1307.1.1 Boehringer Ingelheim Investigational Site
Neuss, Germany
NCT Number: NCT01587417
To investigate safety, tolerability, pharmacokinetics including dose proportionality, and pharmacodynamics of BI 187004 CL within a predefined dose range
Looking for future studies?
Notify Me18 year–55 year
Male
Interventional
Phase 1
Neuss, Germany
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1 single dose per subject as oral solution
1 single dose per subject as oral solution
Time frame: up to 15 days postdose
Time frame: up to 96 hours postdose
Time frame: up to 96 hours postdose
Time frame: up to 96 hours postdose
Boehringer Ingelheim
Industry
A Randomised, Double-blind, Placebo-controlled Trial in Healthy Volunteers to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Oral Doses of 2.5 mg to 360 mg of BI 187004 CL
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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