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Study of Sacituzumab Govitecan Versus Treatment of Physician's Choice in Participants With Endometrial Cancer After Platinum-Based Chemotherapy and Immunotherapy (ASCENT-GYN-01/GOG-3104/ENGOT-en26)

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NCT06486441 · readout ≤ 1,046 d

Sponsored by Gilead Sciences (industry) · GILD — their whole pipeline →. With GOG Foundation, European Network of Gynaecological Oncological Trial Groups (ENGOT), Asia-Pacific Gynecologic Oncology Trials Group.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
640estimated
Sites
189
Countries
Australia, Brazil, Canada +16

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
Start2024-08-28actualWhen the study began enrolling
Primary completionJun 2029estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJun 2029estimatedThe whole study's end, after follow-up
First posted2024-07-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Endometrial Cancer

Interventions

  • Drug: Sacituzumab govitecan-hziy — also filed as Trodelvy™, GS-0132
  • Drug: Doxorubicin — also filed as Adriamycin
  • Drug: Paclitaxel — also filed as Taxol

Primary outcomes

what the primary-completion date above is the date OF
Progression-Free Survival (PFS) As Assessed by Blinded Independent Central Review (BICR)
measured Up to approximately 27 months
Overall Survival (OS)
measured Up to approximately 47 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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