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A Study of XmAb20717 (Vudalimab)in Patients With Selected Advanced Gynecologic and Genitourinary Malignancies

← catalyst calendar

NCT05032040

Sponsored by Xencor, Inc. (industry) · XNCR — their whole pipeline →. With ICON plc.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
170estimated
Sites
17
Country
United States

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
Start2022-07-21actualWhen the study began enrolling
Primary completion2025-10-15estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-12-30estimatedThe whole study's end, after follow-up
First posted2021-09-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-02-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Ovarian Cancer
  • Clear Cell Carcinoma
  • Endometrial Cancer
  • Cervical Carcinoma
  • Metastatic Castration-Resistant Prostate Cancer (mCRPC)

Intervention

  • Biological: vudalimab

Primary outcome

what the primary-completion date above is the date OF
PSA50 is the primary endpoint for the mCRPC cohort. Objective Response Rate (ORR) as assessed by Response Evaluation Criteria in Solid Tumours (RECIST) version 1 criteria is the primary endpoint for gynecological malignancy cohorts
measured 12 weeks

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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