PRA Health Sciences
Groningen, 9728 NZ, Netherlands
NCT Number: NCT03725072
The purpose of the study is to determine the absorption, metabolism, and excretion of [14C]-evobrutinib in healthy participants
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Notify Me18 year–55 year
Male
Interventional
Phase 1
Groningen, 9728 NZ, Netherlands
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive a single, oral dose of evobrutinib under fasting conditions as a solution, which will contain [14C]-evobrutinib.
Other names: M2951
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: Pre-dose up to Day 35 post-dose
Time frame: From time of first dose to end of study participation approximately at Day 37
Number of participants with clinically significant abnormalities will be reported.
Time frame: From time of first dose to end of study participation approximately at Day 37
Time frame: From time of first dose to end of study participation approximately at Day 37
Merck KGaA, Darmstadt, Germany
Industry
Phase I, Open Label, Single Dose Study to Determine the Pharmacokinetics, Metabolism, and Excretion of [14C]-Evobrutinib in Healthy Participants
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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