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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: 20 Aug 2024

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At a glance

  • Originator Takeda
  • Developer ASKA 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

  • 14 Aug 2024 The UK's NICE recommends Relugolix (ORGOVYX®) as the first oral ADT treatment for hormone sensitive prostate cancer in England
  • 12 Mar 2024 Launched for Prostate cancer (Late-stage disease, Metastatic disease) in Canada (PO)
  • 28 Feb 2024 No recent reports of development identified for phase-I development in Prostate-cancer(Combination therapy, Hormone refractory, Metastatic disease, Second-line therapy or greater) in USA (PO, Tablet)

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