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A Phase 1 Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of STRO-002, an Anti-Folate Receptor Alpha Antibody Drug Conjugate, in Combination With Bevacizumab in Patients With Advanced Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers)

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A Phase 1 Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of STRO-002, an Anti-Folate Receptor Alpha Antibody Drug Conjugate, in Combination With Bevacizumab in Patients With Advanced Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers)

Status: Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 18 Sep 2024

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At a glance

  • Drugs Bevacizumab (Primary) ; Luveltamab tazevibulin (Primary)
  • Indications Adenocarcinoma; Fallopian tube cancer; Ovarian cancer; Peritoneal cancer
  • Focus Adverse reactions; First in man
  • Sponsors Sutro Biopharma

    • Most Recent Events

    • 14 Sep 2024 According to Sutro Biopharma media release, the expansion phase of the study is ongoing at the recommended phase 2 dose (RP2D) of luvelta (4.3 mg/kg) in combination with bevacizumab (15 mg/kg) with an additional 23 patients enrolled to date. 18 patients were enrolled; one patient remains on treatment.
    • 14 Sep 2024 According to Sutro Biopharma media release, company looking forward to sharing initial results from expansion phase in the first half of 2025.
    • 14 Sep 2024 Results published in a Sutro Biopharma media release

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