drugset / Trial / NCT05738850

Study to Assess Adverse Events and How ABBV-932 Oral Capsules Moves Through the Body of Healthy Adult Participants

NCT05738850 ↗

Phase 1 Completed 104 enrolled AbbVie Gedeon Richter Ltd. · collab
RandomizedSequentialQuadruple-blindTreatment

Summary

The main objective of this study is to assess pharmacokinetics, safety, and tolerability of ABBV-932 in healthy adult participants.

Timeline

Start
2023-02-15
Primary completion
2024-05-31
Completion
2024-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-932 Unknown — Oral