ACTIVE_NOT_RECRUITING

Cisgender Female Patients Who Start on Long Acting Cabotegravir for PrEP

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Oral PrEP regimens (FTC/TDF have been the mainstay of HIV prevention however patients now have more options for HIV prevention. In addition to oral PrEP regimens, the FDA approved the use of long acting Cabotegravir (CAB-LA) as the first long-acting medication for HIV prevention. This study will evaluate real world clinical outcomes of cisgender female patients who start CAB-LA for PrEP.

Official Title

Real World Clinical Outcomes in Cisgender Female Patients Who Start on Long Acting Cabotegravir for PrEP: An Observational, Multisite Prospective 2 Year Study in the Southern U.S.

Quick Facts

Study Start:2024-01-02
Study Completion:2027-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06145854

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Cisgender females, ages 18 years and older
  2. 2. Negative HIV test at baseline
  3. 3. Negative Pregnancy test at baseline
  4. 4. Weigh at least 35 kilograms
  5. 5. Already Prescribed CAB-LA (Apretude)
  1. 1. Transgender females or males
  2. 2. Cisgender males
  3. 3. Cisgender female who is actively breastfeeding
  4. 4. Severe hepatotoxicity
  5. 5. Evidence of Hepatitis B Infection
  6. 6. History or presence of allergies to cabotegravir or its components

Contacts and Locations

Study Locations (Sites)

Midway Specialty Care Center
Orlando, Florida, 32819
United States
Midway Specialty Care Center
Temple Terrace, Florida, 33617
United States
Midway Specialty Care Center
West Palm Beach, Florida, 33401
United States

Collaborators and Investigators

Sponsor: Midway Specialty Care Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-02
Study Completion Date2027-03-31

Study Record Updates

Study Start Date2024-01-02
Study Completion Date2027-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • Hiv