Vince and Associates
Overland Park, Kansas, 66212, United States
NCT Number: NCT03203499
This is a single-center, randomized, double-blind, placebo-controlled, single-ascending-dose study to evaluate the safety and tolerability of the coadministration of up to 6 dose levels of ANS-6637 and EtOH in healthy male moderate alcohol drinkers. The study will include a screening visit, a qualification visit, a Treatment Phase and follow-up.
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Notify Me21 year–45 year
Male
Interventional
Phase 1
Overland Park, Kansas, 66212, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ascending single doses administered orally.
Placebo administered orally.
Time frame: Up to 36 hours postdose
Time frame: Up to 48 hours postdose
Time frame: Up to 48 hours postdose
Time frame: Up to 48 hours postdose
Time frame: Up to 6 hours postdose
Time frame: Up to 6 hours postdose
Amygdala Neurosciences, Inc.
Industry
A Phase 1b, Proof of Concept, Dose-Ranging Study to Evaluate the Safety of the Coadministration of Ascending Doses of ANS-6637 and Ethanol in Healthy Male Moderate Drinkers
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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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