Momentum Pharma Services GmbH
Hamburg, 22769, Germany
NCT Number: NCT01879020
The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of TA-8995 after multiple doses in healthy adult male subjects
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Notify Me18 year–55 year
Male
Interventional
Phase 1
Hamburg, 22769, Germany
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Drug: TA-8995 1mg
Placebo (TA-8995 1mg)
Time frame: 336 hours post dose
Time frame: 336 hours post dose
Time frame: 336 hours post dose
Time frame: 7 days post the final dose
Time frame: 7 days post the final dose
Time frame: 7 days post the final dose
Time frame: 4 hours after the first and the fibal dose
Tanabe Pharma Corporation
Industry
A Randomised Double-blind, Placebo-controlled, Ascending-dose, Phase I Study to Determine the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TA-8995 After Multiple Doses in Healthy Adult Male Subjects
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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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