LivingGLP1
Study S000040

A Phase I, Single-blinded, Randomized, Multiple Dose, Placebo-controlled Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Different Dose Escalation Schemes of BI 456906 in Healthy Japanese Male Subject With BMI 23-40 kg/m2

Registration

Registration
NCT04384081
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
SINGLE
Status
COMPLETED
Enrollment
37
Start
2020-06-01
Primary completion
2020-11-17
Lead sponsor
Boehringer Ingelheim
Conditions
Healthy
Interventions
DRUG:BI 456906; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Cumulative percentage (%) of subjects withdrawn from up-titration by dose escalation scheme. [up to 113 days]

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