Evaluating the Safety, Pharmacokinetics, and Antiviral Activity of a Human Monoclonal Antibody (VRC01) in HIV-Infected Adults Undergoing a Brief Treatment Interruption
Completed · Phase 1
Conditions studied: HIV Infections
In brief
The purpose of this study was to evaluate the safety, tolerability, pharmacokinetics (PK), and antiviral activity of an antibody (called VRC01) in HIV-infected adults whose HIV was well-controlled with HIV medicines. The study examined whether VRC01 controlled or delayed the return of HIV viremia when the participants' HIV medicines were briefly stopped during the study.
Key facts
- Study ID
- NCT02463227
- Run by
- National Institute of Allergy and Infectious Diseases (NIAID)
- People needed
- 14
- Starts
- 2015-08-01
- Expected to finish
- 2016-10-01
- Last updated by the study team
- 2021-10-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Alabama CRS — Birmingham, Alabama, United States
- Penn Therapeutics, CRS — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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