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Study details
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A Study Comparing Sacituzumab Tirumotecan to Other Treatments for Recurrent Cervical Cancer

Merck Sharp & Dohme LLC
NCT IDNCT06459180ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

686

Study length

about 3.9 years

Ages

18+

Sex

Female only

Locations

38 sites in AK, AL, AZ +17

What this study is about

This trial is testing sacituzumab tirumotecan, a new treatment, against other treatments (Treatment of Physician's Choice or TPC) as a second-line treatment for people with recurrent or metastatic cervical cancer. The goal is to see if sacituzumab tirumotecan helps patients live longer and has fewer side effects compared to the other treatments.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Sacituzumab Tirumotecan
  • 2.Receive Tisotumab Vedotin
  • 3.Take Gemcitabine
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

gemcitabine, irinotecan, pemetrexed, tisotumab vedotin, topotecan, vinorelbine

Drug routes

injection (Injection), oral (Oral Capsule)

Endpoints

Primary: Number of Participants Discontinuing Study Treatment Due to an AE in Sacituzumab Tirumotecan Run-in, Number of Participants Experiencing One or More Adverse Events (AEs) in Sacituzumab Tirumotecan Run-in, Objective Response Rate (ORR) in Sacituzumab Tirumotecan Run-in, Overall Survival (OS) in Phase 3 Portion

Secondary: Change from Baseline in EORTC QLQ-C30 Global Health Status (Item 29) and Quality of Life (Item 30) Combined Score in Phase 3 Portion, Change from Baseline in EORTC QLQ-C30 Physical Functioning Score in Phase 3 Portion, Change from Baseline in EORTC QLQ-C30 Role Functioning Score in Phase 3 Portion, Duration of Response (DOR) in Phase 3 Portion, Number of Participants Discontinuing Study Treatment Due to an AE in Phase 3 Portion, Number of Participants Experiencing One or More AEs in Phase 3 Portion, ORR in Phase 3 Portion, Progression-free Survival (PFS) in Phase 3 Portion

Body systems

Oncology