and acne associated with other disorders. In certain embodiments, the patient is a human male or female patient. In a preferred embodiment, the patient is a human female. In addition, patients: (a) experience acne flares that cycle with menstruation; (b) suffer from adult-onset acne or persistent recurrent acne beyond the teenage years, even in the absence of clinical or laboratory signs of hyperandrogenism; (c) use oral contraceptives and exhibit moderate to severe acne, especially with a clinically hormonal pattern; or (d) have not responded to conventional therapy and are not candidates for oral isotretinoin therapy.

[0062]

[0068] In certain embodiments, the present invention provides a method for treating acne in a patient in need thereof, comprising topically applying to the patient a therapeutically effective amount of a spironolactone pharmaceutical composition as described herein. In certain embodiments, the active ingredient spironolactone may be administered in a therapeutically effective amount. In certain embodiments, the amount of spironolactone may range from about 0.01% w / w to about 10% w / w, or from about 0.01% w / w to about 7.5% w / w, or from about 0.01% w / w to about 5% w / w, or from about 0.1% w / w to about 3% w / w. Exemplary ranges are from about 0.1% w / w to about 10% w / w, or from about 0.1% w / w to about 7.5% w / w, or from about 0.1% w / w to about 5% w / w, or from about 0.1% w / w to about 3% w / w, or from about 1.0% w / w to about 5% w / w, or from about 0.3% w / w to about 5.0% w / w. For example, topical formulations may contain spironolactone in any of the following w / w percentages: 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 7%, 1.8%, 1.9%, 1.0%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%. , 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4.0%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%, 4.6%, 4.7%, 4.8%, 4.9%, 5.0%, 5.1%, 5.2%, 5.3%, 5.4%, 5. 5%, 5.6%, 5.7%, 5.8%, 5.9%, 6.0%, 6.1%, 6.2%, 6.3%, 6.4%, 6.5%, 6.6%, 6.7%, 6.8%, 6.9%, 7.0%, 7.1%, 7.2%, 7.3%, 7.4%, 7.5%, etc.

[0063]

[0069] In certain embodiments, the pharmaceutical composition is administered topically as a regimen, such as at regular intervals. For example, the topical pharmaceutical composition can be administered once a day, twice a day, three times a day, once a week, twice a week, three times a week, or four times a week. The pharmaceutical composition can be administered for a predetermined period of time. For example, the topical pharmaceutical composition can be administered for a period of about 2 weeks to at least about 6 months, or until an improvement in the skin condition or disease is visually observed. Exemplary periods for treatment regimens include 2 weeks, 1 month, 6 weeks, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, or 1 year. In a preferred embodiment, the topical pharmaceutical composition is administered 2 or 3 times daily for a period of at least 3 months, 4 months, 5 months, or 6 months.

[0064]

[0070] The following examples illustrate certain aspects of the invention without limiting them. EXAMPLES

[0065]

[0071] While various embodiments have been described above, it should be understood that they have been presented by way of example only, and not limitation. Thus, the breadth and scope of the present disclosure should in no way be limited by any of the exemplary embodiments described above. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the present disclosure unless otherwise indicated herein or otherwise clearly contradicted by context.

[0066]

[0072] Comparative Example 1

[0073] Comparative Example 1 was prepared as a 0.3% SHR0302 topical cream having the composition shown in Table 1.

[0067] [Table 1]

[0068]

[0074] Example 1

[0075] A pharmaceutical composition was prepared containing 3% SHR0302 suspended in dimethicone. The SHR0302 used in the composition had a particle size distribution as shown in Figure 1. The primary particle size distribution of SHR0302 is characterized by a D10 value of less than about 0.25 μm; a D50 value of less than about 0.7 μm; and a D90 value of less than about 5 μm. The pharmaceutical composition was a clear solution because the particles were too small to scatter visible light. A Malvern Metasizer Model 3000 using a Hydro MV dispersion unit was used to determine the particle size distribution profile of SHR0302. The sample preparation procedure performed was as follows: weigh 10-20 mg of SCP-treated ARQ-250 in a 30 mL vial, add 20 mL of ethyl acetate, sonicate the suspension with an ultrasonic probe at 40% power for 2 min in a 5 °C water bath, and transfer the sample suspension to a Malvern Hydro MV dispersion unit to obtain 5-15% obscuration. The instrument parameters were as follows: (i) refractive index of particles: 1.5; (ii) refractive index of dispersant 1.395; (iii) absorption index: 0.01; (iv) measurement duration: 10 s; (v) number of measurements: 3; (vi) stirring speed: 3500 rpm; (vii) ultrasonic: off.

[0069]

[0076] Example 2

[0077] The ability of Comparative Example 1 and Example 1 to penetrate into human cadaver scalp skin was evaluated. Two different human cadaver scalp skins (Donors A and B) were mounted on special tension cells. A dose (7.5 μL) of either Comparative Example 1 or Example 1 was applied to the scalp skin specimens for 6 hours. All formulation residues were washed off from the skin. 8 mm punch biopsies were taken from the dermal side of the skin and flash frozen in liquid nitrogen. Serial 10 μm frozen sections were taken, every other section was prepared for hematoxylin and eosin (H&E) staining, and adjacent sections were retained for analysis using Fourier transform ion cyclotron resonance-high resolution-matrix assisted laser desorption / ionization mass spectrometry (FTICR-HR-MALDI). FTICR-HR-MALDI analysis was performed using a Bruker 7T FTICR-HR-MALDI MS system.

[0070]

[0078] Figures 2 and 4 show the FTICR-HR-MALDI depth profiles of 0.3% SHR0302 topical 30% DMSO cream for Donor A and Donor B, respectively. As shown in Figure 2, Comparative Example 1 achieved maximum dermal penetration of less than 160 μm in Donor A. As shown in Figure 4, Comparative Example 1 achieved maximum dermal penetration of less than 500 μm in Donor B. The results are consistent with a pharmaceutical composition capable of delivering drug across the stratum corneum, indicating that the drug has not penetrated below the upper capillary network.

[0071]

[0079] Figures 3 and 5 show the FTICR-HR-MALDI depth profiles of 3% SHR0302 topical suspension in dimethicone for Donor A and Donor B, respectively. As shown in Figures 3 and 5, Example 1 achieved maximum skin penetration of more than 1 mm. The results surprisingly show that the pharmaceutical composition is capable of delivering drugs to the hair bulb.

[0072]

[0080] Example 3

[0081] A 50 mg / mL aqueous suspension of 5% spironolactone containing 0.5% dioctyl sodium sulfosuccinate and 1% hydroxypropylcellulose was successfully nanomilled to provide stable submicron particles of drug particle suspension after 2 weeks storage at 5° C. and ambient light. The spironolactone had a particle size distribution as shown in FIG. 6. A Horiba Laser Scattering Particle Size Distribution Analyzer Model LA-950 was used to determine the volume-based distribution profile of spironolactone. Circulation, stirring, and ultrasound were all turned off and the instrument was set to manual repeat mode.

[0073]

[0082] A stable 0.3% spironolactone oil-in-water emulsion was prepared having the composition shown in Table 2:

[0083]

[0074] [Table 2]

[0075]

[0084] Example 4

[0085] A 5.0%-5.5% spironolactone suspension in water containing 0.05%-0.055% dioctyl sodium sulfosuccinate and 1.0-1.1% hydroxylpropylcellulose was nanomilled to achieve the particle size distribution shown in Figure 6. The composition of the finished suspension is listed in Table 3 as Formulation 1. A 5% spironolactone suspension in cyclomethicone was roller milled to form a suspension with a D90 of approximately less than 5 μm, as shown in Figure 7 (micrograph taken after storage for 2 weeks past completion of milling). The composition of this finished suspension is listed in Table 3 as Formulation 2. A comparative gel formulation described in the literature was prepared and is listed in Table 3 as the comparative gel. (Attwa EM, Ibrahim AM, Abd El-Halim MF, Mahmoud HM, Efficacy and safety of topical spironolactone 5% gel versus placebo in the treatment of acne vulgaris, Egypt J Dermatol Venerol (2019); 39:89-94.)

[0086]

[0076] [Table 3]

[0077]

[0087] An in vitro skin penetration test (IVPT) was used to determine how rapidly different formulations cross excised human skin. Human cadaveric skin was sourced from two donors (Caucasian female, age = 48 years, abdominal skin harvest resulting in an average thickness of 580 μm; and Hispanic male, age = 50 years, abdominal skin harvest resulting in an average thickness of 910 μm). Dermatomal skin was received frozen from a US tissue bank and stored at -20°C until use. Skin was measured in sections of 0.503 cm 2The IVPT samples were loaded onto a vertical Franz cell with a diffusion area of ​​1.5 mm (8 mm diameter) and a receptor chamber filled with 3.0 ml of 4% BSA in water containing 0.01% gentamicin sulfate thermostated at 32°C. Five microliters of each formulation was administered to each Franz cell using a positive displacement pipette (10 mg per square centimeter of skin). The receptor solutions were analyzed using a validated LC-MS / MS (Kinetex C18, 5 μm, 2.1×50 mm column, Shimadzu LC20ADXR pump and AB Sciex API 4000 Turbo Spray detector). The cumulative amount of spironolactone assayed in the receptor solution is the average of four replicate IVPT measurements.

[0078]

[0088] To determine the levels of spironolactone retained in the epidermis and dermis 24 hours after application to the skin, all unabsorbed and unpenetrated spironolactone was washed from the skin surface. This was accomplished by wiping the tissue surface three times with a Q-tip wetted with 1xPBS, followed by two tape strips. The epidermis (including the stratum corneum) was peeled from the dermis and immersed in 4.0 ml of DMSO / acetonitrile (ACN) (50 / 50 v / v) mixture on an orbital shaker overnight at room temperature. The remaining dermal layer was cut into small pieces and extracted with 4.0 ml of DMSO / ACN mixture on an orbital shaker overnight at room temperature. The dermal and epidermal extracts were analyzed using a validated LC-MS / MS (Kinetex C18, 5 μm, 2.1 × 50 mm column, Shimadzu LC20ADXR pump and AB Sciex API 4000 Turbo Spray detector).

[0079]

[0089] FIG. 8 shows the results of the 5.0 μl per cell (1 cm of skin tissue) for Formulation 1, Formulation 2 and the comparative gel. 2FIG. 8 illustrates the cumulative amount of spironolactone appearing in the receptor solution over 24 hours after a single dose of 10 mg per 1000 μg of spironolactone ... High levels of API in the epidermis and dermis indicate that spironolactone targets the pilosebaceous unit and has significantly greater follicular deposition from the aqueous suspension (D90<0.5 μm, formulation 1) and the cyclomethicone suspension (D90<5.0 μm, formulation 2).

[0080]

[0090] The foregoing description has been presented for purposes of illustration and description. It is not intended to limit the invention to the precise form disclosed. Those skilled in the art will recognize that modifications and substitutions to the description of the basic invention may be made. This specification includes the disclosure of the following inventions. [Item 1] A pharmaceutical composition comprising the following: a therapeutically effective amount of SHR0302 or a pharma- ceutically acceptable salt thereof, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 20 μm; and Silicones selected from the group consisting of dimethicone and cyclomethicone 23. A pharmaceutical composition comprising: [Item 2] The pharmaceutical composition according to item 1, wherein the composition is a suspension. [Item 3] The pharmaceutical composition according to item 1, wherein the composition comprises about 0.10% w / w to about 5% w / w of SHR0302 or a salt thereof. [Item 4] The pharmaceutical composition according to item 1, wherein the primary particle size distribution of SHR0302 is characterized by a D90 value of less than about 10 μm. [Item 5] The pharmaceutical composition according to item 1, wherein the primary particle size distribution of SHR0302 is characterized by a D90 value of less than about 5 μm. [Item 6] The pharmaceutical composition according to item 1, wherein the primary particle size distribution of SHR0302 is characterized by a D50 value of less than about 1.0 μm. [Item 7] The pharmaceutical composition according to item 1, wherein the primary particle size distribution of SHR0302 is characterized by a D10 value of less than about 0.50 μm. [Item 8] A method for treating alopecia areata in a subject in need thereof, comprising: administering to the subject: (a) a therapeutically effective amount of SHR0302, or a pharma- ceutically acceptable salt thereof, wherein a primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 20 μm; and (b) a silicone selected from the group consisting of dimethicone and cyclomethicone. topically administering a pharmaceutical composition comprising The method includes: [Item 9] The method according to item 8, wherein the SHR0302 is delivered to the pilosebaceous unit. [Item 10] The method according to item 8, wherein the SHR0302 achieves skin penetration of at least 1 mm in the subject. [Item 11] The method according to item 8, wherein the pharmaceutical composition is a suspension. [Item 12] The method according to Item 8, wherein the composition comprises about 0.10% w / w to about 5% w / w of SHR0302 or a salt thereof. [Item 13] The method according to item 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 10 μm. [Item 14] The method according to item 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 5 μm. [Item 15] The method according to item 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D50 value of less than about 1.0 μm. [Item 16] The method according to item 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D10 value of less than about 0.50 μm. [Item 17] A pharmaceutical composition comprising the following: a therapeutically effective amount of an active pharmaceutical ingredient, the active pharmaceutical ingredient having a primary particle size distribution characterized by a D90 value of less than about 20 μm; and Silicones selected from the group consisting of dimethicone and cyclomethicone 23. A pharmaceutical composition comprising: [Item 18] The pharmaceutical composition according to Item 17, wherein the composition comprises about 0.10% w / w to about 5% w / w of an active pharmaceutical ingredient. [Item 19] The pharmaceutical composition according to item 17, wherein the primary particle size distribution of the active pharmaceutical ingredient is characterized by a D90 value of less than about 10 μm. [Item 20] The pharmaceutical composition according to item 17, wherein the primary particle size distribution of the active pharmaceutical ingredient is characterized by a D90 value of less than about 5 μm. [Item 21] The pharmaceutical composition according to item 17, wherein the active pharmaceutical ingredient is delivered to the pilosebaceous unit. [Item 22] The pharmaceutical composition according to item 17, wherein the active pharmaceutical ingredient is capable of achieving skin penetration of at least 1 mm in the subject.

Claims

1. 1. A pharmaceutical composition comprising: a therapeutically effective amount of SHR0302 or a pharma- ceutically acceptable salt thereof, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 20 μm; and Silicones selected from the group consisting of dimethicone and cyclomethicone 23. A pharmaceutical composition comprising:

2. 10. The pharmaceutical composition of claim 1, wherein the composition is a suspension.

3. 2. The pharmaceutical composition of claim 1, wherein the composition comprises about 0.10% w / w to about 5% w / w of SHR0302 or a salt thereof.

4. 2. The pharmaceutical composition of claim 1, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 10 μm.

5. 2. The pharmaceutical composition of claim 1, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 5 μm.

6. 2. The pharmaceutical composition of claim 1, wherein the primary particle size distribution of SHR0302 is characterized by a D50 value of less than about 1.0 μm.

7. 2. The pharmaceutical composition of claim 1, wherein the primary particle size distribution of the SHR0302 is characterized by a D10 value of less than about 0.50 μm.

8. 1. A pharmaceutical composition for use in a method of treating alopecia areata in a subject in need thereof, comprising: The pharmaceutical composition comprises: (a) a therapeutically effective amount of SHR0302 or a pharma- ceutically acceptable salt thereof, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 20 μm; and (b) a silicone selected from the group consisting of dimethicone and cyclomethicone. and administered topically to a subject. Pharmaceutical compositions.

9. 9. The pharmaceutical composition of claim 8, wherein the SHR0302 is delivered to the pilosebaceous unit.

10. 9. The pharmaceutical composition of claim 8, wherein said SHR0302 achieves a skin penetration of at least 1 mm in said subject.

11. 9. The pharmaceutical composition of claim 8, wherein the pharmaceutical composition is a suspension.

12. 9. The pharmaceutical composition of claim 8, wherein the composition comprises about 0.10% w / w to about 5% w / w of SHR0302 or a salt thereof.

13. 9. The pharmaceutical composition of claim 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 10 μm.

14. 9. The pharmaceutical composition of claim 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D90 value of less than about 5 μm.

15. 9. The pharmaceutical composition of claim 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D50 value of less than about 1.0 μm.

16. 9. The pharmaceutical composition of claim 8, wherein the primary particle size distribution of the SHR0302 is characterized by a D10 value of less than about 0.50 μm.

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