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Luveltamab tazevibulin - Sutro Biopharma

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Drug Profile

Luveltamab tazevibulin - Sutro Biopharma

Alternative Names: anti-FolRa ADC STRO-002; anti-FolRalpha ADC STRO-002; FolR-alpha-ADC-Sutro-Biopharma; Luvelta; STRO-002

Latest Information Update: 16 Dec 2024

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At a glance

  • Originator Sutro Biopharma
  • Developer Gynecologic Oncology Group; Sutro Biopharma; Tasly Biopharmaceuticals
  • Class Amides; Antibodies; Antineoplastics; Drug conjugates; Immunoconjugates; Immunotoxins; Indoles
  • Mechanism of Action Tubulin inhibitors
  • Orphan Drug Status

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

    Yes - Acute myeloid leukaemia
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Phase II/III Ovarian cancer
  • Phase II Non-small cell lung cancer
  • Phase I/II Acute myeloid leukaemia; Solid tumours
  • Phase I Endometrial cancer; Fallopian tube cancer; Peritoneal cancer

Most Recent Events

  • 10 Dec 2024 Luvelta plans for an Accelerated Approval application in mid-2027
  • 10 Dec 2024 Adverse events and efficacy data from a phase II/III REFRaME-O1 trials in Ovarian cancer released by Sutro Biopharma
  • 13 Nov 2024 Luveltamab tazevibulin - Sutro Biopharma is available for licensing as of 13 Nov 2024. http://www.sutrobio.com

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