Humanpharmakologisches Zentrum Biberach
Biberach, 88397, Germany
NCT Number: NCT05520827
Single Rising Dose (SRD) part:
The main objectives of the SRD part of this trial are to investigate safety, tolerability, and pharmacokinetics (PK) of BI 1584862 in healthy male subjects following oral administration of single rising doses.
Food Effect (FE) part:
The main objective of the FE part is to assess the influence of food on the relative bioavailability of the BI 1584862 tablet.
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Notify Me18 year–45 year
Male
Interventional
Phase 1
Biberach, 88397, Germany
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
BI 1584862
Placebo
Time frame: Up to 14 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Boehringer Ingelheim
Industry
A Randomised, Single-blind, Placebo-controlled Trial to Investigate Safety, Tolerability, and Pharmacokinetics of Single Rising Doses of BI 1584862 Administered as Tablet to Healthy Male Subjects (SRD Part), and a Randomised, Open-label, Single-dose, Two-way Crossover Part Investigating Relative Bioavailability of BI 1584862 as Tablet With and Without Food in Healthy Male Subjects (FE Part)
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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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