drugset / Trial / NCT07693231

A Study to Test How Well Different Doses of BI 3034701 Are Tolerated by Japanese Healthy People and Japanese People With Obesity or Overweight

NCT07693231 ↗

Phase 1 Not yet recruiting 48 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

Part 1: To investigate safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of BI 3034701 in Japanese male and female participants with body mass index (BMI) ≥27.0 kg/m² or more following subcutaneous administration of multiple rising doses over 16 weeks. Part 2: To investigate safety, tolerability, and PK of BI 3034701 in Japanese male and female healthy participants with BMI ≥23.0 to \<27.0 kg/m² following subcutaneous administration of multiple rising doses over 7 weeks.

Timeline

Start
2026-07-21
Primary completion
2026-12-22
Completion
2027-01-05

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 3034701 Unknown — Subcutaneous

Indications