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Clinical Trial ● Currently Recruiting Phase II NCT06535607

Study of Volrustomig as Monotherapy or in Combination With Anti- Cancer Agents in Participants With Advanced/Metastatic Solid Tumors

Study of Volrustomig as Monotherapy or in Combination With Anti- Cancer Agents in Participants With Advanced/Metastatic Solid Tumors — Recruiting • Phase II • Oncology • NCT06535607.

📅 26 May 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06535607
Sponsor
AstraZeneca
Start
2024-08-22
ClinicaliQ Trial Snapshot
  • Study of Volrustomig as Monotherapy or in Combination With Anti- Cancer Agents in Participants With Advanced/Metastatic Solid Tumors — Recruiting • Phase II • Oncology • NCT06535607.
  • What is being tested: Volrustomig, a novel anti-cancer agent, is being evaluated both as a standalone treatment and combined with existing anti-cancer drugs in patients with advanced or metastatic solid tumors.
  • Patient eligibility overview: The trial enrolls patients diagnosed with advanced or metastatic solid malignancies who meet specific disease stage criteria; detailed inclusion/exclusion criteria determine suitability for monotherapy versus combination treatment arms.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

eVOLVE-02 study will evaluate the efficacy and safety of volrustomig as monotherapy or in combination with anti-cancer agents in participants with advanced/metastatic solid tumors.

Eligibility Snapshot
  • : * Age ≥18 at the time of signing the ICF. * Provision of tumor sample to assess the PD-L1 expression (if applicable). * ECOG performance status of 0 or 1. * Measurable disease according to RECIST 1.1 (variations of RECIST 1.1 if applicable). * Life expectancy ≥ 12 weeks. * Adequate organ and bone marrow function. * Body weight > 35 kg * Capable of giving signed informed consent.

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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