drugset / Trial / NCT03918252
Neoadjuvant Immune Checkpoint Blockade in Resectable Malignant Pleural Mesothelioma
Phase 2
Active not recruiting
30 enrolled
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Bristol-Myers Squibb · collab
Non-randomizedSequentialOpen-labelTreatment
Summary
The proposed study will evaluate the safety and feasibility of neoadjuvant nivolumab +/- ipilimumab in resectable MPM. In addition, maintenance nivolumab will be administered for 1 year following completion of standard bi-/tri-modality therapy.
Timeline
- Start
- 2019-10-02
- Primary completion
- 2027-06
- Completion
- 2028-06
Publications
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Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ipilimumab | Monoclonal antibody | 1 mg/kg | Intravenous |
| Subject | Nivolumab | Monoclonal antibody | 3 mg/kg | Intravenous |
| Subject | Nivolumab | Monoclonal antibody | 240 mg | Intravenous |