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Mirvetuximab Soravtansine (MIRV) With Carboplatin in Second-line Treatment of Folate Receptor Alpha (FRα) Expressing, Platinum-sensitive Epithelial Ovarian Cancer

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NCT05456685 · readout ≤ 102 d

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
125actual
Sites
69
Countries
Belgium, Canada, Georgia +3

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

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-09-28actualWhen the study began enrolling
Primary completionNov 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionNov 2026estimatedThe whole study's end, after follow-up
First posted2022-07-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • High Grade Ovarian Cancer
  • Primary Peritoneal Cancer
  • Fallopian Tube Cancer

Interventions

  • Drug: Mirvetuximab soravtansine — also filed as MIRV, IGN853
  • Drug: Carboplatin

Primary outcome

what the primary-completion date above is the date OF
Overall Response Rate (ORR)
measured Up to 3 years

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