Glucocorticoid receptor modulator relacorilant with paclitaxel patent granted
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.
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, 2026GovPing 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.
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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