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Glucocorticoid receptor modulator relacorilant with paclitaxel patent granted

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Summary

USPTO granted patent US12589094B2 to Corcept Therapeutics Incorporated on March 31, 2026, covering methods of co-administering glucocorticoid receptor modulator relacorilant with paclitaxel by reducing paclitaxel dose to approximately half when used together. The patent addresses drug-drug interaction management, noting that despite in vitro predictions of 5-fold increased paclitaxel exposure, in vivo co-administration showed only 80% increase, enabling a safer combination therapy for treating cancers such as ovarian and pancreatic.

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What changed

USPTO granted patent US12589094B2 to Corcept Therapeutics for a method of treating cancer by co-administering relacorilant with paclitaxel while reducing the paclitaxel dose to approximately half the standard dose. The patent discloses that relacorilant inhibits CYP2C8 and CYP3A4 enzymes in vitro, which would theoretically increase paclitaxel plasma exposure more than 5-fold, but surprisingly the actual increase was only about 80%. Inventors Hazel Hunt and Joseph Custodio identified that this reduced dosing regimen enables safe co-administration for ovarian or pancreatic cancer treatment.\n\nPharmaceutical companies developing relacorilant or paclitaxel products should review this patent to understand the claimed combination therapy and dosing methodology. Generic manufacturers of paclitaxel should be aware that co-administration with relacorilant may trigger patent claims. Healthcare providers treating patients with both drugs should note the recommended 50% paclitaxel dose reduction when used concurrently. No compliance deadlines apply as this is a granted patent rather than a regulatory requirement.

Archived snapshot

Mar 31, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Grants

Concomitant administration of glucocorticoid receptor modulator relacorilant and paclitaxel, a dual substrate of CYP2C8 and CYP3A4

Grant US12589094B2 Kind: B2 Mar 31, 2026

Assignee

Corcept Therapeutics Incorporated

Inventors

Hazel Hunt, Joseph Custodio

Abstract

Many drugs useful in treating cancer are metabolized by CYP2C8 enzymes, by CYP3A4 enzymes, or both. The effects of concomitant administration of relacorilant and paclitaxel, a drug used to treat cancer that is a substrate for both CYP2C8 and CYP3A4, are disclosed herein. Relacorilant potently inhibited CYP2C8 and CYP3A4 in in vitro tests, indicating that co-administration of relacorilant and paclitaxel would increase paclitaxel plasma exposure more than 5-fold in vivo, requiring significant reductions in paclitaxel doses when co-administering paclitaxel with relacorilant. Surprisingly, paclitaxel plasma exposure increased only by about 80% instead of the expected more than 5-fold increase expected with concomitant relacorilant and paclitaxel administration. Applicant discloses safe methods of co-administering relacorilant and paclitaxel by reducing the dose of paclitaxel to about half the paclitaxel dose used when paclitaxel is administered alone. Relacorilant and such reduced doses of paclitaxel may be co-administered to treat cancer, e.g., ovarian or pancreatic cancer.

CPC Classifications

A61K 31/416 A61K 31/445 A61K 31/451 A61K 31/4725 A61K 31/337 A61P 35/00

Filing Date

2024-02-28

Application No.

18590002

Claims

13

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Last updated

Classification

Agency
USPTO
Published
March 31st, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US12589094B2

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers Healthcare providers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Pharmaceutical Patent Protection Combination Drug Therapy Drug-Drug Interaction Management
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

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