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Relugolix - Sumitomo Pharma America/Takeda

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Drug Profile

Relugolix - Sumitomo Pharma America/Takeda

Alternative Names: MVT-601 - Sumitomo Pharma America/Takeda; ORGOVYX; Relumina; RVT 601; T-1331285; TAK-385

Latest Information Update: 17 Jun 2025

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At a glance

  • Originator Takeda
  • Developer ASKA Pharmaceutical; Qilu Pharmaceutical; Sumitomo Pharma America; Takeda; Takeda Oncology
  • Class Analgesics; Antineoplastics; Fluorobenzenes; Ketones; Pyridazines; Pyrimidines; Small molecules; Thiophenes; Urea compounds
  • Mechanism of Action LHRH receptor antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes

Highest Development Phases

  • Marketed Prostate cancer
  • Registered Endometriosis; Uterine leiomyoma
  • Phase II Pain
  • No development reported Solid tumours

Most Recent Events

  • 05 Jun 2025 Knight Therapeutics in-licenses Relugolix from Sumitomo Pharma America in Canada
  • 28 Feb 2025 Phase-III clinical trials in Uterine leiomyoma in China (PO) (NCT06671548)
  • 13 Feb 2025 Efficacy, pharmacokinetics and adverse events data from a phase I trial in Prostate cancer presented at the 2025 Genitourinary Cancers Symposium (ASCO-GeCS-2025)

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