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A Phase III Study to Evaluate Long-Acting Antiretroviral Therapy in Non-adherent HIV-Infected Individuals (The LATITUDE Study)

Clinical Trial Details

This study is being conducted to test if injectable, long-acting anti-HIV drugs that are given every month can be used safely and effectively in individuals who are infected with HIV and who have had problems taking daily medications in the past. This study is also being conducted to evaluate how well are these study drugs tolerated.
   
The drugs being looked at in this study are oral cabotegravir, oral rilpivirine, long-acting injectable cabotegravir and long-acting injectable rilpivirine. A long-acting drug means it stays in the body much longer compared to the usual form of the drugs. Only oral rilpivirine is currently approved by the U.S. Food and Drug Administration (FDA) for treating HIV/AIDS in individuals who have never taken antiretroviral (ARV) drugs. Oral cabotegravir, long-acting cabotegravir and long-acting rilpivirine are experimental drugs.

Key Eligibility: 
  • people living with HIV, who have had problems taking daily medications in the past
  • age 18 years or older

    Detailed eligibility will be reviewed when you contact the study team

Study contact by location

Upper East Side - Manhattan

Contact(s)

Rebecca Fry, NP
212-746-7204
ref2007@med.cornell.edu

Chelsea - Manhattan

Chelsea Clinical Trial Location

Contact(s)

Shaun Barcavage, NP
212-746-7204
srb4001@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

2012023041

ClinicalTrials.gov:

NCT03635788

Sponsor:

A5359

Status

Open to Enrollment

Age Group

Adult

Sponsor