Estrogen Dependent Uterine Fibroids Therapeutics

1. Orgovyx patent expiration

Treatment: Treatment of adult patients with advanced prostate cancer; Treatment of adult patients with advanced prostate cancer that is sex-hormone-dependent; Treatment of adult patients with advanced prostate c...

ORGOVYX's oppositions filed in EPO
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance.
US7300935 SUMITOMO PHARMA AM Thienopyrimidine compounds and use thereof
Jan, 2029

(3 years from now)

US11795178 SUMITOMO PHARMA AM Compositions of thienopyrimidine derivatives
Sep, 2033

(7 years from now)

US12325714 SUMITOMO PHARMA AM Compositions of thienopyrimidine derivatives
Sep, 2033

(7 years from now)

US8058280 SUMITOMO PHARMA AM Substituted thieno[2,3-d]pyrimidin-2,4-dione compounds and uses thereof
Jan, 2026

(19 days from now)

These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US11583526 SUMITOMO PHARMA AM Treatment of prostate cancer
Sep, 2037

(11 years from now)

US8735401 SUMITOMO PHARMA AM Thienopyrimidine compounds and use thereof
Feb, 2024

(1 year, 11 months ago)

US12336990 SUMITOMO PHARMA AM Treatment of prostate cancer
Sep, 2037

(11 years from now)

US12144809 SUMITOMO PHARMA AM Treatment of prostate cancer
Sep, 2037

(11 years from now)

US10449191 SUMITOMO PHARMA AM Treatment of prostate cancer
Sep, 2037

(11 years from now)

US10786501 SUMITOMO PHARMA AM Treatment of prostate cancer
Sep, 2037

(11 years from now)

US12097198 SUMITOMO PHARMA AM Treatment of prostate cancer
Sep, 2037

(11 years from now)

US10350170 SUMITOMO PHARMA AM Solid preparation
Feb, 2036

(10 years from now)




Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Dec 18, 2025

Drugs and Companies using RELUGOLIX ingredient

NCE-1 date: 18 December, 2024

Market Authorisation Date: 18 December, 2020

Dosage: TABLET

More Information on Dosage

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