πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-20

A Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirvetuximab Soravtansine in Participants With Recurrent Ovarian Cancer With High Folate Receptor-Alpha Expression (NCT06365853)

A Randomized Phase 2 Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirvetuximab Soravtansine in Patients With Recurrent Ovarian Cancer With High Folate Receptor-Alpha Expression

πŸ”΅ Active, Not Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: AbbVie

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to evaluate the incidence rate and severity of prespecified mirvetuximab soravtansine (MIRV)-related ocular treatment-emergent adverse events (TEAEs) and assess prophylaxis strategies in all participants (symptomatic and asymptomatic) undergoing prospective ophthalmic evaluation with recurrent ovarian cancer (participants with either platinum-sensitive ovarian cancer \[PSOC\] or platinum-resistant ovarian cancer \[PROC\]) with high folate receptor alpha (FRΞ±) expression.

Who can join: Review the eligibility criteria below.

Location: University of California Los Angeles /ID# 269339 β€” Los Angeles, California

Age range: 18 Years

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (41 Sites)

Showing the first 25 of 41 sites.

  • University of California Los Angeles /ID# 269339 β€” Los Angeles, California
  • UCSF Medical Center /ID# 280425 β€” San Francisco, California
  • Norton Cancer Institute - St. Matthews /ID# 269070 β€” Louisville, Kentucky
  • Holy Cross Hospital - Silver Spring /ID# 269344 β€” Silver Spring, Maryland
  • Mercy David C. Pratt Cancer Center /ID# 269350 β€” St Louis, Missouri
  • The Center Of Hope /ID# 269348 β€” Reno, Nevada
  • Holy Name Medical Center /ID# 269340 β€” Teaneck, New Jersey
  • New York Oncology Hematology - Albany Cancer Center /ID# 269345 β€” Albany, New York
  • Women'S Cancer Care Associates /ID# 269980 β€” Albany, New York
  • Duke Cancer Institute /ID# 269342 β€” Durham, North Carolina
  • Summa Health /ID# 269349 β€” Akron, Ohio
  • University of Texas - Southwestern Medical Center /ID# 269341 β€” Dallas, Texas
  • Memorial Hermann Southeast Hospital /ID# 269347 β€” Houston, Texas
  • Blacktown Hospital /ID# 269305 β€” Blacktown, New South Wales
  • Newcastle Private Hosptial /ID# 269306 β€” Lambton Heights, New South Wales
  • Monash Health - Monash Medical Centre - Clayton /ID# 269304 β€” Clayton, Victoria
  • Universitair Ziekenhuis Antwerpen /ID# 269310 β€” Edegem, Antwerpen
  • OLV Ziekenhuis Aalst /ID# 269311 β€” Aalst, Oost-Vlaanderen
  • AZ Sint-Lucas /ID# 269307 β€” Ghent, Oost-Vlaanderen
  • UZ Gent /ID# 269309 β€” Ghent, Oost-Vlaanderen
  • Universitair Ziekenhuis Leuven /ID# 269308 β€” Leuven, Vlaams-Brabant
  • CHU de Liege /ID# 269312 β€” LiΓ¨ge,
  • Universite de Montreal - Hopital Maisonneuve-Rosemont /ID# 268862 β€” Montreal, Quebec
  • Centre Hospitalier de l'Universite de Montreal /ID# 269314 β€” Montreal, Quebec
  • McGill University Health Centre - Glen Site /ID# 269313 β€” Montreal, Quebec

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—