← Eichor
Study identifier: NCT05243524 Synced from ClinicalTrials.gov · July 28, 2026
● Terminated

Maveropepimut-S (MVP-S) and Low-Dose CPA in Patients With Platinum-Resistant Ovarian Cancer

Condition: Platinum-resistant Epithelial Ovarian Cancer  ·  Sponsor: ImmunoVaccine Technologies, Inc. (IMV Inc.)

PhasePhase 2
Planned participants16
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Phase 2, single arm, study to assess the efficacy and safety of maveropepimut-S (MVP-S) and low-dose cyclophosphamide (CPA) in subjects with recurrent, platinum resistant ovarian cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (6)

Stanford Health CarePalo Alto, California, United States
Ocala OncologyOcala, Florida, United States
NYU Langone Hospital-Long IslandMineola, New York, United States
NYU Langone: Laura and Isaac Perlmutter Cancer CenterNew York, New York, United States
CHUM - Centre hospitalier de l'Université de MontréalMontreal, Quebec, Canada
PanOncology TrialsSan Juan, Puerto Rico

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05243524