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Impact of Circadian Rhythm on Immunotherapy

NCT07224971 PHASE2 RECRUITING

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 sponsorLiza Villaruz, MD
PhasePHASE2
StatusRECRUITING
Enrolment350
Start dateTue Dec 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionWed May 01 2030 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

United States