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A Study of STRO-002, an Anti-Folate Receptor Alpha Antibody Drug Conjugate, in Combination With Bevacizumab in Epithelial Ovarian Cancer

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NCT05200364

Sponsored by Sutro Biopharma, Inc. (industry) · STRO — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Na · None · Treatment
Enrollment
58actual
Sites
6
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Terminated Early

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-03-22actualWhen the study began enrolling
Primary completion2025-06-01actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-06-01actualThe whole study's end, after follow-up
First posted2022-01-20actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-09-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Ovarian Cancer
  • Ovarian Carcinoma
  • Ovary Cancer
  • Fallopian Tube Cancer
  • Primary Peritoneal Carcinoma

Interventions

  • Drug: STRO-002
  • Drug: Bevacizumab — also filed as Avastin

Primary outcomes

what the primary-completion date above is the date OF
Part 1 - Safety and tolerability of STRO-002/bevacizumab as a combination therapy
measured From baseline through end of study (approximately 24 months)
Part 1 - Determine the recommended phase 2 dose (RP2D) of STRO-002/bevacizumab
measured From baseline through end of study (approximately 24 months)

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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