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Study of Volrustomig in Women With High Risk Locally Advanced Cervical Cancer (eVOLVE-Cervical)

← catalyst calendar

NCT06079671 · readout in 464 d

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Gynecologic Oncology Group Foundation, European Network of Gynaecological Oncological Trial Groups (ENGOT).

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
800estimated
Sites
205
Countries
Brazil, Canada, China +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
Start2023-09-22actualWhen the study began enrolling
Primary completion2027-11-26estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-09-30estimatedThe whole study's end, after follow-up
First posted2023-10-12actualWhen 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

  • Locally Advanced Cervical Cancer

Interventions

  • Biological: Volrustomig
  • Other: Placebo — also filed as Saline

Primary outcome

what the primary-completion date above is the date OF
Progression-free Survival (PFS) based on the investigator assessment in all randomized participants (FAS)
measured Up to approximately 7 years

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