Skip to content

A Phase III, Randomized, Open-Label, Multicenter, Global Study of Volrustomig (MEDI5752) in Combination with Carboplatin plus Pemetrexed Versus Platinum plus Pemetrexed or Nivolumab plus Ipilimumab in Participants with Unresectable Pleural Mesothelioma (eVOLVE-Meso)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-503231-17-00
Acronym
D7988C00001
Enrollment
383
Registered
2023-12-11
Start date
2024-04-26
Completion date
Unknown
Last updated
2025-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unresectable Pleural Mesothelioma

Brief summary

overall survival

Detailed description

Overall Survival and Progression Free Survival, OS and PFS at specific landmarks, Overall Response Rate, Duration of Response, and PFS2 (time from randomization to the second progression event)., TTD in physical functioning, change from baseline in disease-related symptoms, and in functioning, Incidence of ADAs against volrustomig., Concentrations of volrustomig and PK parameters as data allow, Safety and tolerability based on AEs, rates of AE-related dose discontinuations/modifications, vital signs, clinical laboratory assessments, physical examinations, and ECGs

Interventions

DRUGIPILIMUMAB
DRUGCARBOPLATIN
DRUG250 mg
DRUGPEMETREXED
DRUGNIVOLUMAB
DRUGCISPLATIN
DRUGINFLIXIMAB
DRUGvolrustomig

Sponsors

AstraZeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
overall survival

Secondary

MeasureTime frame
Overall Survival and Progression Free Survival, OS and PFS at specific landmarks, Overall Response Rate, Duration of Response, and PFS2 (time from randomization to the second progression event)., TTD in physical functioning, change from baseline in disease-related symptoms, and in functioning, Incidence of ADAs against volrustomig., Concentrations of volrustomig and PK parameters as data allow, Safety and tolerability based on AEs, rates of AE-related dose discontinuations/modifications, vital signs, clinical laboratory assessments, physical examinations, and ECGs

Countries

Belgium, Denmark, France, Germany, Italy, Netherlands, Norway, Poland, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026