HPTN 083-01

Safety, Tolerability and Acceptability of Long-Acting Cabotegravir (CAB LA) for the Prevention of HIV among Adolescent Males – A sub-study of HPTN 083

Study Summary
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Study Documents - Study Details - Key Study Personnel - Study Sites - Publications

 

 Visit the HPTN 083-01 Website 

What is HPTN 083-01?

HPTN 083-01 is a clinical trial examining whether injectable cabotegravir (CAB) for PrEP (pre-exposure prophylaxis) is safe and acceptable for adolescent males [assigned male at birth – including men who have sex with men (MSM), transgender women (TGW), and gender nonconforming people].

Who is participating in HPTN 083-01?

This study will be enrolling about 50 adolescent males (assigned male at birth – including MSM, TGW, and gender nonconforming people) under the age of 18 at sites in Boston, Chicago, and Memphis. 

Why is HPTN 083-01 important?

Adolescents and young adults make up a large number of new HIV infections worldwide. Although taking a daily pill for PrEP works to protect people from HIV, having to take a daily pill has proven to be difficult for some people. Long-acting injectable PrEP has the potential to protect people from HIV without having to take a daily pill.

What will happen during HPTN 083-01?

Participants will move through the study in 3 steps:

Step 1: Participants will take one CAB pill every day for five weeks

Step 2: Participants will receive a total of 5 CAB injections over 6 months

Step 3: Participants will come to the clinic for study visits quarterly and receive Truvada for PrEP for about one year.

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Study Documents

Version 3.0

Version 2.0

Version 1.0

➤ HPTN 083-01 SSP

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Previous versions of the SSP sections are available upon request
 

HPTN 083-01 Study-Specific Procedures Summary of Changes - 8 December 2022

Cover Page

Section 1: Introduction

Section 2: Protocol

Section 3: Document Requirements

Section 4: Recruitment, Screening, and Enrollment

Section 5: Study Procedures Overview

Section 6: Visit Checklists

Section 7: Participant Retention

Section 8: Study Product Considerations

Section 9: Clinical Considerations

Section 10: Adverse Event Reporting and Safety Monitoring

Section 11: Laboratory and Specimen Management Procedures

Section 12: Counseling Considerations

Section 13: Data Management

Section 14: Computer Assisted Self-Interview (CASI)

Section 15: Reporting Plan

Section 16: Data Communiqués

Section 17: Qualitative

Appendix 1A: Record of Dispensation of Participant-Specific Study Product to Non-Pharmacy Staff

Appendix 1B: Record of Product Return of Participant-Specific Study Product by Non-Pharmacy Staff

Appendix II: Participant Transfer and Receipt Process within Medidata Rave

Appendix III: Guidance for the Management of “Discordant/discrepant” HIV Testing Results

Appendix IV: Study Schema

Other tools

 

Presentations

Engaging Adolescent Sexual and Gender Minority Persons in Long-Acting HIV Pre-Exposure Prophylaxis in the U.S.

Douglas Krakower | International Workshop on HIV & Pediatrics 2022 | 27 July 2022

 

More Study Documents

You must request access to private documents (i.e. call summaries) from the study team. Please email Gabriela Salinas-Jimenez at GSalinas-Jimenez@fhi360.org for access to these documents.

Study Details

Protocol Status: Closed to Follow Up
Study Purpose:

To establish the minimum safety, tolerability and acceptability data needed to support the use of cabotegravir long-acting injection (CAB LA) in an adolescent population, potentially transforming the field of HIV prevention for young people.

Study Design:

A Phase IIB single arm, open label safety, tolerability, and acceptability study

Study Population:

Sexually-active, healthy male (assigned at birth) adolescents aged below 18 years

Study Size:

Approximately 50

Study Duration:

Participant recruitment will take approximately 12 months. Oral study product will be administered for 5 weeks, followed by 29 weeks on injectable product, then quarterly visits for 48 weeks after final injection. All participants who have received at least one injection will be followed for 48 weeks after their last injection. Waning levels of cabotegravir (the PK tail) will be covered with locally sourced oral TDF/FTC for daily use for 48 weeks. Total study duration per participant will be approximately 21 months.

Treatment Regimen:

Step 1 – oral cabotegravir (30mg tablet); Step 2 – 3 mL (600 mg) intramuscular (IM) injection; Step 3 – Tenofovir/Emtricitabine (Trade name: TDF/FTC, Truvada®) (300mg/200mg tablet)

Primary Objectives:

• To evaluate the safety, tolerability and acceptability of CAB LA in healthy HIV-uninfected male adolescents aged below 18 years

Secondary Objectives:

• To examine adherence to and timeliness of injections over time among adolescent participants who are provided CAB LA and information regarding its safety and unknown efficacy.
• To examine patterns of sexual risk behavior over time among adolescent participants who are provided CAB LA and information regarding its safety and unknown efficacy.
• To evaluate the safety of CAB LA for 48 weeks of follow-up after final injection.
• To characterize the pharmacokinetics of CAB LA.

Key Study Personnel

Adeola Adeyeye, DAIDS Medical Officer
erica hamilton, LOC Clinical Research Manager
Sybil Hosek, Protocol Chair
Bill Kapogiannis, NICHD Medical Officer
Scott Rose, LOC Clinical Research Manager
Lynda Stranix-Chibanda, Protocol Co-Chair