drugset / Trial / NCT04625699
Study of Durvalumab + Tremelimumab in NSCLC Patients After Adjuvant Treatment
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to determine whether it is feasible and safe to give research participants investigational treatment with durvalumab and tremelimumab after they have completed standard treatment for NSCLC and once they have detectable circulating tumor DNA (ctDNA) in the blood before there is evidence of disease recurrence on imaging studies. These investigational agents are a type of immunotherapy, which is a treatment that activates your own body's immune system to treat cancer.
Timeline
- Start
- 2022-12
- Primary completion
- 2023-07
- Completion
- 2023-12
Outcome
Outcome not reported
Stopped: “Contract was never finalized.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Durvalumab | Monoclonal antibody | 1500 mg | Intravenous |
| Subject | Tremelimumab | Monoclonal antibody | 300 mg | Intravenous |