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NCT05518708

A Study in Healthy Men to Test How Different Doses of BI 3032950 Are Tolerated

Completed Phase 1 Last updated 26 September 2023
What this trial tests

Phase 1 trial testing BI 3032950 in Healthy in 94 participants. Completed in 21 September 2023.

Timeline
27 September 2022
Primary endpoint
21 September 2023
21 September 2023

Quick facts

Lead sponsorBoehringer Ingelheim
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment94
Start date27 September 2022
Primary completion21 September 2023
Estimated completion21 September 2023
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Boehringer Ingelheim — full company profile →

Who can join

Adults 18 to 65, male only, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main objectives of this trial are to investigate safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of BI 3032950 in healthy male subjects following intravenous (Part A) or subcutaneous (Part B) administration of single rising doses.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of BI 3032950

Trials testing the same drug.

Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Boehringer Ingelheim trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05518708.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing