drugset / Trial / NCT06531811

A Study to Investigate the Relative Bioavailability of AZD8630 Following a Device and Formulation Transition in Healthy Participants.

NCT06531811 ↗

Phase 1 Completed 32 enrolled AstraZeneca
RandomizedCrossoverOpen-labelOther

Summary

The purpose of this study is to evaluate the potential difference between pharmacokinetics (PK), safety, tolerability and device performance between the AZD8630 test formulation and the AZD8630 reference formulation.

Timeline

Start
2024-08-06
Primary completion
2024-10-03
Completion
2024-10-03

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD8630 Unknown — Inhaled

Indications

No indication recorded.