PHARMACEUTICAL COMBINATION COMPRISING A BRAIN AMINOPEPTIDASE A INHIBITOR, A DIURETIC AND A BLOCKER OF THE SYSTEMIC RENIN-ANGIOTENSIN SYSTEM

Abstract

The present invention relates to a pharmaceutical combination comprising (i) firibastat, (ii) a diuretic and (iii) a blocker of the systemic renin-angiotensin system selected from the group consisting of angiotensin I converting enzyme inhibitors (ACEIs) and angiotensin II receptor type 1 (AT1R) antagonists. Said composition is particularly useful for the treatment of hypertension and related diseases and conditions.

Claims

1-21. (canceled)

22. A method of treating arterial hypertension or indirectly or heart failure comprising administering a pharmaceutical combination comprising (i) firibastat, (ii) a diuretic and (iii) a blocker of the systemic renin-angiotensin system selected from the group consisting of angiotensin I converting enzyme inhibitors and angiotensin II receptor type 1 antagonists to a subject in need of treatment.

23. The method according to claim 22, wherein the diuretic is selected from the group consisting of chlorothiazide, hydrochlorothiazide, chlorthalidone, indapamide, furosemide, torsemide, amiloride, triamterene, spironolactone and eplerenone.

24. The method according to claim 23, wherein the diuretic is hydrochorothiazide.

25. The method according to claim 22, wherein the blocker of the systemic renin-angiotensin system is selected from the group of angiotensin converting enzyme inhibitors consisting of lisinopril, enalapril, quinapril, ramipril, benazepril, captopril, cilazapril, fosinopril, imidapril, moexipril, trandolapril, or perindopril.

26. The method according to claim 22, wherein the blocker of the systemic renin-angiotensin system is enalapril.

27. The method according to claim 22, wherein the blocker of the systemic renin-angiotensin system is selected from the group consisting of angiotensin II receptor type 1 antagonists consisting of losartan, candesartan, irbesartan, telmisartan, valsartan, olmesartan, eprosartan and azilsartan.

28. The method according to claim 22, wherein the blocker of the systemic renin-angiotensin system is valsartan.

29. The method according to claim 22, wherein the diuretic is hydrochlorothiazide and the blocker of the systemic renin-angiotensin system is enalapril.

30. The method according to claim 22, wherein the diuretic is hydrochlorothiazide and the blocker of the systemic renin-angiotensin system is valsartan.

31. The method according to claim 22, wherein the diuretic is indapamide and the blocker of the systemic renin-angiotensin system is perindopril.

32. The method according to claim 22, wherein the diuretic is chlorthalidone and the blocker of the systemic renin-angiotensin system is azilsartan.

33. The method according to claim 29, containing firibastat in an amount in the range from 100 to 1500 mg, hydrochlorothiazide in an amount in the range from 5 to 30 mg, and enalapril in an amount in the range from 2.5 to 50 mg.

34. The method according to claim 29, containing firibastat in an amount in the range from 300 to 600 mg, hydrochlorothiazide in an amount in the range from 5 to 15 mg, and enalapril in an amount in the range from 2.5 to 15 mg.

35. The method according to claim 22, wherein the three active ingredients are administered simultaneously or sequentially.

36. A kit of parts comprising a pharmaceutical combination containing (i) firibastat, (ii) a diuretic, (iii) a blocker of the systemic renin-angiotensin system selected from the group consisting of angiotensin I converting enzyme inhibitors and angiotensin II receptor type 1 antagonists, in the form of one, two or three separate units of the components (i) to (iii), for a simultaneous or sequential administration.

37. The kit according to claim 36, wherein (ii) the diuretic is selected from the group consisting of hydrochorothiazide, indapamide, amiloride and chlorthalidone, and (iii) the blocker of the systemic renin-angiotensin system is selected from the group consisting of angiotensin I converting enzyme inhibitors consisting of enalapril, perindopril, ramipril and benazepril or from angiotensin II receptor type 1 antagonists the group consisting of losartan, valsartan, candesartan, irbesartan and azilsartan.

38. The kit according to claim 36, wherein (ii) the diuretic is hydrochlorothiazide and (iii) the blocker of the systemic renin-angiotensin system is enalapril.

39. The kit according to claim 36, wherein (ii) the diuretic is hydrochlorothiazide and (iii) the blocker of the systemic renin-angiotensin system is valsartan.

40. The kit according to claim 36, wherein (ii) the diuretic is indapamide and (iii) the blocker of the systemic renin-angiotensin system is perindopril.

41. The kit according to claim 36, wherein (ii) the diuretic is chlorthalidone and (iii) the blocker of the systemic renin-angiotensin system is azilsartan.

Description

DESCRIPTION OF THE FIGURES

[0018] FIG. 1. (A) Effects of enalapril, HCTZ or firibastat, given orally alone or in combination on mean arterial blood pressure (MABP) in conscious DOCA-salt rats.

[0019] MABP values (mmHg, mean±SEM) at baseline or 5 hours after a single oral administration of saline, enalapril (10 mg/kg), HCTZ (10 mg/kg), firibastat (30 mg/kg), firibastat (30 mg/kg) plus enalapril (10 mg/kg), firibastat (30 mg/kg) plus HCTZ (10 mg/kg), enalapril (5 mg/kg) plus HCTZ (5 mg/kg), firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) in conscious DOCA-salt rats. (n=6 for each treatment). One-way ANOVA followed by Sidak's multiple comparisons test, ns: non-significant, * P<0.05; ** P<0.01; *** P<0.0001, when compared to corresponding baseline MABP values.

[0020] FIG. 1. (B) Changes from baseline after 5 hours post-dosing in mean arterial blood pressure (MABP) after a single oral administration of enalapril, HCTZ or firibastat given alone or in combination in conscious DOCA-salt rats.

[0021] Mean±SEM changes in MABP (mmHg) from baseline after 5 hours following a single oral administration of saline, enalapril (10 mg/kg), HCTZ (10 mg/kg), firibastat (30 mg/kg), firibastat (30 mg/kg) plus enalapril (10 mg/kg), firibastat (30 mg/kg) plus HCTZ (10 mg/kg), enalapril (5 mg/kg) plus HCTZ (5 mg/kg), firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) in conscious DOCA-salt rats (n=6 per group). One-way ANOVA followed by Sidak's multiple comparisons when compared to changes in MABP values obtained in DOCA-salt rats receiving saline, * P<0.01; ** P<0.001; *** P<0.0001 or Tukey's multiple comparisons test when compared to changes MABP values obtained in DOCA-salt receiving firibastat plus enalapril plus HCTZ, #P<0.05; ##P<0.01; ###P<0.0001.

[0022] FIG. 2. Effects of enalapril, HCTZ or firibastat, given orally alone or in combination on heart rate (HR) in conscious DOCA-salt rats.

[0023] HR values (bpm, mean±SEM) at baseline or 5 hours after a single oral administration of saline, enalapril (10 mg/kg), HCTZ (10 mg/kg), firibastat (30 mg/kg), firibastat (30 mg/kg) plus enalapril (10 mg/kg), firibastat (30 mg/kg) plus HCTZ (10 mg/kg), enalapril (5 mg/kg) plus HCTZ (5 mg/kg), firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) in conscious DOCA-salt rats. (n=6 for each treatment). One-way ANOVA followed by Sidak's multiple comparisons test, ns: non-significant, when compared to corresponding baseline HR values.

[0024] FIG. 3. (A) Time course of mean arterial blood pressure (MABP) after chronic oral administration of enalapril, HCTZ or firibastat, given orally in combination in conscious DOCA-salt rats.

[0025] MABP values (mmHg, mean±SEM) on day 8 at baseline, 5, 9 or 24 hours after a daily chronic oral administration of saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) over 8 consecutive days in conscious DOCA-salt rats. (n=12 for each treatment). One-way ANOVA followed by Holm-Sidak's multiple comparisons test, * P<0.05; ** P<0.01; *** P<0.0001, when compared to the corresponding studied time MABP values obtained in DOCA-salt rats receiving saline.

[0026] FIG. 3. (B) Time course of mean arterial blood pressure (MABP) changes from baseline after a daily chronic oral administration of enalapril, HCTZ or firibastat given in combination during 8 days in conscious DOCA-salt rats. Mean±SEM changes in MABP (mmHg) from baseline to day 8 after 5, 9 or 24 hours following a daily chronic oral administration of saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) during 8 consecutive days in conscious DOCA-salt rats. (n=12 for each treatment). One-way ANOVA followed by Holm-Sidak's multiple comparisons test, * P<0.05; ** P<0.001; *** P<0.0001 when compared to changes in MABP values obtained in DOCA-salt rats receiving saline or Sidak's multiple comparisons test, #P<0.05, when compared to changes in MABP values obtained in DOCA-salt receiving firibastat plus enalapril plus HCTZ.

[0027] FIG. 4. Time course of heart rate (HR) after chronic oral administration of enalapril, HCTZ or firibastat, given in combination in conscious DOCA-salt rats.

[0028] HR values (bpm, mean±SEM) 5, 9 or 24 hours after a daily chronic oral administration of saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) during 8 days in conscious DOCA-salt rats. (n=12 for each treatment). One-way ANOVA followed by Tukey's multiple comparisons test, ns: non-significant, when compared to DOCA-salt rats receiving saline or enalapril plus HCTZ.

[0029] FIG. 5. Effects of chronic oral RB150 treatment on plasma arginine vasopressin (AVP) release in conscious hypertensive DOCA-salt rats.

[0030] Plasma AVP levels were assessed by radioimmunoassay after daily 10-day chronic oral administration of saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) in conscious DOCA-salt rats. The results were expressed as picogram of AVP per milliliter of plasma. Values are expressed as mean±SEM of 10 animals individually analyzed for each condition. One-way ANOVA followed by Tukey's test, ns: non-significant, * P<0.05; ** P<0.001 when compared to the corresponding plasma AVP values obtained in DOCA-salt rats receiving saline or enalapril plus HCTZ.

SUMMARY OF THE INVENTION

[0031] In one embodiment, the present invention relates to a pharmaceutical combination comprising (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs.

[0032] Said combination is particularly useful for the treatment of arterial HTN or indirectly or directly related diseases.

[0033] In accordance with another embodiment of the present invention, a method is disclosed for the treatment of HTN and indirectly or directly related diseases. The method and use of the invention comprises administering to a subject in need of such treatment an effective amount of a pharmaceutical composition comprising (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs, or, where appropriate, for each active ingredient (i)-(iii) a pharmaceutically acceptable salt or solvate thereof.

[0034] In yet another embodiment, the invention relates to a kit of parts comprising a pharmaceutical combination as defined above, for a simultaneous or sequential administration, preferably for simultaneous administration.

DESCRIPTION OF THE INVENTION

[0035] The present invention relates to a pharmaceutical combination, comprising (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs, more particularly for use in the treatment of arterial HTN or indirectly or directly related diseases.

[0036] The invention likewise relates to the use of (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs, for the manufacture of a medicament for the treatment of arterial HTN or indirectly or directly related diseases.

[0037] The invention likewise relates to a method for the treatment of arterial HTN or indirectly or directly related diseases, comprising administering to a patient, including human and non-human subjects, a therapeutically effective amount of (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs.

[0038] The invention furthermore relates to a kit of parts comprising (i) firibastat or a pharmaceutically acceptable salt or solvate thereof, (ii) a diuretic or a pharmaceutically acceptable salt or solvate thereof, (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs, or a pharmaceutically acceptable salt or solvate thereof, for a simultaneous or sequential administration of said three active ingredients (i)-(iii), more preferably in the form of one or more separate dosage units of the active ingredients (i) to (iii) or pharmaceutical compositions comprising the active ingredients (i) to (iii).

[0039] According to the invention, the term “comprise(s)” or “comprising” (and other comparable terms, e.g., “containing,” and “including”) is “open-ended” and can be generally interpreted such that all of the specifically mentioned features and any optional, additional and unspecified features are included. According to specific embodiments, it can also be interpreted as the phrase “consisting essentially of” where the specified features and any optional, additional and unspecified features that do not materially affect the basic and novel characteristic(s) of the claimed invention are included or the phrase “consisting of” where only the specified features are included, unless otherwise stated.

[0040] According to the invention, the diuretics include more particularly chlorothiazide, hydrochlorothiazide, chlorthalidone, indapamide, furosemide, torsemide, amiloride, triamterene, spironolactone and eplerenone. According to a preferred embodiment, the diuretic is selected from the group consisting of hydrocholorothiazide, chorthalidone, indapamide, and amiloride. More specifically, the diuretic is hydrocholorothiazide.

[0041] According to the invention, the ACEIs include more particularly lisinopril, enalapril, quinapril, ramipril, benazepril, captopril, cilazapril, fosinopril, imidapril, moexipril, trandolapril, or perindopril. According to a preferred embodiment, the ACEI is selected from the group consisting of enalapril, perindopril, ramipril, lisinopril and benazepril. More specifically, the ACEI is enalapril.

[0042] According to the invention, the ARBs include more particularly losartan, candesartan, irbesartan, telmisartan, valsartan, olmesartan, eprosartan and azilsartan. According to a preferred embodiment, the ARB is selected from the group consisting of losartan, candesartan, valsartan, olmesartan and azilsartan. More specifically, the ARB is valsartan.

[0043] Whenever appropriate, each of the active ingredients as identified herein also encompasses a pharmaceutically acceptable salt or solvate thereof.

[0044] Firibastat is chemically defined as (3S)-3-Amino-4[[(2S)-2-amino-4-sulfobutyl]disulfanyl)]butane-1-sulfonic acid or also named (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid). All those terms can thus be used herein interchangeably, and include zwitterionic form, pharmaceutically acceptable salt or solvate thereof, including a hydrate form. Firibastat can be a trihydrate form as disclosed in PCT/EP2011/067524. The term “firibastat” refers herein to (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid), a zwitterionic form, pharmaceutically acceptable salt or solvate thereof, including a hydrate form.

[0045] Firibastat can be referred as a homodimer of the selective aminopeptidase A (APA) inhibitor 3-amino 4-mercaptobutanesulfonic acid (also called EC33), generated by creating a disulfide bond between thiol groups of two 3-amino 4-mercaptobutanesulfonic acid molecules. Dimerisation affords a molecule more amenable to cross the gastro-intestinal and blood-brain barriers as a prodrug. On entry into the brain, firibastat is cleaved by brain reductases to generate two active molecules of EC33, which inhibit brain APA activity, block brain AngIII formation, and decrease BP.

[0046] (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) and use thereof as anti-hypertensive agent have been disclosed in the patent application WO2004/007441. The antihypertensive effects of firibastat treatment (500 mg twice a day) in mild to moderate hypertensive patients and in a diverse high-risk hypertensive population have been confirmed already (Azizi M., et al. A pilot double-blind randomized placebo-controlled crossover pharmacodynamic study of the centrally active aminopeptidase A inhibitor, firibastat, in hypertension. J Hypertens. 2019 August; 37(8):1722-1728; Ferdinand K C., et al. Efficacy and Safety of Firibastat, A First-in-Class Brain Aminopeptidase A Inhibitor, in Hypertensive Overweight Patients of Multiple Ethnic Origins. Circulation. 2019 Jul. 9; 140(2):138-146).

[0047] As mentioned above, references hereinafter to (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) or firibastat include the zwitterionic form and its pharmaceutically acceptable salts and solvates.

[0048] The person skilled in the art will recognize that firibastat may contain at least one positive and one negative charge so that firibastat includes zwitterionic forms thereof. In chemistry, a zwitterion (also called an inner salt), is a molecule with two or more functional groups, of which at least one has a positive and one has a negative electrical charge and the charges on the different functional groups balance each other out, and the molecule as a whole is electrically neutral.

[0049] The specialist in the art of organic chemistry will appreciate that many organic compounds can form complexes with solvents in which they are reacted or from which they are precipitated or crystallized. These complexes are known as “solvates”. For example, a complex with water is known as a “hydrate”. Solvates of the components (or active ingredients) (i)-(iii) are within the scope of the present invention. Solvates of (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) are within the scope of the present invention. Organic compounds can exist in more than one crystalline form. For example, crystalline form may vary from solvate to solvate. Thus, all crystalline forms of (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) or the pharmaceutically acceptable solvates thereof are within the scope of the present invention.

[0050] It will also be appreciated by the person skilled in the art that (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) may also be utilized in the form of pharmaceutically acceptable salts thereof. The pharmaceutically acceptable salts of (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) include conventional salts formed from pharmaceutically acceptable inorganic or organic acids or bases as well as quaternary ammonium salts and aminoacids. More specific examples of suitable acid salts include hydrochloric, hydrobromic, sulfuric, phosphoric, nitric, perchloric, fumaric, acetic, propionic, succinic, glycolic, formic, lactic, maleic, tartaric, citric, palmoic, malonic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, fumaric, toluenesulfonic, methanesulfonic, naphthalene-2-sulfonic, benzenesulfonic hydroxynaphthoic, hydroiodic, malic, steroic, tannic etc. Other acids such as oxalic, while not in themselves pharmaceutically acceptable, may be useful in the preparation of salts useful as intermediates in obtaining the compounds of the present invention and their pharmaceutically acceptable salts. More specific examples of suitable basic salts include sodium, lithium, potassium, magnesium, aluminium, calcium, zinc, N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, ethylenediamine, N-methylglucamine and procaine salts. More specific examples of suitable aminoacid salts include L- and D-forms of tryptophan, serine, cystine, valine, arginine, glycine, arginine, or lysine. A crystalline form of (3S,3S′) 4,4′-disulfanediylbis(3-aminobutane 1-sulfonic acid) with L-lysine and a process for the preparation of this crystalline form are disclosed in PCT/EP2013/072028.

[0051] In preferred embodiments, the indirectly or directly diseases related to HTN are selected from the group consisting of diseases of the heart, the peripheral and cerebral vascular system, the brain, the eye and the kidney. In particular, diseases include primary and secondary arterial HTN, ictus, myocardial ischaemia, heart failure, renal failure, myocardial infarction, peripheral vascular disease, diabetic proteinuria, Syndrome X or glaucoma. It may also include more particularly nephropathy, retinopathy or neuropathy in hypertensive diabetic patients. According to a particular embodiment, the indirectly or directly disease is heart failure.

[0052] Within the context of the invention, the term treatment denotes curative, symptomatic, and preventive treatment. Combinations or compositions of the invention can be used in subjects with existing HTN. The combination or the compositions of the invention will not necessarily cure the patient who has HTN but will control BP in a satisfactory manner, delaying or slowing thereby the progression or preventing thereby further complications of HTN, such as the directly or indirectly diseases as mentioned above. This will ameliorate consequently the patients' condition. The combination or the compositions of the invention can also be administered to those who do not have indirectly or directly diseases yet but who would normally develop the diseases or be at increased risk for said diseases, so that they will not develop said diseases. Treatment thus also includes delaying the development of indirectly or directly diseases in an individual who will ultimately develop said diseases or would be at risk for the diseases due to age, familial history, genetic or chromosomal abnormalities. By delaying the onset of the indirectly or directly diseases, compositions of the invention have prevented the individual from getting the diseases during the period in which the individual would normally have gotten the diseases or reduce the rate of development of the diseases or some of its effects but for the administration of compositions of the invention up to the time the individual ultimately gets the diseases.

[0053] The terms “patient,” “subject,” “individual,” and the like are used interchangeably herein, and refer to any human or non-human mammalian subject, including humans, laboratory, domestic, wild or farm animals. In certain non-limiting embodiments, the patient, subject or individual is a human. In other embodiments, the patient, subject or individual is a domestic animal, such as feline or canine subjects, a farm animal, such as but not limited to bovine, equine, caprine, ovine, and porcine subjects, wild animals (whether in the wild or in a zoological garden), research animals, such as mice, rats, rabbits, goats, sheep, pigs, dogs, cats, and the like, avian species, such as chickens, turkeys, songbirds, and the like, i.e., for veterinary medical use. Preferably the subject is a human patient whatever its sex (women or men) or age, generally an adult.

[0054] Surprisingly, the inventors identified a combination of at least three drugs, (i) firibastat, a brain APA inhibitor, (ii) a diuretic and (iii) a systemic RAS blocker, exerting their antihypertensive effects through distinct and complementary mechanisms of action and allowing a significant hypotensive effect. The unexpected advantage of this combination is illustrated by the potentiated BP lowering effect and the improved benefit observed over the dual combinations of each drug. The combination comprising (i) firibastat, (ii) a diuretic and (iii) a systemic RAS blocker, represents a very promising therapy to improve BP control, in patients with HTN and in particular in patients with difficult-to-treat HTN, and more specifically hypertensive patients not adequately controlled by a dual therapy, such as a diuretic and a systemic RAS blocker. More specifically, the combination comprising (i) firibastat, (ii) a diuretic and (iii) a systemic RAS blocker constitutes an alternative or adjunct therapy for hypertensive patients, and more specifically for high-risk for hypertensive patients, including those with salt-sensitivity, low plasma renin activity or sympathetic nervous system overactivity. Such patients are known to be associated with poor response to antihypertensive treatment with diuretics and/or systemic RAS blockers, used separately as single drug therapy or combined in a dual therapy.

[0055] In one embodiment, the present invention relates to a pharmaceutical combination, comprising (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group of systemic RAS blockers consisting of ACEIs and ARBs.

[0056] In a preferred embodiment, the diuretic is selected from the group consisting of hydrochlorothiazide, indapamide, furosemide and chlorthalidone. In a more preferred embodiment, the diuretic is hydrochlorothiazide.

[0057] In another preferred embodiment, the systemic RAS blocker is selected from the group of ACEIs consisting of enalapril, perindopril, ramipril and benazepril, or from the group of ARBs consisting of losartan, valsartan, candesartan and azilsartan. In a more preferred embodiment, the systemic RAS blocker is enalapril or valsartan.

[0058] In one embodiment, the present invention relates to a pharmaceutical combination, comprising (i) firibastat, (ii) hydrochlorothiazide and (iii) enalapril.

[0059] According to an embodiment of the invention, (i) firibastat, (ii) diuretic, and a systemic RAS blocker are administered simultaneously or sequentially, in the form of separate pharmaceutical compositions, each pharmaceutical composition comprising one of active ingredients (i)-(iii) in a pharmaceutically acceptable vehicle. In another embodiment, (i) firibastat, (ii) diuretic, and a systemic RAS blocker are administered simultaneously or sequentially, in the form of two separate pharmaceutical compositions, one pharmaceutical composition comprising one of said active ingredients selected from components (i)-(iii), and the other pharmaceutical composition comprising the other two of said active ingredients selected from components (i)-(iii), each pharmaceutical composition further comprising a pharmaceutically acceptable vehicle. In another embodiment, (i) firibastat, (ii) a diuretic, and a systemic RAS blocker are administered simultaneously in the form of a single pharmaceutical composition, said pharmaceutical composition further comprising a pharmaceutically acceptable vehicle. In the context of the present invention, the terms “pharmaceutical combination” refer to one or the other of these aspects.

[0060] According to the embodiment where (i) firibastat, (ii) diuretic, and a systemic RAS blocker are administered simultaneously or sequentially, in the form of two separate pharmaceutical compositions, the pharmaceutical composition comprising one of said active ingredients is preferably a pharmaceutical composition comprising firibastat, and the second pharmaceutical composition comprising the other two of said active ingredients selected from components (i)-(iii) is a pharmaceutical composition comprising the active ingredients (ii) and (iii), each of said pharmaceutical compositions further comprising a pharmaceutically acceptable vehicle.

[0061] The pharmaceutical combination or composition(s) according to the present invention is (or are) useful in the treatment of HTN or indirectly or directly related diseases. In treating the arterial HTN, preferred dosages for the active ingredients of the pharmaceutical combination according to the present invention are therapeutically effective dosages, especially those which are commercially available.

[0062] The pharmaceutical compositions of the invention as described above advantageously contain one or more supports or vehicles that are pharmaceutically acceptable. The term “pharmaceutically acceptable support” refers to carrier, adjuvant, or excipient acceptable to the subject from a pharmacological/toxicological point of view and to the manufacturing pharmaceutical chemist from a physical/chemical point of view regarding to composition, formulation, stability, subject acceptance and bioavailability.

[0063] More preferably, the composition(s) is (are) intended for oral administration, the pharmaceutically acceptable support or vehicle is thus suitable for an oral administration. As examples, mention may be made of saline, physiological, isotonic, buffered solutions, etc. compatible with pharmaceutical use and known to persons skilled in the art.

[0064] The pharmaceutical composition(s), as described above, can be prepared by mixing the three active ingredients, either all together or each one or two independently with a physiologically acceptable support, an excipient, a binder, a diluent, etc. The pharmaceutical composition(s) of the invention is (are) more specifically for a simultaneous sequential administration, preferably for simultaneous administration, of the three active ingredients (i)-(iii).

[0065] The pharmaceutical composition(s) is (are) then administered orally or non-orally, for instance via the parenteral, intravenous, cutaneous, nasal, rectal route or via aerosol delivery to the lungs. If the active ingredients are formulated independently, the corresponding formulations can be mixed together extemporaneously using a diluent and are then administered or can be administered independently of each other, either successively or sequentially.

[0066] Preferably, the composition(s) of the invention is (are) administered orally.

[0067] The pharmaceutical compositions of the invention include formulations, such as granules, powders, tablets, gel capsules, syrups, emulsions and suspensions, and also forms used for non-oral administration, for instance injections, sprays or suppositories.

[0068] The pharmaceutical forms can be prepared via the known conventional techniques.

[0069] The preparation of an orally administered solid pharmaceutical form will be performed by the following process: an excipient (for example lactose, sucrose, starch, mannitol, etc.), a disintegrant (for example calcium carbonate, calcium carboxymethylcellulose, etc.), a binder (for example starch, gum arabic, carboxymethylcellulose, polyvinylpyrrolidone, hydroxypropylcellulose, etc.) and a lubricant (for example talc, magnesium stearate, etc.) are, for example, added to the active ingredient(s) and the mixture obtained is then tabletted. If necessary, the tablet can be coated via the known techniques, in order to mask the taste (for example with cocoa powder, mint, etc.) or to allow enteric dissolution or sustained release of the active ingredients. Pharmaceutically acceptable colorants may be added. Pharmaceutical forms, such as tablets, powders, sachets and gel capsules can be used for an oral administration.

[0070] The liquid pharmaceutical forms for oral administration include solutions, suspensions and emulsions. The aqueous solutions can be obtained by dis-solving the active ingredient(s) in water, followed by addition of flavourings, colorants, stabilisers and thickener, if necessary. In order to improve the solubility, it is possible to add ethanol, propylene glycol or other pharmaceutically acceptable non-aqueous solvents. The aqueous suspensions for oral use can be obtained by dispersing the finely divided active ingredient(s) in water with a viscous product, such as natural or synthetic gums, resins, methylcellulose or sodium carboxymethylcellulose.

[0071] The pharmaceutical forms for injection can be obtained, for example, by the following process. The active ingredient(s) is (are) dissolved, suspended or emulsified either in an aqueous medium (for example distilled water, physiological saline, Ringer's solution, etc.) or in an oily medium (for example a plant oil, such as olive oil, sesameseed oil, cottonseed oil, corn oil, etc., or propylene glycol), with a dispersant, a preserving agent, an isotonicity agent and also other additives, such as, if desired, a solubilising agent or a stabiliser.

[0072] A pharmaceutical form for external use can be obtained from a solid, semi-solid or liquid composition containing the active ingredients. For example, to obtain a solid form, the active ingredients are treated, alone or as mixtures, with excipients and a thickener so as to convert them into powder. The liquid pharmaceutical compositions are prepared in substantially the same way as the forms for injection, as indicated previously. The semi-solid pharmaceutical forms are preferably in the form of aqueous or oily gels or in the form of pomade. These compositions may optionally contain a pH regulator and also other additives.

[0073] A therapeutically effective amount (i.e., an effective dosage) of a composition or of active ingredients of the invention is determined by one skilled in the art. More specifically, an effective amount is an amount that allows decreasing and maintaining BP as to control BP, in particular BP goal of <140/90 mmHg is recommended.

[0074] It will be appreciated that the amount of the active ingredients of the present invention required for use in treatment will vary with the nature of the condition being treated and the age and the condition of the subject and will be ultimately at the discretion of the attendant physician or veterinarian. In general, however, doses employed for adult human treatment will typically be in the range of 50 mg to 1500 mg per day or every other day, of firibastat. With respect to the second active ingredient, a diuretic, and to the third active ingredient selected from the group of systemic RAS blockers consisting of ACEIs and ARBs, doses employed for treatment will take into account the recommended dosages thereof.

[0075] According to a particular embodiment, the pharmaceutical combination of the invention comprises an amount of firibastat between 100 mg and 400 mg (e.g. 250 mg), an amount of hydrochorothiazide between 5 mg and 15 mg (e.g. 6.25 mg or 12.5 mg), and an amount of enalapril between 2.5 mg and 15 mg (e.g. 5 mg or 10 mg), either in one, two or three separate pharmaceutical composition(s).

[0076] According to another particular embodiment, the pharmaceutical combination of the invention comprises an amount of firibastat between 300 mg and 600 mg (e.g. 500 mg), an amount of hydrochorothiazide between 5 mg and 15 mg (e.g. 6.25 mg or 12.5 mg), and an amount of enalapril between 2.5 mg and 15 mg (e.g. 5 mg or 10 mg), either in one, two or three separate pharmaceutical composition(s).

[0077] According to another particular embodiment, the pharmaceutical combination comprises an amount of firibastat between 700 mg and 1200 mg (e.g. 1000 mg), an amount of hydrochorothiazide between 10 mg and 30 mg (e.g. 12.5 mg or 25 mg), and an amount of enalapril between 10 mg and 50 mg (e.g. 20 mg or 40 mg), either in one, two or three separate pharmaceutical composition(s).

[0078] The desired dose may conveniently be presented in a single dosage unit or several divided dosage units administered at appropriate intervals, for example as two, three, four or more sub-doses per day or every other day. The composition(s) according to the present invention may contain between 0.1-99% by weight of each active ingredient, conveniently from 30-95% by weight for tablets and capsules and 3-50% by weight for liquid preparations, the % are expressed with respect to the total amount of the said compositions. The frequency of administration of the active ingredients of the invention is between one and two administrations per day or every other day.

[0079] The relative proportions of the active ingredients of the pharmaceutical combination may vary upon the subject condition and also upon selected diuretic and systemic RAS blocker. For example, the weight ratio of firibastat relative to either hydrocholorthiazide or enalapril may range from 10/1 to 300/1 and preferably from 25/1 to 200/1.

[0080] The pharmaceutical combination can be included in a container, pack, or dispenser, also called a kit, together with instructions for administration. Corresponding instructions are given at the package insert concerning the combined administration of the respective active ingredients (i)-(iii) or pharmaceutical composition(s) comprising said active ingredients.

[0081] The present invention thus relates to kits that are suitable for the treatment by the methods or uses described above. These kits comprise a pharmaceutical combination, as defined above, containing (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group of systemic RAS blockers consisting of ACEIs and ARBs, for a simultaneous or sequential administration, preferably for simultaneous administration. More particularly, the kit comprises one or more (such as two or three) separate (either single or divided) dosage units of the active ingredients (i) to (iii) or of the pharmaceutical compositions comprising the active ingredients (i) to (iii), as defined above.

[0082] According to a particular embodiment, the kit of parts comprises a pharmaceutical combination, wherein (ii) the diuretic is selected from the group consisting of hydrochlorothiazide, indapamide, amiloride and chlorthalidone, and (iii) the blocker of the systemic renin-angiotensin system is selected from the group consisting of angiotensin I converting enzyme inhibitors consisting of enalapril, perindopril, ramipril and benazepril or from angiotensin II receptor type 1 antagonists the group consisting of losartan, valsartan, candesartan, irbesartan and azilsartan.

[0083] According to a more particular embodiment, the kit of the invention comprises a pharmaceutical combination, wherein (ii) the diuretic is hydrochlorothiazide and (iii) the blocker of the systemic renin-angiotensin system is enalapril.

[0084] According to another particular embodiment, the kit of the invention comprises a pharmaceutical combination, wherein (ii) the diuretic is hydrochlorothiazide and (iii) the blocker of the systemic renin-angiotensin system is valsartan.

[0085] According to another particular embodiment, the kit of parts comprises a pharmaceutical combination, wherein (ii) the diuretic is indapamide and (iii) the blocker of the systemic renin-angiotensin system is perindopril.

[0086] According to a further particular embodiment, the kit of parts comprises a pharmaceutical combination, wherein (ii) the diuretic is chlorthalidone and (iii) the blocker of the systemic renin-angiotensin system is azilsartan.

[0087] The separate dosage units of the kit are preferably made available together in one pack and either mixed prior to administration or sequentially administered.

[0088] For simultaneous administration as fixed composition (i.e. determined amounts and specific weight ratios between the said three active ingredients), a single pharmaceutical formulation may also be prepared which includes all three active ingredients (i)-(iii).

[0089] This invention is also directed to the use of (i) firibastat, (ii) a diuretic and (iii) a third active ingredient selected from the group consisting of ACEIs and ARBs, as defined above, in the manufacture of a medicine or one, two or three pharmaceutical composition, as defined above, intended for the treatment of arterial HTN or indirectly or directly related diseases.

[0090] The terms “simultaneous or sequential administration” of active ingredients to the same subject or patient, can be carried out over a period that may be up to 2 hours or even up to 6 hours. For example, the terms include (1) a simultaneous administration of the three active ingredients (i.e. the administration of all three active ingredients is carried out within a period of less than 10 minutes, e.g. from 30 seconds to 5 minutes long), (2) an administration of the three active ingredients separately but within a period of 3 hours, and (3) an administration of each of the three active ingredients separately every hour. According to a preferred embodiment, active ingredients are simultaneously co-administered according to (1).

[0091] The examples below of compositions according to the invention are given as non-limiting illustrations.

Examples

[0092] The amounts are expressed on a weight basis, unless otherwise stated.

Materials and Methods

Drugs

[0093] Firibastat was synthesized by PCAS (Limay, France). The angiotensin converting inhibitor (ACEI), enalapril was purchased from Sequoia Research (Pangbourne, United Kingdom). The diuretic, hydrochlorothiazide (HCTZ) was purchased from Sigma-Aldrich ((Saint-Louis, United-States).

[0094] The drugs were dissolved in sterile saline for in vivo per os by gavage administration.

Animals

[0095] Male deoxycorticosterone acetate (DOCA)-salt rats weighing 250 to 350 g were purchased from Charles River Laboratories (L'Arbresle, France). Animals were randomly assigned in each group with allocation concealment, and blinding procedures were used with coding systemAnimal care and surgical procedures were performed according to the Directive 2010/63/EU. The project was submitted to the appropriate ethics committee and authorization was obtained: 30 CEEA No 59, reference number 01962.01. Animals were kept under artificial light (12 h light/12 h dark cycle) with ad libitum access to a standard diet and saline water (0.9% NaCl, 0.2% KCl).

Surgical Methods and Mean Arterial BP Recording

[0096] Male DOCA-salt rats were anesthetized with 3% isoflurane (Iso-Vet®, Piramal, UK) for induction and 1.5-2% isoflurane for maintenance. A catheter (0.011″X.024″X.0065″) was inserted into the right femoral artery to monitor mean arterial blood pressure (MABP) and heart rate (HR). The catheters were tunneled subcutaneously to exit from the neck. Animals were allowed to recover from surgery for at least 48 h before MABP recording. Baseline MABP was recorded before drug administration during 30 minutes to 1 hour. One hour after the start of BP recording, firibastat (30 mg/kg), enalapril (5 or 10 mg/kg) and HCTZ (5 or 10 mg/kg) alone or in combination at different doses were administered to the conscious unrestrained rats by oral route. After compound administration, BP was monitored for 6 hours. MABP was calculated with the MatLab system (Phymep, Paris, France), consisting of a MatLab hardware unit and CHART software, running on a Macintosh computer. MABP and HR measurements were calculated by the BP signal.

[0097] For the chronic treatments, three groups of DOCA-salt rats were used. Saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) were administered orally by gavage every day. On day 8, a catheter was inserted into the right femoral artery to monitor mean arterial BP (MABP) as previously described. The animals were allowed to recover for at least 24 hours. On day 9, baseline MABP was recorded 30 minutes to 1 hour before drugs administration. Saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) were administered orally by gavage. MABP was then recorded at different time points after drug administration (5, 9 and 24 hours). For each time, recording period lasted 1 hour.

Plasma Collection for AVP Levels and Electrolytes Measurement

[0098] Rats were sacrificed by decapitation 5 hours after treatment (saline, enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) on day 10. Trunk blood (6-7 mL) was collected into chilled tubes containing 0.05 mL of 0.3M EDTA (pH 7.4) per mL of blood or 50 Units of heparin lithium per mL of blood on ice and centrifuged at 5000 rpm at 4° C. for 15 min.

AVP Radioimmunoassay

[0099] Plasma was acidified by adding 0.2 volumes of 3 M HCl and was stored at −80° C. until the AVP assay. Samples were thawed on ice and then centrifuged at 20,000×g for 20 min at 4° C. AVP was extracted from plasma by mixing 0.5 mL of the supernatant with 0.5 mL of 1% trifluoroacetic acid (TFA) and loading onto a Sep-Pak C18 cartridge (Waters, Mass., USA) previously washed with 2 mL 100% acetonitrile and equilibrated with 5 mL 1% TFA. The column was then washed with 3 mL of 1% TFA and AVP was eluted with 1.5 mL of 100% acetonitrile. The samples were lyophilized and dissolved in 0.35 mL of RIA buffer (19 mM NaH.sub.2PO.sub.4.Math.H.sub.2O, 81 mM Na.sub.2HPO.sub.4.Math.2H.sub.2O, 50 mM NaCl, 0.1% TritonX-100, 0.01% NaN.sub.3, 0.1% BSA). Plasma AVP levels were determined by radioimmunoassay (RIA) with 0.1 mL of plasma, using 0.1 mL of a polyclonal rabbit antiserum specific for AVP-[Arg8] (Peninsula Laboratories International, San Carlo, Calif., USA) displaying no cross reactivity with oxytocin at a dilution of 2:3, and 0.1 mL of [1251]-(Tyr2Arg8)-AVP 2000 Ci/mmol (PerkinElmer, Waltham, Mass., USA) as a tracer at 15,000 dpm, with incubation overnight at 4° C. We added 0.1 mL goat anti-rabbit IgG serum and 0.1 mL normal rabbit serum from Peninsula Laboratories International (San Carlo, Calif., USA) and incubated the resulting mixture for 2 h at room temperature. We then added 0.5 mL RIA buffer and centrifuged the tubes at 2,600×gat 4° C. for 20 minutes. The supernatant was removed, and the radioactivity of the precipitates was measured. The limit of detection of the AVP RIA was 0.2 pg per tube.

Plasma Electrolytes Measurement

[0100] Plasma sodium and potassium concentrations were determined with an electrolyte analyzer from Caretium Medical Instruments Co. (Shenzhen, China).

Statistical Analysis

[0101] Quantitative data are shown as means±SEM. Normality was assessed with the d'Agostino-Pearson test. ANOVA was performed after verification that the residuals were normally distributed. If normality was confirmed, comparisons between multiple groups were performed by one-way ANOVA, followed by Tukey, Holm-Sidak or Sidak's test for multiple comparisons. Differences were considered significant if the P value was <0.05. Statistical analyses were performed with Prism software (GraphPad Software).

RESULTS

[0102] Effects of acute oral administration of firibastat, enalapril and HCTZ alone or in combination on BP and HR in freely moving DOCA-salt rats.

[0103] Firibastat (30 mg/kg) administered alone induced a significant decrease in BP (−35.4±5.2 mmHg) whereas enalapril (10 mg/kg) or HCTZ (10 mg/kg) given alone did not induce any significant change in BP decrease in DOCA-salt rats (FIG. 1). Dual combinations of enalapril (5 mg/kg) plus HCTZ (5 mg/kg), firibastat (30 mg/kg) plus enalapril (10 mg/kg) or firibastat (30 mg/kg) plus HCTZ (10 mg/kg) significantly decreased arterial BP by 36.9±4.4 mmHg, 11.6±3.7 mmHg and 30.1±9.9 mmHg respectively (FIG. 1).

[0104] Concomitant oral administration of firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) significantly and markedly decreased MABP (FIG. 1) without significantly altering HR in conscious DOCA-salt rats (FIG. 2). A maximal decrease in MABP (−63.3±9.1 mmHg) was observed 5 hours after administration. The BP decrease induced by the triple combination of firibastat plus enalapril plus HCTZ was significantly different from that induced by each compound administered alone. Moreover, The BP decrease induced by the combination of firibastat plus enalapril plus HCTZ was significantly different from decreases induced by all the other dual combinations (firibastat plus enalapril, firibastat plus HCTZ and enalapril plus HCTZ).

[0105] In conclusion, combination of firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) potentiated the BP decrease induced by firibastat (30 mg/kg), even more that the dual combination enalapril (5 mg/kg) plus HCTZ (5 mg/kg). These surprising results suggest that the existence of a synergy of action between firibastat, enalapril and HCTZ in the DOCA-salt model, by blocking respectively the brain and the systemic RAS activities, and increasing diuresis, leading to a profound BP decrease.

Effects of 9-Day Chronic Oral Administration of Firibastat, Enalapril and HCTZ in Combination on BP and HR in Freely Moving DOCA-Salt Rats

[0106] We studied in alert DOCA-salt rats the effects on BP and HR of oral daily 9-day chronic administration of the dual combination of enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or the triple combination of firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg). On day 9, we studied the time course of the effects of oral administration of these combinations on BP during 24 hours in alert DOCA-salt rats.

[0107] After 5 and 9 hours, concomitant oral administration of enalapril (5 mg/kg) plus HCTZ (5 mg/kg) or firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) significantly and markedly decreased MABP (FIG. 3) without significantly altering HR in conscious DOCA-salt rats (FIG. 4). The decrease in MABP induced by the triple combination of firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) was maximal 5 hours after administration and persisted after 9 hours, with significant decreases in MABP of 61.9±6.2 mmHg and 49.3±7.4 mmHg (P<0.0001), respectively (FIG. 3). After 24 hours, no decrease on BP was observed.

[0108] Five hours after administration, the BP decrease induced by the triple combination of firibastat (30 mg/kg) plus enalapril (5 mg/kg) plus HCTZ (5 mg/kg) was significantly different from that induced by the dual combination of enalapril (5 mg/kg) plus HCTZ (5 mg/kg) (61.9±6.2 mmHg and 31.3±8.2 mmHg (P<0.05), respectively).

[0109] As in acute treatment, 9-day chronic treatment with the triple combination of firibastat (30 mg/kg/day) plus enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day) potentiated the BP decrease induced by firibastat (30 mg/kg/day). The synergy of action was even more marked when comparing the effects to the dual combination of enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day). These results demonstrate also the absence of tolerance to the antihypertensive effect of triple combination of firibastat (30 mg/kg/day) plus enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day) after repeated administrations.

[0110] Overall, these data indicate the existence, even after repeated administration, of a synergy of action between firibastat, enalapril and HCTZ to regulate BP in hypertensive DOCA-salt rats.

[0111] Blocking together brain RAS hyperactivity, systemic RAS activity and increasing diuresis with a triple combination of firibastat, enalapril and HCTZ represents a novel and original therapeutic treatment of HTN enabling further BP decrease in in hypertensive patients, more specifically on difficult-to-treat and resistant hypertensive patients.

Effect of 10-Day Chronic Oral Administration of Firibastat, Enalapril and HCTZ in Combination on Plasma Arginine-Vasopressin (AVP) Levels in Conscious Hypertensive DOCA-Salt Rats

[0112] On day 10, levels of plasma AVP (known as the anti-diuretic hormone) in DOCA-salt rats which received chronic oral saline treatment were 28.2±3.3 pg/mL. The plasma AVP levels in DOCA-salt rats, 5 hours after repeated daily oral administrations of the dual combination of enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day) or the triple combination of firibastat (30 mg/kg/day) plus enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day) were increased by 107% and 40% (58.3±4.0 μg/mL and 39.6±5.3 μg/mL vs 28.2±3.3 μg/mL, respectively) when compared to DOCA-salt rats receiving chronic saline (FIG. 5).

[0113] The difference in plasma AVP levels between DOCA-salt rats receiving chronic treatment with the dual combination of enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day) and DOCA-salt rats receiving chronic treatment with the triple combination of firibastat (30 mg/kg/day) plus enalapril (5 mg/kg/day) plus HCTZ (5 mg/kg/day) was 18.8 μg/mL. The addition of firibastat to the dual combination of enalapril and HCTZ reduced by 62% the increase in plasma AVP levels observed in DOCA-salt rats that received this dual combination (One-way ANOVA followed by Tukey's test, P<0.05).