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Active, not recruiting Phase 1

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 · tracked via the Priya Life Science Japan tracker
Phase
Phase 1
Started
2026-07-21
Last updated
2026-10-01

Condition(s) studied

HealthyObesity

Investigational drug(s) / intervention(s)

BI 3034701 →Placebo

BI 3034701: BI 3034701

Placebo: Placebo

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
64 Years
Healthy volunteers
Accepted
Inclusion criteria : 1. Japanese ethnicity, according to the following criteria: born in Japan, have lived outside of Japan \< 10 years, and have parents and grandparents who are Japanese 2. Part 1: Male or female trial participants according to the assessment of the investigator, as based on a complete medical history including a physical examination, vital signs (blood pressure, pulse rate), 12-lead electrocardiogram, and clinical laboratory tests 3. Part 2: Healthy male or female trial participants according to the assessment of the investigator, as based on a complete medical history including a physical examination, vital signs (blood pressure, pulse rate), 12-lead electrocardiogram, and clinical laboratory tests 4. Parts 1 and 2: Age of 18 to 64 years (inclusive) 5. Further inclusion criteria apply. Exclusion criteria : 1. Any finding in the medical examination (including blood pressure, pulse rate or electrocardiogram) deviating from normal and assessed as clinically relevant by the investigator 2. Repeated measurement of systolic blood pressure outside the range of 90 to 140 mmHg, diastolic blood pressure outside the range of 50 to 90 mmHg, or pulse rate outside the range of 50 to 90 beats per minute 3. Any laboratory value outside the reference range that the investigator considers to be of clinical relevance and, in particular: alanine aminotransferase (ALT) above upper limit of normal (ULN) + 20%, aspartate aminotransferase (AST) above ULN + 20%, gamma-glutamyl transferase (GGT) above ULN + 20%, Lipase or amylase above ULN + 20%, bilirubin above 1.2x ULN (except for cases of Gilbert's Syndrome), estimated glomerular filtration rate (eGFR) \< 80 mL/min/1.73 m² 4. Part 1: Body weight increase or decrease (self-reported) of greater than 5% in the 3 months prior to screening 5. Further exclusion criteria apply.

Primary outcome measure(s)

  • Occurrence of any treatment-emergent adverse event assessed as drug-related by the investigator — Part 1: up to Week 19, Part 2: up to Week 10
    Expressed as the percentage of trial participants treated with investigational drug who experience such an event

Trial sites (3)

FacilityCityRegionStatus
SOUSEIKAI Hakata Clinic Fukuoka, Fukuoka Japan
Fukuoka Mirai Hospital Fukuoka, Fukuoka Japan
SOUSEIKAI Sumida Hospital Tokyo, Sumida-ku Japan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07693231 on ClinicalTrials.gov ↗ ← All trials in Japan