Study of VX-770 on Desipramine

Completed · Phase 1

Conditions studied: In Development for Cystic Fibrosis

In brief

The objective of this study is to evaluate the effects of VX-770 on Desipramine

Key facts

Study ID

NCT01153542

Run by

Vertex Pharmaceuticals Incorporated

People needed

24

Starts

2010-06-01

Expected to finish

2010-08-01

Last updated by the study team

2010-12-09

Who can join

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

You may qualify if…

• Subjects must be male or female and between 18 and 55 years of age
• Subject must have a body mass index (BMI) from 18 to 30 kg/m2
• Subject must be judged to be in good health

You may not qualify if…

• History of any illness that, in the opinion of the investigator or the subject's general practitioner, might confound the results of the study or pose an additional risk in administering study drug(s) to the subject
• Subjects who have human immunodeficiency virus, hepatitis C, or active hepatitis B
• Female subjects and male subjects with female partner(s) who are pregnant, nursing, or planning to become pregnant during the study or within 90 days of the last dose of study drug

Where it is running

• Covance CRU, Inc. — Daytona Beach, Florida, United States

Full record on ClinicalTrials.gov

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