Treatment and prognostic monitoring of non-cancerous proliferation disorders using hedgehog pathway inhibitors

• US 9,968,600 B2
• Filed: 01/31/2017
• Issued: 05/15/2018
• Est. Priority Date: 04/17/2013
• Status: Active Grant

• Current Assignee: Inhibitor Therapeutics, Inc. (Mayne Pharma)
• Original Assignee: Inhibitor Therapeutics, Inc. (Mayne Pharma)
• Inventors: Virca, Nicholas J., O'Donnell, Jr., Francis E.
• Primary Examiner(s): Rao, Savitha M
• Application Number:
  US15/420,283
• Publication Number:
  US 20170136012A1
• Time in Patent Office: 469 Days
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 31/496 Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
• CPC Class Codes: A61K 31/519 ortho- or peri-condensed with heterocyclic rings
• CPC Class Codes: A61K 31/58 containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin digitoxin A61K31/7048
• CPC Class Codes: A61K 33/24 Heavy metals; Compounds thereof
• CPC Class Codes: A61K 33/243 Platinum; Compounds thereof
• CPC Class Codes: A61K 45/06 Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• CPC Class Codes: A61K 9/0053 Mouth and digestive tract, i.e. intraoral and peroral administration rectal administration A61K9/0031
• CPC Class Codes: A61K 9/4866 Organic macromolecular compounds
• CPC Class Codes: A61P 13/08 of the prostate
• CPC Class Codes: A61P 31/00 Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: G01N 2333/96455 Kallikrein (3.4.21.34; 3.4.21.35)
• CPC Class Codes: G01N 33/57484 involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites

Abstract

The present invention concerns methods for treating a proliferation disorder, such as prostate cancer, basal cell carcinoma, lung cancer, and other cancers, using an inhibitor of the Hedgehog pathway (HhP); and methods for monitoring subjects undergoing such treatments based on biomarkers and other criteria predictive of efficacy.

Claims

1. A method for treating a non-cancerous proliferation disorder in a subject, comprising orally administering a composition comprising a Hedgehog pathway (HhP) inhibitor to the subject, wherein the HhP inhibitor comprises itraconazole, or a pharmaceutically acceptable salt prodrug, stereoisomer, or active metabolite thereof, wherein:

(a) the composition is orally administered in an effective amount to achieve a plasma trough level of at least about 1,000 ng/mL of the HhP inhibitor;

or (b) the composition is orally administered at a dose in the range of 100 mg to 600 mg HhP inhibitor per day.

2. The method of claim 1, wherein the HhP inhibitor comprises itraconazole, or a pharmaceutically acceptable salt, or stereoisomer thereof.

3. The method of claim 1, wherein the composition comprises a solid dispersion of the HhP inhibitor and at least one polymer having one or more acidic functional groups;

and wherein the composition is orally administered at a dose in the range of 100 mg to 600 mg of the HhP inhibitor per day.

4. The method of claim 2, wherein the composition is in the form of a capsule or powder, and wherein the composition is orally administered at a dose of 50 mg of the itraconazole, or a pharmaceutically acceptable salt, prodrug, stereoisomer, or active metabolite thereof, twice per day.

5. The method of claim 3, wherein the composition is in the form of a capsule.

6. The method of claim 1, wherein the composition is administered in an effective amount to achieve a plasma trough level of at least 1,000 ng/mL of the HhP inhibitor.

7. The method of claim 1, wherein the composition is administered in an effective amount to achieve a plasma trough level of at least about 1,000 ng/mL of the HhP inhibitor after about 4 weeks of initiation of treatment with the HhP inhibitor.

8. The method of claim 1, wherein the composition is administered in an effective amount to achieve a plasma trough level of at least about 1,000 ng/mL of the HhP inhibitor within about 2 weeks after initiation of treatment, and to maintain the plasma trough level of at least about 1,000 ng/mL of the HhP inhibitor for the duration of the treatment.

9. The method of claim 1, further comprising measuring the plasma level of the HhP inhibitor, or a metabolite thereof, in the subject one or more times.

10. The method of claim 9, wherein said measuring is carried out one or more times about 4 weeks after initiation of treatment with the HhP inhibitor.

11. The method of claim 1, further comprising measuring the plasma level of the HhP inhibitor, or a metabolite thereof, one or more times in a period of time from about 4 weeks to about 12 weeks.

12. The method of claim 11, further comprising increasing a subsequent dose of the HhP inhibitor if the plasma trough level of at least about 1,000 ng/mL of the HhP inhibitor is not maintained.

13. The method of claim 11, further comprising reducing a subsequent dose of an HhP inhibitor if the plasma trough level at about 4 weeks is at least 1000 ng/mL and the patient is experiencing one or more side effects.

14. The method claim 3, wherein the polymer is a polycarboxylic acid polymer.

15. The method of claim 14, wherein the polycarboxylic acid polymer is hypromellose phthalate (hydroxypropyl methylcellulose phthalate).

16. The method of claim 1, wherein the non-cancerous proliferation disorder is smooth muscle cell proliferation, systemic sclerosis, cirrhosis of the liver, adult respiratory distress syndrome, idiopathic cardiomyopathy, lupus erythematosus, retinopathy, cardiac hyperplasia, benign prostatic hyperplasia, ovarian cyst, pulmonary fibrosis, endometriosis, fibromatosis, hamartomas, lymphangiomatosis, sarcoidosis, colorectal polyps, or desmoid tumors.

17. The method of claim 1, wherein the non-cancerous proliferation disorder is a hyperproliferation of cells in the skin, Reiter'"'"'s syndrome, pityriasis rubra pilaris, scleroderma, seborrheic keratoses, intraepidermal nevi, common wart, or benign epithelial tumor.

18. The method of claim 1, wherein the non-cancerous proliferation disorder is a hyper-proliferative variant of a disorder of keratinization.

19. The method of claim 1, wherein the non-cancerous proliferation disorder is colorectal polyps.