A Study to Investigate the Safety, Tolerability and Pharmacokinetics of SUVN-G3031 in Healthy Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Cognitive Disorders
In brief
The purpose of this study is to investigate the safety, tolerability and pharmacokinetics of SUVN-G3031 in healthy male subjects following single or multiple ascending doses.
Key facts
- Study ID
- NCT02342041
- Run by
- Suven Life Sciences Limited
- People needed
- 64
- Starts
- 2014-09-01
- Expected to finish
- 2015-08-01
- Last updated by the study team
- 2016-10-14
Who can join
Age: 18 and older, up to 45. Sex: male. Healthy volunteers: accepted.
You may qualify if…
- Healthy male aged 18 to 45 years with a BMI between 18 and 30 kg/m2, (inclusive).
You may not qualify if…
- Standard exclusion criterion for Phase 1 clinical trial in healthy subjects.
- History of any clinically significant disease or disorder which, in the opinion of the Investigator, may either put the volunteer at risk because of participation in the study, or influence the results or the volunteer's ability to participate
- History or presence of GI, hepatic, or renal disease or any other condition known to interfere with absorption, distribution, metabolism, or excretion of drugs as judged by Investigator.
Where it is running
- Quintiles — Overland Park, Kansas, United States
Full record on ClinicalTrials.gov
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