MEK inhibitors for the treatment of hantavirus infections

Abstract

The present invention relates to MEK inhibitors that can exhibit one or more beneficial therapeutic effects and can be used in the prevention and / or treatment of hantavirus infections.

Description

[Background technology]

[0001] Background of the Invention Hantaviruses (or orthohantaviruses) are single-stranded, enveloped, negative-strand RNA viruses in the Hantaviridae family of the Bunyavirales order. To date, 28 pathogenic hantavirus species are known. Hantavirus species vary depending on their geographic location. In Europe, the common hantavirus is Puumala virus, while in the Americas, Andes virus and Sin Nombre virus are common. In Asia, Seoul virus and Hantan virus are found. The natural hosts of hantaviruses are rodents, shrews, and bats, but clinical symptoms are not seen in the natural hosts. Hantavirus species are primarily transmitted via aerosolized rodent excreta (urine, saliva, and feces), but human-to-human transmission of Andes viruses was reported in South America in 2005 and 2019 (Martinez VP, Bellomo C, San Juan J, Pinna D, Forlenza R, Elder M, Padula PJ (2005). "Person-to-person transmission of Andes virus". Emerging Infectious Diseases; 11 (12): 1848-1853). For hantavirus species, the incubation period in humans can last up to several weeks.

[0002] Hantavirus infections are associated with high mortality rates and very limited treatment options are available, making these infections a global threat. In humans, hantavirus infections manifest in two clinical manifestations: hantavirus hemorrhagic fever with renal syndrome (HFRS), which has a 12% mortality rate, and hantavirus pulmonary syndrome (HPS), which has a 40% mortality rate. The severity of the disease depends on the causative hantavirus species and viral load. For example, severe disease courses are known to be caused by hantaviruses, Dobrava-Belgredo viruses, Sin Nombre viruses, and Andes viruses, while more moderate disease courses are more likely in, for example, Puumala viruses or Saaremaa viruses. At least 100,000 HFRS cases are recorded annually. In 2004, China alone recorded 40,000–60,000 cases per year (Zhang et al. 2004, Lee et al. 1996, Lee et al. 1998), compared with approximately 9,000 cases in Europe (Vapalahti et al. 2003, Heyman et al. 2009, Heyman et al. 2011).

[0003] Currently, there are no vaccines or antiviral drugs approved by the FDA or WHO for the treatment or prevention of hantavirus infection. A vaccine known as Hantavax has been under investigation since 1990 and is used in South Korea, but it has not yet been publicly approved and has limited efficacy. Killed virus vaccines have not been pursued due to the risks associated with mass production under tight confinements and unresolved questions about vaccine efficacy. Many laboratories are working toward vaccines that deliver viral antigens via DNA vectors or as recombinant proteins, but to date, none of these vaccines have been shown to be effective.

[0004] In addition, there are no approved treatments for HPS or HFRS other than alleviating the symptoms of the disease. The only drug that may be used is ribavirin, but its effectiveness is still unknown. One problem with the control of RNA viruses, such as hantaviruses, in particular, is the adaptability of the virus due to the high error rate of the viral polymerase, which makes it very difficult to produce suitable vaccines and develop antiviral substances. Most known antiviral drugs are therefore known to lead to resistance in individual RNA virus species.

[0005] Due to their very small genomes and therefore limited coding capacity for functions necessary for replication, all viruses are highly dependent on the functions of their host cells. Influencing such cellular functions necessary for viral replication can negatively affect viral replication in infected cells. In this scenario, viruses have no possibility of substituting missing cellular functions by adaptation, particularly by mutation, to escape selective pressure. This has already been shown for influenza A viruses by relatively nonspecific inhibitors of cellular kinases and methyltransferases (Scholtissek and Muller, Arch Virol 119, 111-118, 1991).

[0006] It is known in the art that cells have numerous signal transduction pathways that transmit signals to the cell nucleus, allowing cells to respond to external stimuli and to respond by cell proliferation, cell activation, differentiation, or controlled cell death. What these signal transduction pathways have in common is that they contain at least one kinase that transmits a signal after being activated by phosphorylating at least one protein. Observation of the cellular processes induced after viral infection has revealed that many DNA and RNA viruses selectively activate a well-defined signal transduction pathway, the so-called Raf / MEK / ERK kinase signal transduction pathway, in infected host cells (Benn et al., J Virol 70, 4978-4985, 1996; Bruder and Kovesdi, J Virol 71, 398-404, 1997; Popik and Pitha, Virology 252, 210-217, 1998; Rodems and Spector, J Virol 72, 9173-9180, 1998). This signal transduction pathway is one of the most important signal transduction pathways in cells and plays a key role in proliferation and differentiation processes. Growth factor-induced signals are transmitted by sequential phosphorylation from the serine / threonine kinase Raf to the dual-specificity kinase MEK (MAP kinase kinase / ERK kinase) and finally to the kinase ERK (extracellular signal-regulated kinase). MEK is the only known kinase substrate of Raf, and ERK isoforms have been identified as the only substrates of MEK. However, ERK can phosphorylate numerous substrates, including transcription factors that directly affect cellular gene expression (Cohen, Trends in Cell Biol 7, 353–361, 1997; Robinson and Cobb, Curr. Opin. Cell Biol 9, 180–186, 1997; Treisman, Curr. Opin. Cell Biol 8, 205–215, 1996).

[0007] In view of the prior art, it is apparent that there is a need for additional compounds and compositions that are effective in the prevention and treatment of viral diseases, particularly diseases caused by hantavirus species.

[0008] In this regard, ongoing research into the usefulness of MEK inhibitors in the treatment of other viral diseases, especially influenza, has revealed that this class of compounds avoids the drawbacks of standard antiviral treatments because they are directed at cellular components of host cells rather than the virus itself. For this reason, resistance to MEK inhibitors has not been observed. WO2001 / 076570 provides a concept for treating or preventing infections caused by negative RNA viruses (especially influenza viruses) with MEK inhibitors. WO2014 / 056894 provides specific MEK inhibitors, such as AZD-6244, AZD-8330, RDEA-119, GSK-1120212 (trametinib), GDC-0973 (cobimetinib), CI-1040, PD-0325901, RO-5126766, and MSC1936369 (AS-703026), for use in the treatment or prevention of influenza virus infections. WO2015 / 173788A1 discloses MEK inhibitors for use in methods for treating influenza virus and bacterial co-infection. In addition, WO2019 / 076947 discloses a new MEK inhibitor, PD-0184264 (also known as ATR-002), for use in methods for preventing and / or treating influenza virus infection.

[0009] However, none of these documents indicate that MEK inhibitors can be used for hantavirus infections, and there remains a strong need to provide compositions and compounds for the treatment and prevention of hantavirus infections. Summary of the Invention

[0010] In the present invention, the use of MEK inhibitors in the treatment or prevention of hantavirus infection has been shown to provide effective treatment for viral infections. Specifically, administration of the MEK inhibitors CI-1040 or PD-0184264 to mice infected with hantavirus resulted in a significant reduction in viral load.

[0011] Thus, the present invention relates to MEK inhibitors for use in the treatment or prevention of hantavirus infection in mammals, preferably humans or rodents.

[0012] In the context of the present invention, the MEK inhibitor may be selected from the group consisting of CI-1040, PD-0184264, GSK-1120212, GDC-0973, PLX-4032, AZD6244, AZD8330, AS-703026, RDEA-119, RO-5126766, RO-4987655, PD-0325901, TAK-733, AS703026, PD98059, and PD184352, or a pharmaceutically acceptable salt or metabolite thereof. In a preferred aspect, the MEK inhibitor is CI-1040 or PD-0184264.

[0013] In human patients, MEK inhibitors can be administered to treat hantavirus infections when the patient exhibits symptoms of hantavirus hemorrhagic fever with renal syndrome (HFRS) or hantavirus pulmonary syndrome (HPS). In these cases, MEK inhibitors can be administered up to 12 hours, 24 hours, 48 ​​hours, 72 hours, or 4 to 10 days after the first symptoms of HFRS or HPS are observed.

[0014] MEK inhibitors can also be administered to human subjects who have come into contact with rodents or rodent excreta or who are in areas where hantavirus epidemics are common, for the prevention of hantavirus infection.

[0015] Administration of a MEK inhibitor for the treatment or prevention of hantavirus infection is particularly indicated when a human subject resides in or has been present in an area known to have hantavirus infections that cause HFRS or HPS.

[0016] Such hantavirus infections can be hantavirus infections or dobravavirus infections, or hantavirus infections caused by American species such as Black Creek Canal virus (BCCV), New York orthohantavirus (NYV), Monongahela virus (MGLV), Sin Nombre orthohantavirus (SNV), or Andes virus.

[0017] MEK inhibitors for use in the present invention may preferably be administered orally or by inhalation.

[0018] In a further aspect, the treatment of rodent populations with MEK inhibitors is contemplated to prevent infection in humans who come into contact with the rodents. In such uses, the MEK inhibitors can be administered by inhalation, for example, via environmental spraying. [The present invention 1001] A MEK inhibitor for use in the treatment or prevention of hantavirus infection in a mammal. [The present invention 1002] The MEK inhibitor for use in the present invention 1001 is selected from the group consisting of CI-1040, PD-0184264 GSK-1120212, GDC-0973, PLX-4032, AZD6244, AZD8330, AS-703026, RDEA-119, RO-5126766, RO-4987655, PD-0325901, TAK-733, AS703026, PD98059, and PD184352, or a pharmaceutically acceptable salt or metabolite thereof. [The present invention 1003] The MEK inhibitor for use in the present invention 1002, which is CI-1040 or PD-0184264. [The present invention 1004] The MEK inhibitor for use in any of claims 1001 to 1003, wherein the mammal is a rodent or a human. [The present invention 1005] The MEK inhibitor for use in accordance with the present invention 1004, wherein the mammal is a human, and the human exhibits symptoms of Hantavirus hemorrhagic fever with renal syndrome (HFRS) or Hantavirus pulmonary syndrome (HPS). [The present invention 1006] The MEK inhibitor for use in the present invention 1005, wherein the MEK inhibitor is administered within 12 hours, 24 hours, 48 ​​hours, 72 hours, or 4 to 10 days after the first symptoms of HFRS or HPS are observed. [The present invention 1007] A MEK inhibitor for use in any of the present inventions 1001 to 1006, administered to a human subject who has come into contact with a rodent or rodent excrement or who is in an area where hantavirus epidemics are common, for the prevention of hantavirus infection. [The present invention 1008] A MEK inhibitor for use in any of claims 1004 to 1007, wherein the human subject resides in or has been staying in an area known to have hantavirus infections that cause HFRS or HPS. [The present invention 1009] The MEK inhibitor for use in the present invention 1008, wherein the hantavirus is a hantavirus infection or a Dobrava virus infection, or a hantavirus infection caused by an American species such as Black Creek Canal virus (BCCV), New York Orthohantavirus (NYV), Monongahela virus (MGLV), Sin Nombre Orthohantavirus (SNV), or Andes virus. [The present invention 1010] A MEK inhibitor for use in any of the present inventions 1001 to 1009, administered orally or by inhalation. [The present invention 1011] 1004. The MEK inhibitor for use in accordance with the present invention, wherein the mammal is a rodent and the MEK inhibitor is administered to a population of rodents to prevent infection in humans who come into contact with the rodents. [The present invention 1012] The MEK inhibitor for use in the present invention 1011, administered by inhalation. [Brief explanation of the drawings]

[0019] [Figure 1] We show that in the presence of CI-1040, a significant viral titer reduction of >2 log10 steps was achieved compared to the solvent control, which equates to a viral titer reduction of >99%. [Figure 2] Figure 1 shows that in the presence of ATR-002, a >1.5 log10 step reduction in viral titer was achieved compared to the solvent control, which equates to a >90% reduction in viral titer. [Figure 3] 1 shows that no virus was detectable in the lungs of animals treated with 75 mg / kg / day ATR-002 at days 7 and 10 post-infection. [Figure 4] 1 shows that virus could not be detected in the kidneys of animals treated with 75 mg / kg / day of ATR-002 at days 7 and 10 post-infection. DETAILED DESCRIPTION OF THE INVENTION

[0020] Detailed Description The following description contains information that may be useful in understanding the present invention. None of the information provided herein is admitted to be prior art or relevant to the claimed invention, nor is any publication specifically or implicitly referenced admitted to be prior art.

[0021] As used herein, "MEK inhibitor" refers to inhibiting the mitogenic signaling cascade Raf / MEK / ERK in cells or in a subject by inhibiting MEK (mitogen-activated protein kinase kinase). This signaling cascade is hijacked by many viruses, especially influenza viruses, to promote viral replication. Therefore, specific blocking of the Raf / MEK / ERK pathway at the bottleneck MEK attenuates the proliferation of viruses, especially influenza viruses. Furthermore, MEK inhibitors have low toxicity and show few adverse side effects in humans. They also tend not to induce viral resistance (Ludwig, 2009). A particularly preferred MEK inhibitor is PD-0184264, also known as ATR-002.

[0022] The MEK inhibitor is preferably selected from CI-1040, PD-0184264 GSK-1120212, GDC-0973, PLX-4032, AZD6244, AZD8330, AS-703026, RDEA-119, RO-5126766, RO-4987655, PD-0325901, TAK-733, AS703026, PD98059, and PD184352, or pharmaceutically acceptable salts or metabolites thereof. These MEK inhibitors are known in the art and are listed, for example, in Table 1 of Fremin and Meloche (2010), J. Hematol. Oncol. 11;3:8. The structural formulas of PD-0184264 and CI-1040 are provided below for reference. TIFF0007802365000001.tif46128TIFF0007802365000002.tif65128

[0023] "Metabolite," as used herein, refers to an intermediate end product of the metabolism of a MEK inhibitor that occurs during the degradation of the MEK inhibitor by a subject, for example, in the liver. In a preferred embodiment, the MEK inhibitor is a metabolite of CI-1040, for example, PD-0184264 is a metabolite of the MEK inhibitor CI-1040.

[0024] For the purposes of the present invention, the MEK inhibitor defined above also includes its pharmaceutically acceptable salt.As used herein, the phrase "pharmaceutically or cosmetically acceptable salt" refers to a salt of the compound of the present invention that is safe and effective for the desired administration form.Pharmaceutically acceptable salts include those formed with anions such as those derived from hydrochloric acid, phosphoric acid, acetic acid, oxalic acid, tartaric acid, etc., and those formed with cations such as those derived from sodium hydroxide, potassium hydroxide, ammonium hydroxide, calcium hydroxide, ferric hydroxide, isopropylamine, triethylamine, 2-ethylaminoethanol, histidine, procaine, etc.

[0025] As outlined above, hantavirus infections are a global public health concern. Currently, there are no WHO- or FDA-approved vaccines or antiviral drugs targeting hantaviruses. However, in the context of influenza treatment, we have previously demonstrated the antiviral potential of MEK inhibitors, such as CI-140 and PD0184264 (ATR002) (the active metabolite of CI-1040), against influenza viruses at in vitro and in vivo levels. The results presented below demonstrate that hantavirus growth was successfully reduced in Vero cells treated with 40 μM CI-1040 or 40 μM ATR-002 in in vitro experiments. In Example 1, a >90% reduction in virus titer was observed compared to the solvent control; see Figures 1 and 2. Furthermore, as described in Example 2 and Figures 3 and 4, in vivo experiments demonstrated that treatment of mice with 75 mg / Kg / day of ATR-002 for 5 days resulted in complete viral titer reduction compared to animals treated with vehicle alone.

[0026] Although hantaviruses replicate in the cytoplasm and are not known to have a nuclear phase, PUUV growth was successfully impaired by inhibiting the Raf / MEK / ERK pathway with the MEK inhibitors ATR-002 or CI-1040.

[0027] Viral infections that may be prevented or treated by administration of the MEK inhibitors of the present invention are infections caused by hantaviruses. Known hantaviruses include Puumala virus, Sin Nombre virus, Seoul virus, Hantaan virus, Dobrava-Belgredo virus, Saaremaa virus, and Andes virus.

[0028] As already mentioned above, hantavirus infection manifests in two clinical manifestations: the first, Hantavirus Hemorrhagic Fever with Renal Syndrome (HFRS), with a mortality rate of 12%, and the second, Hantavirus Pulmonary Syndrome (HPS), with a mortality rate of 40%. The severity of the disease depends on the causative hantavirus species and viral load. For example, severe disease courses are known to be caused by Hantavirus, Dobrava-Belgredo virus, Sin Nombre virus, and Andes virus, while more moderate disease courses are more likely in, for example, Puumala virus or Saaremaa virus.

[0029] Hantavirus hemorrhagic fever with renal syndrome (HFRS) is also known as Korean hemorrhagic fever, epidemic hemorrhagic fever, and epidemic nephropathy. Species that cause HFRS include Hantaan orthohantavirus, Dobrava-Belgrade orthohantavirus, Saaremaa virus, Seoul orthohantavirus, Puumala orthohantavirus, and other Eurasian orthohantaviruses. HFRS symptoms usually appear within 1–2 weeks after exposure to infectious agents, but in rare cases, they may take up to 8 weeks to develop. Early symptoms begin suddenly and include severe headache, back and abdominal pain, fever, chills, nausea, and blurred vision. Individuals may have facial flushing, eye inflammation or redness, or a rash. Late symptoms may include hypotension, acute shock, vascular leakage, and acute renal failure, which can lead to severe fluid overload.

[0030] The severity of the disease varies depending on the virus causing the infection: Hantan and Dobrava virus infections usually cause severe symptoms, while Seoul, Saaremaa, and Puumala virus infections are usually more moderate.

[0031] The syndrome can also be fatal. In some cases, it is known to cause permanent renal failure. HFRS is difficult to diagnose on clinical grounds alone; serological evidence is often required. A four-fold rise in IgG antibody titers within a one-week interval and the presence of IgM antibodies to hantavirus are sufficient evidence of acute hantavirus infection. HFRS should be suspected in patients with acute febrile influenza-like illness, unexplained renal failure, and occasionally liver dysfunction.

[0032] Hantavirus pulmonary syndrome (HPS) is generally caused by American species of hantaviruses. These include Black Creek Canal virus (BCCV), New York orthohantavirus (NYV), Monongahela virus (MGLV), Sin Nombre orthohantavirus (SNV), and certain other members of the Hantavirus genus native to the United States and Canada. Certain rodents are the primary hosts of hantaviruses, including the allied cotton rat (Sigmodon hispidus) in South Florida, the primary host of Black Creek Canal virus; the deer mouse (Peromyscus maniculatus) in Canada and the western United States, the primary host of Sin Nombre virus; and the white-footed mouse (Peromyscus leucopus) in the eastern United States, the primary host of New York virus. In South America, Oligoryzomys longicaudatus and other species of the genus Oligoryzomys have been recorded as reservoirs for Andes viruses.

[0033] Symptoms of HPS include flu-like symptoms, such as fever, cough, muscle aches, headache, lethargy, and shortness of breath, which rapidly worsen to acute respiratory failure. It is characterized by the sudden onset of shortness of breath accompanied by rapid progression of pulmonary edema; it is often fatal despite intervention with mechanical ventilation and potent diuretics. It has a 36% case-fatality rate. HPS is often overlooked because its initial symptoms mimic those of influenza. Infected patients suffer from fatigue, fever, and muscle aches, often accompanied by headache, dizziness, and gastrointestinal problems, for several weeks after exposure. Approximately one week after the initial symptoms subside, the second stage of the disease begins, and patients experience severe coughing and shortness of breath as fluid accumulates in the lungs. In the later stages of HPS, the lungs are severely damaged, resulting in a high case-fatality rate.

[0034] In the treatment or prophylaxis use of the present invention, the patient is preferably a mammal, in a preferred embodiment a primate, and most preferably a human patient. In an alternative administration, treatment of mammals known to be carriers of hantavirus, such as rodents and bats, particularly rats, mice, and deer mice, is contemplated to prevent human infection via these hosts. In this context, widespread administration via inhalation (environmental spray formulation) may be considered in places with high hantavirus infection rates. Because human-to-human transmission is rare in hantavirus infections, such widespread application to mammalian non-human hosts, such as rodents, may act as a preventative measure.

[0035] Additionally, administration of MEK inhibitors to human subjects who have come into contact with rodents or rodent excreta or who reside or travel in areas where hantavirus outbreaks are common, for the prevention of hantavirus infection, may be useful, particularly if the human subject resides or is staying in an area known to have hantavirus infections that cause HFRS or HPS.

[0036] Specifically, such prophylaxis or preventative treatment would be effective if a human patient has traveled to or resided in areas of South Korea, Serbia, or the United States where hantavirus infection or Dobrava virus infection, or hantavirus infection caused by American species such as Black Creek Canal virus (BCCV), New York Orthohantavirus (NYV), Monongahela virus (MGLV), Sin Nombre Orthohantavirus (SNV), or Andes virus, is known. Because transmission of hantavirus species occurs primarily through aerosolized rodent excreta (urine, saliva, feces), prophylaxis can be initiated immediately after contact with rodent excreta, up to 10 days after contact, without symptoms of infection.

[0037] The MEK inhibitor may be administered orally, intravenously, intrathoracically, intramuscularly, topically, or by inhalation. Preferably, the MEK inhibitor is administered by inhalation or orally.

[0038] Additionally, MEK inhibitors can be administered up to 12 hours, 24 hours, 48 ​​hours, 72 hours, or 4-10 days after the first symptoms of HFRS or HPS are observed or after the human patient comes into contact with rodent excreta.

[0039] In one embodiment of the present invention for use in treatment or prevention, the compound MEK inhibitor can be administered orally or by inhalation in an effective therapeutic dosage. In one embodiment, the therapeutically effective amount of the MEK inhibitor is, for example, 0.1 mg to 2000 mg, 0.1 mg to 1000 mg, 0.1 to 500 mg, 0.1 to 200 mg, 30 to 300 mg, 0.1 to 75 mg, or 0.1 to 30 mg.

[0040] As outlined above, the present invention further provides a pharmaceutical composition comprising a MEK inhibitor, or a pharmaceutically acceptable salt or metabolite thereof, for use as a medicament for the prevention and / or treatment of a viral infection, preferably an infection caused by a hantavirus.

[0041] The pharmaceutical compositions of the present invention can be in the form of orally administrable suspensions or tablets, nasal sprays, sterile injectable preparations (intravenous, intrathoracic, intramuscular), such as sterile injectable aqueous or oily suspensions, or suppositories.When administered orally as suspensions, these compositions can be prepared according to the techniques available in the pharmaceutical formulation art, and can contain microcrystalline cellulose as a bulking agent, alginic acid or sodium alginate as a suspending agent, methylcellulose as a thickening agent, and sweeteners / flavorings known in the art.As immediate-release tablets, these compositions can contain microcrystalline cellulose, dicalcium phosphate, starch, magnesium stearate, and lactose, and / or other excipients, binders, fillers, disintegrants, diluents, and lubricants known in the art. Injectable solutions or suspensions can be formulated according to the known art using suitable non-toxic parenterally acceptable diluents or solvents, such as mannitol, 1,3-butanediol, water, Ringer's solution, or isotonic sodium chloride solution, or suitable dispersing or wetting agents and suspending agents, such as sterile, bland fixed oils, including synthetic mono- or diglycerides, and fatty acids, including oleic acid. The pharmaceutical compounds in the methods of the present invention can be administered in any suitable unit dosage form. Suitable oral formulations, even in the context of the pharmaceutical compositions of the present invention, can be tablets, capsules, suspensions, syrups, chewing gum, wafers, elixirs, and other dosage forms. Pharmaceutically acceptable carriers, such as binders, excipients, lubricants, and sweeteners or flavoring agents, can be included in oral pharmaceutical compositions. Conventional substances can also be included to modify the taste, color, and shape of particular dosage forms, if desired.

[0042] For injectable formulations, the pharmaceutical composition may be a lyophilized powder mixed with a suitable excipient in a suitable vial or tube. Prior to use in the clinic, the drug may be reconstituted by dissolving the lyophilized powder in a suitable solvent system to form a composition suitable for intravenous or intramuscular injection.

[0043] In one embodiment, the pharmaceutical composition can be in an orally administrable dosage form (e.g., a tablet, capsule, or syrup, etc.) having a therapeutically effective amount (e.g., 0.1 mg to 2000 mg, 0.1 mg to 1000 mg, 0.1 to 500 mg, 0.1 to 200 mg, 30 to 300 mg, 0.1 to 75 mg, 0.1 to 30 mg) of a MEK inhibitor.

[0044] definition Throughout this specification and the claims that follow, unless the context requires otherwise, the word "comprise" and variations thereof, such as "comprises" and "comprising," are understood to imply the inclusion of a stated integer or step or group of integers or steps, but not the exclusion of any other integer or step or group of integers or steps. As used herein, the term "comprising" can be replaced with the term "containing," or in some cases, when used herein, with the term "having."

[0045] As used herein, "consisting of" excludes any element, step, or ingredient not specified in the claim element. As used herein, "consisting essentially of" does not exclude materials or steps that do not materially affect the basic and novel characteristics of the claim. In each instance herein, any of the terms "comprising," "essentially consisting of," and "consisting of" may be replaced with either of the other two terms.

[0046] As used herein, the conjunction "and / or" between multiple listed elements is understood to encompass both individual and compound element alternatives. For example, when two elements are connected by "and / or," the first alternative means that the first element is applicable without the second element. The second alternative means that the second element is applicable without the first element. The third alternative means that both the first and second elements are applicable. Any of these alternatives are understood to be within the meaning of, and therefore satisfy the requirements of, the term "and / or" as used herein. The simultaneous applicability of multiple alternatives is also understood to be within the meaning of, and therefore satisfy the requirements of, the term "and / or" as used herein. [Example]

[0047] material: Puumala virus (PUUV) strain Sotkamo - Major hantavirus species in Europe - Can be handled in the S2 laboratory Vero cell line - African green monkey kidney cell line - routinely used to grow viruses - Type I interferon deficiency Cell culture medium: · Basic medium: IMDM, 1% P / S, 1% L-Gln, 10% FCS ATR-002 / CI-1040 treatment medium: basal medium without FCS Viral infection medium: basal medium without FCS

[0048] The MEK inhibitor ATR-002 (PD0184264) [2-(2-chloro-4-iodophenylamino)-N-3,4-difluorobenzoic acid (the active metabolite of CI-1040)] was synthesized at ChemCon GmbH (Freiburg, Germany).

[0049] The MEK inhibitor CI-1040 [2-(2-chloro-4-iodophenylamino)-N-(cyclopropylmethoxy)-3,4-difluorobenzamide] was synthesized at ChemCon GmbH (Freiburg, Germany).

[0050] Example 1: Viral yield reduction assay method: Vero cells were cultured in a 24-well plate (1x10 6 The cells were seeded in 1000 μl of ...

[0051] One day after seeding, the cells were infected with PUU viral particles (MOI 0.3).

[0052] At 1 h postinfection, cells were treated with 40 μM CI-1040, 40 μM ATR-002, or DMSO (solvent control).

[0053] Supernatants were collected 72 hours post-infection, and virus titers were determined using the following TCID 50 Determined by assay.

[0054] TCID 50 Assay (SOP-ATR-0119) Virus titration was performed using standard operating procedure SOP-ATR-0119. Briefly, 10% homogenates from lung and kidney / supernatant from the VYR assay were diluted in 1:10 serial dilutions. Vero cells were infected with various 10-fold virus dilutions and incubated for 60 minutes at 37°C in a 5% CO2 atmosphere. After incubation, cells were rinsed with PBS and supplemented with 200 μl IMDM (Iscove's Modified Dulbecco's Medium) / BA (bovine albumin)-medium (0.2% BA, 1 mM MgCl2, 0.9 mM CaCl2, 100 U / ml penicillin, 0.1 mg / ml streptomycin) and incubated for 7 days at 37°C in a 5% CO2 atmosphere. Vero cells were then washed and fixed with Roti®-Histofix for 30 minutes at 4°C. After washing with PBS, cells were permeabilized with Triton-X-100 and FCS. The primary antibody (anti-PUUV-NP-AB) incubation was maintained for 1 hour. After washing, the secondary antibody was applied to the cells for 30 minutes. The cells were then washed and stained with the substrate TrueBlue for 10 minutes. Analysis was performed by light microscopy.

[0055] result: As can be seen from Figure 1, in the presence of CI-1040, >2 log 10 A significant stepwise reduction in virus titer was achieved compared to the solvent control, equivalent to a >99% reduction in virus titer.

[0056] In the presence of ATR-002, similar results are seen in Figure 2, with a >1.5 log 10 A stepwise viral titer reduction was achieved compared to the solvent control, which equates to a viral titer reduction of >90%.

[0057] Conclusion: Treatment of Vero cells infected with PUUV (MOI 0.3) with either 40 μM CI-1040 or 40 μM ATR-002 results in a strong reduction in virus titer compared to the solvent control.

[0058] Inhibition of the Raf / MEK / ERK pathway attenuated Puumala virus growth in vitro.

[0059] Example 2: Antiviral Effect of ATR-002 against Hantavirus in Vivo material and method mouse A robust, established animal model for studying hantavirus infection was not available. Type I interferon-deficient Vero cells proved to be a good in vitro model, but type I interferon-deficient mice were not available. Therefore, interferon receptor knockout mice (IFNα / β / γR- / - (AG129) mice) were selected for in vivo studies. AG129 mice were used in the following experiments.

[0060] method AG129 mice were infected intranasally with PUUV (5x10 in 50 μl PBS). 5 / pfu, 25 μl inoculated into each nostril).

[0061] Treatment with ATR-002 (in DMSO / Cremophor EL / PBS) at 75 mg / Kg / day for 5 consecutive days starting 5 hours after infection. Route of administration: oral gavage, 37.5 mg / kg twice daily (9 AM and 6 PM). Control group treated accordingly with vehicle only.

[0062] To determine the viral titer in the lungs and kidneys (TCID 50 assay), mice were sacrificed on days 7 and 10 postinfection.

[0063] result Following PUUV infection, none of the animals lost weight, developed clinical signs, or died.

[0064] PUUV was detectable in the lungs and kidneys of vehicle control animals on days 7 and 10 post-infection. Viral titers were higher on day 10.

[0065] As seen in Figures 3 and 4, respectively, virus was undetectable in the lungs and kidneys of animals treated with 75 mg / kg / day of ATR-002 on days 7 and 10 post-infection (detection limits: lung: 3.4 log 10 (TCID 50 / g organ) Kidney: 3.2 log 10 (TCID 50 / g organs).

[0066] The reduction in viral load (comparing homogenates treated with solvent control to homogenates treated with ATR-002) was highly significant (two-way ANOVA, P<0.0001).

[0067] conclusion This study demonstrated that treatment of mice with 75 mg / Kg / day of ATR-002 (in DMSO / Cremophor EL / PBS) for 5 days, starting 5 hours after PUUV infection, significantly reduced the viral load in the lungs and kidneys.

Claims

1. 1. A pharmaceutical composition comprising a MEK inhibitor for use in treating or preventing hantavirus infection in a mammal, wherein the MEK inhibitor is CI-1040 or PD-0184264, or a pharmaceutically acceptable salt thereof.

2. 10. The pharmaceutical composition of claim 1, wherein the mammal is a rodent or a human.

3. 3. The pharmaceutical composition of claim 2, wherein the mammal is a human and the human exhibits symptoms of Hantavirus hemorrhagic fever with renal syndrome (HFRS) or Hantavirus pulmonary syndrome (HPS).

4. 4. The pharmaceutical composition of claim 3, wherein the composition is administered within 12 hours, within 24 hours, within 48 hours, within 72 hours, or between 4 and 10 days after the first symptoms of HFRS or HPS are observed.

5. 5. The pharmaceutical composition of any one of claims 1 to 4, wherein the composition is administered to a human subject who has come into contact with a rodent or rodent excreta or who is in an area where endemic hantavirus infections are common, for the prevention of hantavirus infections.

6. 6. The pharmaceutical composition of any one of claims 2-5, wherein the human subject resides in or has been staying in an area known to have hantavirus infections that cause HFRS or HPS.

7. 7. The pharmaceutical composition of claim 6, wherein the hantavirus infection is a hantavirus infection or a Dobrava virus infection, or a hantavirus infection caused by an American species such as Black Creek Canal virus (BCCV), New York Orthohantavirus (NYV), Monongahela virus (MGLV), Sin Nombre Orthohantavirus (SNV), or Andes virus.

8. 8. The pharmaceutical composition of any one of claims 1 to 7, which is administered orally or by inhalation.

9. 3. The pharmaceutical composition of claim 2, wherein the mammal is a rodent and the composition is administered to a rodent population to prevent infection in humans who come into contact with the rodents.

10. 10. The pharmaceutical composition of claim 9, wherein the composition is administered by inhalation.

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