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NCT06097728 · ClinicalTrials.gov registry record · Phase 3
MEDI5752 in Combination With Carboplatin Plus Pemetrexed in Unresectable Pleural Mesothelioma
A Phase 3 study of Unresectable Pleural Mesothelioma, sponsored by AstraZeneca.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 825
- Enrollment target
- 20
- Study locations
NCT06097728 is a Phase 3 study of Unresectable Pleural Mesothelioma that is actively recruiting participants, run by AstraZeneca. The registered enrollment target is 825 participants. The trial reports 20 study locations across 13 states.
The verdict
NCT06097728, a Phase 3 study of Unresectable Pleural Mesothelioma, is actively recruiting participants, sponsored by AstraZeneca.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 825 participants
- Enrollment target
- 20
- Study locations
Study Summary
This is a phase III, randomized, open-label, multicenter, global study to determine the efficacy and safety of Volrustomig (MEDI5752) + Carboplatin + Pemetrexed vs the investigator's choice of platinum + Pemetrexed or Nivolumab + Ipilimumab in participants with unresectable pleural mesothelioma.
Conditions Studied
Interventions
- DRUG Carboplatin
- DRUG Cisplatin
- DRUG Pemetrexed
- DRUG Nivolumab
- DRUG Volrustomig
Study Locations (20)
Ohio
- Research Site - Cleveland
- Research Site - Cleveland
- Research Site - Cleveland
- Research Site - Columbus
- Research Site - Independence
California
- Research Site - Duarte
- Research Site - Santa Rosa
New York
- Research Site - Commack
- Research Site - Valhalla
Oregon
- Research Site - Portland
- Research Site - Portland
Arizona
- Research Site - Phoenix
Colorado
- Research Site - Aurora
Florida
- Research Site - Jacksonville
Georgia
- Research Site - Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 825 participants |
| Start Date | 2023-11-09 |
| Est. Completion | 2028-11-16 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06097728
The ClinicalTrials.gov registry entry for NCT06097728 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 825 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Unresectable Pleural Mesothelioma appearing as the primary indexed condition, and to 5 interventions - of which Carboplatin is the first listed.
NCT06097728 reports 20 study locations spanning 13 distinct geographic areas - top geographies include Ohio, California, New York.
Frequently Asked Questions
What is clinical trial NCT06097728 about?
NCT06097728 is a clinical study titled "MEDI5752 in Combination With Carboplatin Plus Pemetrexed in Unresectable Pleural Mesothelioma". This is a phase III, randomized, open-label, multicenter, global study to determine the efficacy and safety of Volrustomig (MEDI5752) + Carboplatin + Pemetrexed vs the investigator's choice of platinum + Pemetrexed or Nivolumab + Ipilimumab in participants with unresectable pleural mesothelioma.
What is the current status of trial NCT06097728?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 825 participants. The study started on 2023-11-09. Estimated completion is 2028-11-16.
What conditions does trial NCT06097728 study?
This clinical trial studies the following conditions: Unresectable Pleural Mesothelioma.
What interventions are being tested in trial NCT06097728?
The interventions under investigation include: Carboplatin (DRUG), Cisplatin (DRUG), Pemetrexed (DRUG), Nivolumab (DRUG), Volrustomig (DRUG).
Who is sponsoring clinical trial NCT06097728?
This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06097728 being conducted?
This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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