IP Library Granted Patent US 12,336,985
Granted Patent B2
US 12,336,985 · App. 18/653,070 · Granted Jun 24, 2025

Methods for shrinking pituitary tumors

Inventor: Andreas Moraitis (Sunny Isles Beach, FL)
Assignee: Corcept Therapeutics Incorporated
A61K31/444A61P35/00A61B17/3205A61N5/10
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Quick Facts
Patent No.
US 12,336,985
App. No.
18/653,070
Granted
Jun 24, 2025
Kind
B2
Abstract

Pituitary tumors may be reduced in size by administration of relacorilant. Pituitary tumors include, without limitation, non-secreting tumors, hormone-secreting tumors, adenomas, and carcinomas. Relacorilant administration may be effective to reduce hormone secretion from a hormone-secreting pituitary tumor, e.g., to reduce adrenocorticotrophic hormone (ACTH) secretion. A pituitary tumor may be imaged before and/or after relacorilant administration. Relacorilant may be administered independent of surgery, and before, during, or after surgery to treat a pituitary tumor. Relacorilant may aid or improve surgical outcomes, and may reduce the size or growth of pituitary tumor tissue before surgery, and any tumor tissue remaining following surgical treatment. Relacorilant may be orally administered for the treatment of pituitary tumors. Relacorilant may be orally administered to a fasted patient, or to a fed patient. Relacorilant may be administered in conjunction with other pituitary tumor targeting treatments, including surgical treatments, radiation treatments, chemotherapy for carcinomas, and other pharmaceutical treatments.

Claims (19)

1. A method of reducing the size of a visible pituitary macroadenoma tumor in a patient suffering from said tumor, the tumor not having been treated with radiation, the method comprising imaging said visible pituitary macroadenoma tumor effective to determine a first size of said tumor, and then administering for three months to the patient daily oral doses of between about 100 milligrams (mg) and about 200 mg of relacorilant, where relacorilant is ((R)-(1-(4-fluorophenyl)-6-((1-methyl-1H-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1H-pyrazolo[3,4-g]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-yl)methanone), which has the following structure:

effective to reduce the size of the visible pituitary macroadenoma tumor from said first size of the visible pituitary macroadenoma tumor to a second size of the visible pituitary macroadenoma tumor, wherein said second size of the visible pituitary macroadenoma tumor is smaller than the first size of the visible pituitary macroadenoma tumor.

2. The method of claim 1 , further comprising determining that said patient suffers from a symptom of Cushing's syndrome.

3. The method of claim 1 , wherein said daily oral dose is selected from 100 mg, 150 mg, and 200 mg of relacorilant.

4. The method of claim 1 , further comprising measuring said visible pituitary macroadenoma tumor following relacorilant administration, wherein said measuring comprises a second imaging of the visible pituitary macroadenoma tumor.

5. The method of claim 4 , further comprising application of a further treatment directed to said visible pituitary macroadenoma tumor following said second imaging of the visible pituitary macroadenoma tumor.

6. The method of claim 5 , wherein said further treatment directed to said visible pituitary macroadenoma tumor comprises surgical treatment.

7. The method of claim 1 , wherein said visible pituitary macroadenoma tumor is a non-secreting pituitary tumor.

8. The method of claim 1 , wherein said visible pituitary macroadenoma tumor is a hormone-secreting tumor, wherein said hormone-secreting tumor secretes a first amount of hormone, and said treatment is effective to reduce the size of the visible pituitary macroadenoma tumor from said first size to said second size, and to reduce hormone secretion from said visible pituitary macroadenoma tumor from said first amount to a second amount of hormone secretion that is less than said first amount of hormone secretion.

9. The method of claim 1 , wherein said relacorilant administration comprises daily oral administration of relacorilant in one or more single unit dosage forms each containing an amount of relacorilant selected from 20 milligrams (mg), 50 mg, 100 mg, 150 mg, and 200 mg of relacorilant.

10. The method of claim 1 , wherein said administration of relacorilant comprises oral administration of relacorilant to a fasted patient.

11. The method of claim 10 , wherein said fasted patient is a patient who has not eaten a meal or otherwise ingested food for at least two hours prior to the administration of relacorilant.

12. The method of claim 1 , wherein said administration of relacorilant comprises oral administration of relacorilant to a fed patient.

13. The method of claim 12 , wherein said fed patient is a patient who has begun eating a meal about 30 minutes or less prior to the administration of relacorilant.

14. The method of claim 12 , wherein a fed patient is a patient who has begun eating a meal about one hour or less prior to the administration of relacorilant.

15. The method of claim 1 , wherein said administration of relacorilant comprises relacorilant administration prior to surgery for resection of the visible pituitary macroadenoma tumor.

16. The method of claim 1 , wherein said administration of relacorilant comprises relacorilant administration following surgery for resection of the visible pituitary macroadenoma tumor.

17. The method of claim 16 , wherein said relacorilant administration following surgery for resection of the visible pituitary macroadenoma tumor is effective to reduce the size of tumor tissue remaining in the patient following said surgical treatment from an unresected size to a smaller remaining size of tumor tissue, or to reduce the rate of growth of tumor tissue remaining in the patient following said surgical treatment from a first tumor growth rate to a second tumor growth rate smaller than said first tumor growth rate.

18. The method of claim 17 , further comprising administration of radiation treatment or cancer chemotherapy treatment, or both, to said patient receiving relacorilant administration following surgery for resection of the visible pituitary macroadenoma tumor.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2024
From: MORAITIS, ANDREAS
To: CORCEPT THERAPEUTICS INCORPORATED
Reel/Frame 067311/0956 →
Continuity (4)
Continuation 17185133 · Feb 25, 2021
Continuation 16678988 · Nov 8, 2019
Provisional Application 62758477 · Nov 9, 2018
Related Publication 20240277686A1 · Aug 22, 2024
References Cited (39)
US 8859774B2 · Hunt et al. · 2014 [cited by applicant]
US 9273047B2 · Hunt et al. · 2016 [cited by applicant]
US 9707223B2 · Hunt et al. · 2017 [cited by applicant]
US 9956216B2 · Hunt et al. · 2018 [cited by applicant]
US 10946005B2 · Moraitis · 2021 [cited by applicant]
US 20150080389A1 · Hunt et al. · 2015 [cited by applicant]
US 20180125856A1 · Moraitis et al. · 2018 [cited by applicant]
JP 2015517580A1 · 2015 [cited by applicant]
JP 2018507226A · 2018 [cited by applicant]
WO 2016061583A1 · 2016 [cited by applicant]
WO 2016140867A1 · 2016 [cited by applicant]
WO 2017151613A1 · 2017 [cited by applicant]
Fleseriu (Fleseriu, M., et al., Changes in Plasma ACTH Levels and Corticotroph Tumor Size in Patients With Cushing's Disease During Long-term Treatment With the Glucocorticoid Receptor Antagonist Mifepristone, J. Clin. … [cited by examiner]
Hunt (Hunt, H.J, et al., Identification of the Clinical Candidate (R)-(1-(4-Fluorophenyl)-6-((1-methyl-1H-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1H-pyrazolo[3,4-g]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-y… [cited by examiner]
“A Study of the Efficacy and Safety of Relacorilant (GRACE)”, ClinicalTrials.gov, Available Online at: https://clinicaltrials.gov/ct2/history/NCT03697109?V_2=View#StudyPageTop, NCT03697109,, Oct. 31, 2018, 7 pages. [cited by applicant]
U.S. Appl. No. 16/678,988 , Advisory Action, Mailed on Dec. 1, 2020, 3 pages. [cited by applicant]
U.S. Appl. No. 16/678,988 , Final Office Action, Mailed on Sep. 24, 2020, 13 pages. [cited by applicant]
U.S. Appl. No. 16/678,988 , Non-Final Office Action, Mailed on Apr. 14, 2020, 10 pages. [cited by applicant]
U.S. Appl. No. 16/678,988 , Notice of Allowance, Mailed on Feb. 4, 2021, 9 pages. [cited by applicant]
U.S. Appl. No. 17/185,133 , Final Office Action, Mailed on Sep. 21, 2023, 19 pages. [cited by applicant]
U.S. Appl. No. 17/185,133 , Non-Final Office Action, Mailed on Mar. 30, 2023, 14 pages. [cited by applicant]
U.S. Appl. No. 17/185,133 , Notice of Allowance, Mailed on Mar. 28, 2024, 11 pages. [cited by applicant]
Check et al., “Evidence that Mifepristone, A Progesterone Receptor Antagonist, Can Cross the Blood Brain Barrier and Provide Palliative Benefits for Glioblastoma Multiforme Grade IV”, Anticancer Research, vol. 34, No. 5… [cited by applicant]
Check et al., “Mifepristone Causing Complete Remission of Rapidly Advancing Leukemia with Measurement of Progesterone-Induced Blocking Factor”, Anticancer Research, vol. 34, No. 5, May 2014, pp. 2413-2416. [cited by applicant]
Cuevas-Ramos et al., “Treatment of Cushing's Disease: A Mechanistic Update”, Journal of Endocrinology, vol. 223, No. 2, Nov. 2014, pp. R19-R39. [cited by applicant]
European Patent Application No. 19881977.3 , Extended European Search Report, Mailed on Jul. 20, 2022, 8 pages. [cited by applicant]
Fleseriu et al., “Changes in Plasma ACTH Levels and Corticotroph Tumor Size in Patients with Cushing's Disease During Long-Term Treatment with the Glucocorticoid Receptor Antagonist Mifepristone”, The Journal of Clinica… [cited by applicant]
Fleseriu et al., “Mifepristone, a Glucocorticoid Receptor Antagonist, Produces Clinical and Metabolic Benefits in Patients with Cushing's Syndrome”, The Journal of Clinical Endocrinology & Metabolism, vol. 97, No. 6, Ma… [cited by applicant]
Hunt et al., “Assessment of Safety, Tolerability, Pharmacokinetics, and Pharmacological Effect of Orally Administered CORT125134: An Adaptive, Double-Blind, Randomized, Placebo-Controlled Phase 1 Clinical Study”, Clinic… [cited by applicant]
Hunt et al., “Identification of the Clinical Candidate (R)-(1-(4-Fluorophenyl)-6-((1-Methyl-1H-Pyrazol-4-yl)Sulfonyl)-4,4a,5,6,7,8-Hexahydro-1H-Pyrazolo[3,4-g]lsoquinolin-4a-yl)(4-(Trifluoromethyl)Pyridin-2-yl)Methanone… [cited by applicant]
Japanese Patent Application No. JP2021-525281 , Office Action, Mailed on May 31, 2022, 6 pages. [cited by applicant]
Kovacs et al., “Glucocorticoid Receptor Expression in Nontumorous Human Pituitaries and Pituitary Adenomas”, Endocrine Pathology, vol. 11, No. 3, Sep. 2000, pp. 267-275. [cited by applicant]
Langlois et al., “Recent Progress in the Medical Therapy of Pituitary Tumors”, Endocrinology and Metabolism, vol. 32, No. 2, May 19, 2017, pp. 162-170. [cited by applicant]
International Patent Application No. PCT/US2019/060548 , International Preliminary Report on Patentability, Mailed on May 20, 2021, 7 pages. [cited by applicant]
International Patent Application No. PCT/US2019/060548 , International Search Report and Written Opinion, Mailed on Apr. 10, 2020, 11 pages. [cited by applicant]
Russian Patent Application No. 2021116258 , Office Action, Mailed on Feb. 25, 2022, 7 pages. [cited by applicant]
Terzolo et al., “SUN-463 Tumor Shrinkage with Preoperative Relacorilant Therapy in Two Patients with Cushing Disease Due to Pituitary Macroadenomas”, Journal of the Endocrine Society, vol. 3, No. 1, Apr. 30, 2019, 2 pag… [cited by applicant]
Touat et al., “Successful Treatment of Multiple Intracranial Meningiomas with the Antiprogesterone Receptor Agent Mifepristone (RU486)”, Acta Neurochirurgica, vol. 156, No. 10, Oct. 2014, pp. 1831-1835. [cited by applicant]
Winters et al., “Addison's Disease and Pituitary Enlargement”, The American Journal of the Medical Sciences, vol. 349, No. 6, Jun. 2015, pp. 526-529. [cited by applicant]