Study to Assess the Safety and Pharmacokinetic (PK) of CTP-692 in Healthy Volunteers

Completed · Phase 1 · Has a placebo group

Conditions studied: Healthy

In brief

This study will assess the safety and pharmacokinetic (PK) profile of single ascending doses of CTP-692 in healthy volunteers.

Key facts

Study ID

NCT03830463

Run by

Concert Pharmaceuticals

People needed

42

Starts

2019-01-24

Expected to finish

2019-03-28

Last updated by the study team

2019-06-13

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy adult males and females between 18 and 55 years of age, inclusive
• Body weight ≥ 55 kg and BMI within the range of 18 to 32 kg/m2, inclusive

You may not qualify if…

• Screening laboratory measurements outside the normal range associated with potential risk for the treatment under investigation at screening and/or prior to the first dose of study drug
• Positive blood screen for human immunodeficiency virus (HIV antibody), hepatitis B virus surface antigen or hepatitis C virus antibody
• History of clinically significant central nervous system (e.g., seizures), cardiac, pulmonary, metabolic, renal, hepatic or gastrointestinal (GI) conditions
• Positive drug or alcohol test at screening or prior to the first dose of study drug

Where it is running

• Collaborative Neuroscience Network, LLC — Long Beach, California, United States

Full record on ClinicalTrials.gov

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