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Impact of Circadian Rhythm on Immunotherapy
This study aims to determine whether morning versus afternoon treatment impacts efficacy of (standard of care) immunotherapy in a broad patient population. Patients with any type of advanced/metastatic malignancy are eligible to enroll in this study, as long as first-line anti-PD-1/PD-L1 immunotherapy is on label for their condition. Participants will then be randomized to either the early treatment group (administration must start and conclude by 11:00 AM +1 hour window) or the late treatment group (administration must start after 12:00 PM).
Details
| Lead sponsor | Liza Villaruz, MD |
|---|---|
| Phase | PHASE2 |
| Status | RECRUITING |
| Enrolment | 350 |
| Start date | Tue Dec 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Wed May 01 2030 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Advanced/Metastatic NSCLC
Interventions
- Immunotherapy - PD-1 Blocker
Countries
United States