drugset / Trial / NCT06160531

Influenza Viral Challenge Study of CC-42344 in Healthy Participants

NCT06160531 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

Participants in this study will be given either CC-42344 (one of two dose levels) or placebo orally for 5 days after receiving an influenza (flu) challenge virus. Participants will not know whether they are getting placebo or CC-42344. The amount of virus in nasal samples will be measured over time. Side effects and pharmacokinetics (the amount of CC-42344 in blood) will also be measured.

Timeline

Start
2023-11-25
Primary completion
2024-05-03
Completion
2024-07-18

Drugs

EvaluationDrugModalityDoseRoute
Subject CC-42344 Unknown — Oral

Indications