Study identifier:D6960C00005
ClinicalTrials.gov identifier:NCT07652658
EudraCT identifier:N/A
CTIS identifier:2025-525016-41-00
A Phase IIb Study to Evaluate the Efficacy, Safety, and Tolerability of AZD8965 in Participants with Idiopathic Pulmonary Fibrosis (IPF) (ARGiNAUT)
Idiopathic Pulmonary Fibrosis (IPF)
Phase 2
No
AZD8965 low dose, AZD8965 medium dose, AZD8965 high dose
All
359
Interventional
40 Years - n/a
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Jun 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Placebo Comparator: Placebo for AZD8965 Placebo for AZD8965 | Other: Placebo for AZD8965 Placebo for AZD8965 |
| Experimental: AZD8965 low dose AZD8965 low dose | Drug: AZD8965 low dose AZD8965 low dose |
| Experimental: AZD8965 medium dose AZD8965 medium dose | Drug: AZD8965 medium dose AZD8965 medium dose |
| Experimental: AZD8965 high dose AZD8965 high dose | Drug: AZD8965 high dose AZD8965 high dose |