Estradiol Therapy In Transgender Women to Research Interactions With HIV Therapy (GET IT RIgHT)

Giving Standardized Estradiol Therapy In Transgender Women to Research Interactions With HIV Therapy

Transgender women (TW) are a key population and priority for HIV treatment. More research is needed to develop evidence-based clinical guidance when it comes to choosing antiretroviral treatment (ART) regimens for TW on feminizing hormonal therapy (FHT). Concerns about ART interacting with FHT and decreasing its effectiveness can lead to decreased ART adherence and increased viral loads.

The GET IT RiGHT trial aims to address concerns about drug-drug interactions (DDIs) between ART and FHT while providing access to hormonal therapy to TW living with HIV. Data suggest that access to FHT improves adherence to HIV treatment and decreases treatment interruptions.

This is an open-label, non-randomized, 3-group trial of adult TW and other individuals identifying as female or transfeminine but with male sex assigned at birth living with HIV. Participants will be on ART at entry and receive study-supplied 17-β estradiol for FHT for 48 weeks.

The primary objectives of the study are to 1) assess whether TW continue to achieve therapeutic concentrations of ART while receiving FHT for 48 weeks and 2) assess whether serum estradiol concentrations on FHT (across a range of estradiol doses) vary between boosted and un-boosted ART regimens.

Study Overview

• Status: Recruiting
• Conditions: HIV I Infection
• Intervention / Treatment: Drug: Estradiol

Detailed Description

A5403 is a phase IIb, 48-week, open-label, non-randomized, 3-group trial, of 90 adult (≥18 years) transgender women and other individuals identifying as female or transfeminine but with male sex assigned at birth (TW) living with HIV on suppressive antiretroviral therapy (ART) and not currently on FHT. The trial will target at least 50% enrollment of participants identifying as non-white or Latine.

The trial consists of three groups, a BIC-treated group (BIC/TAF/FTC; n=30) (Group 1), a DTG-treated group (DTG/TDF/FTC or 3TC; n=30) (Group 2), and a boosted DRV-treated group (DRV/c; n=30) (Group 3), for a total of 90 participants.

All participants will continue on ART (not provided by the trial) and receive study-supplied 17-β estradiol for weeks 0-48. At entry, participants will be assigned to one of the three analysis groups based on their current ART regimen. Participants on other ART regimens at screening who are willing to switch to one of the regimens above, may also be enrolled.

All participants will receive study supplied 17-β estradiol for weeks 0-48. Oral 17-β estradiol 2 mg once daily will be initiated at study entry. At weeks 4, 12, 24, and 36, study clinicians may titrate 17-β estradiol in 2 mg increments as described in the protocol.

Intensive PK subgroup (n=15 per ART group): At entry (week 0), an 8-hour intensive PK sampling will assess ART exposure prior to FHT initiation. At week 24, intensive sampling will be repeated to assess 17-β estradiol and ART exposure. A final intensive PK visit will occur at week 48 to assess 17-β estradiol and ART exposure at the maximal FHT dosing achieved during the study period.

Sparse PK sampling: all participants not participating in an intensive PK sampling visit on the same day will have timed, sparse PK sampling collected at each visit to characterize the trough plasma (BIC, DTG, and DRV) and intracellular ART (TFV-DP, FTC-TP, 3TC-TP) concentrations to evaluate the relationship of ART PK exposure across a range of 17-β estradiol doses.

FHT satisfaction and acceptability:

To measure acceptability, participants will be asked to self-report the degree to which they find the intervention appropriate and useful using Likert-type agreement scales at three study time points: entry, 24 weeks, and 48 weeks. To measure satisfaction, the 12-question Transgender Congruence Scale (TCS) will be used, which will assess associations between gender-affirming treatments, perceived gender congruence, and satisfaction at three study time points: entry, 24 weeks, and 48 weeks. In addition, brief, 20-minute, semi-structured interviews will be conducted with 30 purposively sampled participants across English- or Spanish-speaking sites to provide an opportunity for more in-depth (open-ended) feedback on intervention satisfaction and acceptability at three time points: entry, 24 weeks, and 48 weeks.

Other assessments throughout the study include: anthropometric measurements (including weight, height, minimum waist circumference, and maximum hip circumference), routine chemistry and hematology labs, HIV-1 RNA, CD4+ and CD8+ T cell counts and percentages, lipids, glucose and insulin, non-estradiol hormone concentrations, stored PBMC, plasma, and serum, and ART and FHT adherence assessments.

• Study Type: Interventional
• Enrollment (Estimated): 90
• Phase: Phase 2

Contacts and Locations

Study Locations

• Botswana
  • Gaborone, Botswana
    • Not yet recruiting
    • Gaborone CRS (12701)
    • Contact: Unoda A Chakalisa; Phone Number: 267-393-1353; Email: uchakalisa@bhp.org.bw
• Brazil
  • Porto Alegre, Brazil, 91350-200
    • Not yet recruiting
    • Hospital Nossa Senhora da Conceicao CRS (12201)
    • Contact: Rita de Cassia Alves Lira; Phone Number: +55 51-33572603; Email: lrita@ghc.com.br
• Mexico
  • Tlalpan
    • Mexico City, Tlalpan, Mexico, 14080
      • Not yet recruiting
      • Nutrición-Mexico CRS (32078)
      • Contact: Brenda Eloisa Crabtree-Ramirez; Phone Number: 52-5555130010; Email: brenda.crabtree@infecto.mx
• Peru
  • Lima, Peru, 4
    • Not yet recruiting
    • Barranco CRS (11301)
    • Contact: María del Pilar Estrella Caballero; Phone Number: +51 206-7800; Email: mestrella@impactaperu.org
• Philippines
  • Cavite, Philippines, 4114
    • Not yet recruiting
    • De La Salle Health Science Institute Angelo King Medical Research Center (DLSHSI-AKMRC) (31981)
    • Contact: Maria Tarcela Gler; Phone Number: +63 917-823-0431; Email: msgler@my.dlshsi.edu.ph
• South Africa
  • Johannesburg, South Africa, 1864
    • Not yet recruiting
    • Soweto ACTG CRS (12301)
    • Contact: Suri Moonsamy; Phone Number: +27-11-989-9905; Email: moonsamys@phru.co.za
• Thailand
  • Chiang Mai, Thailand, 50200
    • Not yet recruiting
    • Chiang Mai University HIV Treatment (CMU HIV Treatment) CRS (31784)
    • Contact: Daralak Tavornprasit; Phone Number: 176 66 5393 6148; Email: daralak.t@cmu.ac.th
  • Patumwan
    • Bangkok, Patumwan, Thailand, 10330
      • Not yet recruiting
      • Thai Red Cross AIDS Research Centre (TRC-ARC) CRS (31802)
      • Contact: Parawee Thongpaeng; Phone Number: 106 66-2-6523040; Email: parawee.t@hivnat.org
• United States
  • California
    • San Diego, California, United States, 92103
      • Not yet recruiting
      • UCSD Antiviral Research Center CRS (701)
      • Contact: Steven Hendrickx; Phone Number: 619-543-6968; Email: smhendrickx@health.ucsd.edu
    • San Francisco, California, United States, 94110
      • Recruiting
      • University of California, San Francisco HIV/AIDS CRS (801)
      • Contact: Elvira Gomez; Phone Number: 415-476-4082; Email: elvira.gomez@ucsf.edu
  • Colorado
    • Aurora, Colorado, United States, 80045
      • Not yet recruiting
      • University of Colorado Hospital CRS (6101)
      • Contact: Nicola Haakonsen; Phone Number: 303-724-5931; Email: nicola.haakonsen@cuanschutz.edu
  • District of Columbia
    • Washington, District of Columbia, United States, 20005
      • Not yet recruiting
      • Whitman-Walker Institute, Inc. CRS (31791)
      • Contact: Avery Wimpelberg; Phone Number: 202-797-3589; Email: awimpelberg@whitman-walker.org
  • Georgia
    • Atlanta, Georgia, United States, 30308
      • Recruiting
      • The Ponce de Leon Center CRS (5802)
      • Contact: Ericka Patrick, M.S.N.; Phone Number: 404-616-6313; Email: erpatri@emory.edu
  • Maryland
    • Baltimore, Maryland, United States, 21205
      • Not yet recruiting
      • Johns Hopkins University CRS (201)
      • Contact: Rebecca L. Becker; Phone Number: 410-614-4036; Email: rbecke22@jhmi.edu
  • Massachusetts
    • Boston, Massachusetts, United States, 02114
      • Not yet recruiting
      • Massachusetts General Hospital CRS (MGH CRS) (101)
      • Contact: Amy Sbrolla; Phone Number: 617-726-5598; Email: asbrolla@mgh.harvard.edu
  • Missouri
    • Saint Louis, Missouri, United States, 63110-1010
      • Recruiting
      • Washington University Therapeutics (WT) CRS (2101)
      • Contact: Michael Klebert; Phone Number: 314-454-0058; Email: mklebert@wustl.edu
  • New Jersey
    • Newark, New Jersey, United States, 07103
      • Not yet recruiting
      • New Jersey Medical School Clinical Research Center CRS (31786)
      • Contact: Rondalya DeShields; Phone Number: 973-972-3729; Email: deshierd@njms.rutgers.edu
  • New York
    • New York, New York, United States, 10010
      • Not yet recruiting
      • Weill Cornell Chelsea CRS (7804)
      • Contact: Rebecca Fry; Phone Number: 212-746-7204; Email: ref2007@med.cornell.edu
    • New York, New York, United States, 10032-3732
      • Not yet recruiting
      • Columbia Physicians & Surgeons (P&S) CRS (30329)
      • Contact: Mascha Elskamp; Phone Number: 212-305-2201; Email: me2500@cumc.columbia.edu
    • New York, New York, United States, 10065
      • Recruiting
      • Weill Cornell Uptown CRS (site 7803)
      • Contact: Jonathan Berardi; Phone Number: 212-746-7864; Email: jlb4002@med.cornell.edu
  • North Carolina
    • Chapel Hill, North Carolina, United States, 27599-7215
      • Not yet recruiting
      • Chapel Hill CRS (3201)
      • Contact: Susan Pedersen; Phone Number: 919-966-6713; Email: spederse@med.unc.edu
    • Greensboro, North Carolina, United States, 27401
      • Recruiting
      • Greensboro CRS (3203)
      • Contact: Kim Epperson, RN, BSN, CRC; Phone Number: 336-832-3262; Email: kim.epperson@conehealth.com
  • Ohio
    • Cleveland, Ohio, United States, 44106
      • Not yet recruiting
      • Case CRS (2501)
      • Contact: Julie Pasternak; Phone Number: 216-844-2738; Email: pasternak.julie@clevelandactu.org
    • Columbus, Ohio, United States, 43210-1282
      • Not yet recruiting
      • Ohio State University CRS (2301)
      • Contact: Lindsay Summers; Phone Number: 614-293-8529; Email: lindsay.summers@osumc.edu
  • Tennessee
    • Nashville, Tennessee, United States, 37204
      • Recruiting
      • Vanderbilt Therapeutics CRS
      • Contact: Beverly Woodward; Phone Number: 615-936-8516; Email: beverly.o.woodward@vumc.org
  • Texas
    • Houston, Texas, United States, 77030
      • Recruiting
      • Houston AIDS Research Team CRS (31473)
      • Contact: Maria Laura Martinez; Phone Number: 713-500-6718; Email: Maria.L.Martinez@uth.tmc.edu
  • Washington
    • Seattle, Washington, United States, 98104
      • Not yet recruiting
      • University of Washington Positive Research CRS (1401)
      • Contact: Christine Jonsson; Phone Number: 206-744-8886; Email: cjonsson@uw.edu
• Vietnam
  • Hanoi, Vietnam
    • Not yet recruiting
    • Hanoi Medical University (HMU) (32482)
    • Contact: Ha Viet Tran; Phone Number: 84-24-3211-5839; Email: vietha@live.unc.edu

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. Age greater than or equal to 18 years.
2. Documentation of HIV-1 status.
3. Assigned male sex at birth and identifies as a TW, female or transfeminine person.
4. On ART for at least 24 weeks prior to study entry. Regimen changes within the 24 weeks prior to study entry are acceptable, but candidates must have been on a stable regimen for at least 28 days prior to study entry.
5. On BIC/FTC/TAF, DTG/TDF/FTC or 3TC, or DRV/c-containing ART for at least 28 days prior to study entry (single tablet regimen not required), and with no plans to change ART regimen over the study duration of 48 weeks.
6. Desire to initiate or restart FHT, regardless of orchiectomy status.
7. HIV-1 RNA <200 copies/mL at screening.
8. HIV-1 RNA <400 copies/mL available through routine clinical care between 24 and 96 weeks prior to study entry and while on ART. The HIV-1 RNA must be the most recent value obtained between 24 and 96 weeks prior to study entry.

9. The following laboratory values obtained within 60 days prior to study entry

   • Hemoglobin ≥9.0 g/dL
   • Platelet count ≥75,000/mm3
   • Estimated Glomerular Filtration Rate (eGFR) ≥30 mL/min/1.73m2 if on or switching to TAF, ≥50 mL/min/1.73m2 if on or switching to TDF without cobicistat, or ≥70 mL/min/1.73m2 if on or switching to TDF in combination with cobicistat, calculated using the CKD-Epi equation
   • Aspartate aminotransferase (AST) (SGOT), alanine aminotransferase (ALT) (SGPT), and alkaline phosphatase are within normal range per local laboratory range
   • Prolactin <25 ng/dL
10. Serum estradiol level <75 pg/mL within 60 days prior to study entry.
11. Willingness to avoid the use of prescribed, non-study provided FHT and non-prescribed FHT during the study period, and no planned use of prescribed or non-prescribed anti-androgens for the first 24 weeks of the study.
12. Ability and willingness of participant to provide informed consent and ability and willingness of participant to undergo study procedures.

Exclusion Criteria:

1. Known clotting disorders, active deep vein thrombosis (DVT), pulmonary embolism (PE), or history of these conditions, active arterial thromboembolic disease (e.g., stroke, myocardial infarction), or history of these conditions.
2. Known liver impairment or disease.
3. History of chronic hepatitis B virus (HBV) infection or active HBV infection.
4. History of current active hepatitis C virus (HCV) infection.
5. Prohibited medication use (including drugs with known or expected DDIs with FHT or ART) at time of study entry.
6. Receipt of any estrogen therapy within 14 days prior to study entry for persons on oral FHT, or within 30 days prior to entry for persons on injectable FHT.
7. Known HIV-1 resistance mutations that would preclude remaining on current ART or a switch to a study regimen, in the opinion of the site investigator.
8. Personal history of breast cancer. or known personal history of breast cancer (BRCA) gene.
9. Known or a history of testicular cancer.
10. Known or a history of gall bladder disease.
11. Known or suspected pituitary adenoma.
12. Known allergy/sensitivity or any hypersensitivity to components of study drugs or their formulation.
13. Known allergy/sensitivity or any hypersensitivity to components of study drugs or their formulation.
14. Suicidal ideation in the past 30 days or suicide attempt in the past 90 days, as reported on the Columbia-Suicide Severity Rating Scale (C-SSRS).
15. Serious illness requiring systemic treatment and/or hospitalization within 30 days prior to entry. Stable (in the opinion of the site investigator) treatments for chronic comorbidities are allowed.
16. Presence of any other medical condition that would preclude FHT administration for safety reasons, in the opinion of the site investigator.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Group 1: BIC-treated; Participants taking bictegravir (BIC) + tenofovir alafenamide (TAF) + emtricitabine (FTC)	Drug: Estradiol; Oral 17-β estradiol 2 mg once daily will be initiated at study entry. At weeks 4, 12, 24, and 36, study clinicians may titrate 17-β estradiol in 2 mg increments to achieve the desired participant goals and target hormone concentrations, as measured locally at each visit.
Experimental: Group 2: DTG-treated; Participants taking dolutegravir (DTG) once daily + tenofovir disoproxil fumarate (TDF) + (FTC or lamivudine [3TC])	Drug: Estradiol; Oral 17-β estradiol 2 mg once daily will be initiated at study entry. At weeks 4, 12, 24, and 36, study clinicians may titrate 17-β estradiol in 2 mg increments to achieve the desired participant goals and target hormone concentrations, as measured locally at each visit.
Experimental: Group 3: Boosted DRV-treated; Participants taking any regimen containing darunavir plus cobicistat (DRV/c)	Drug: Estradiol; Oral 17-β estradiol 2 mg once daily will be initiated at study entry. At weeks 4, 12, 24, and 36, study clinicians may titrate 17-β estradiol in 2 mg increments to achieve the desired participant goals and target hormone concentrations, as measured locally at each visit.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Geometric Mean Ratio of ART Analytes BIC, DTG, and DRV trough concentrations (Ctrough) in plasma at each received dose of oral 17-β estradiol	Log-transformed trough concentrations (Ctrough) in ng/mL of the analytes BIC, DTG, and DRV from plasma samples collected 22-26 hours post ART dose, measured over 48 weeks.	Study Entry and Weeks 4, 12, 24, 36, and 48
Percentage of Participants with ART Analyte trough concentration (Ctrough) above drug-specific threshold	Trough concentration of the analytes BIC, DTG, and DRV in plasma at each received dose of 17-β estradiol summarized at the participant level as indicator of concentration being above drug-specific threshold.	Study Entry and Weeks 4, 12, 24, 36, and 48
Trough serum total estradiol assessed at each received dose of oral 17-β estradiol as quantified via batch testing at central lab.	Trough concentrations of Total 17-β estradiol in ng/mL from serum samples collected 22-26 hours post 17-β estradiol dose. Results < Lower Limit of Quantification (LLoQ) at entry will be imputed as 0 ng/mL at one-half the LLoQ value at visits post-entry.	Study Entry and Weeks 4, 12, 24, 36, and 48

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Trough concentrations of TFV-DP, FTC-TP, and 3TC-TP in non-viable PBMCs at each received dose of oral 17-β estradiol	Intra-person geometric ratios of trough ART concentration at each received estradiol dose relative to pre-FHT (i.e., baseline).	Study Entry and Weeks 4, 12, 24, 36 and 48
Percentage of Participants with TFV-DP, FTC-TP, and 3TC-TP trough concentration above drug-specific threshold	Trough concentration of the analytes TFV-DP, FTC-TP, and 3TC-TP in non-viable PBMCs at each received dose of 17-β estradiol summarized at the participant level as indicator of concentration being above drug-specific externally defined threshold.	Study Entry and Weeks 4, 12, 24, 36 and 48
Percentage of participants with an occurrence of any reportable adverse event related to 17-β estradiol	The Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events (DAIDS AE Grading Table), corrected Version 2.1, July 2017, and the DAIDS EAE Manual Version 2.0 will be used.	Study entry to Week 48
Percentage of participants with an occurrence of SAEs as defined by International Conference on Harmonization (ICH) and new events of CAD/CVD, cancer, DM/pre-DM, and vascular event	Post-entry and while on study treatment, all signs (including an abnormal laboratory finding), symptoms, or diagnoses new in onset or aggravated in severity or frequency from the baseline condition, indicated as related to 17-β estradiol by the site (or the CMC if adjudication differs from that of the site investigator).	Study entry to Week 48
Percentage of participants with serum total testosterone < 50 ng/dL at each received dose of oral 17-β estradiol	Results < LLoQ will be considered to be <50 ng/dL. If multiple observations are available at the same estradiol dose, the last testosterone concentration (based on calendar time) taken will be used.	Study entry and Weeks 4, 12, 24, 36, 48
Percentage of participants with virologic suppression of HIV	Virologic suppression of HIV is defined as plasma HIV-1 viral load <50 copies/mL	Study entry and weeks 12, 24, 36, and 48
Absolute changes in overall transgender congruence score	The overall transgender congruence score is calculated from participant response to the 12-question Transgender Congruence Scale (TCS). Participants rate each item on a 5-point Likert-type scale (i.e., 1 = strongly disagree, 2 = somewhat disagree, 3 = neither agree nor disagree, 4 = somewhat agree, 5 = strongly agree). Questions 'The way my body currently looks does not represent my gender identity.', 'I do not feel that my appearance reflects my gender identity.', and 'I am not proud of my gender identity.' are reversed scored. The overall score is the average of the response to the 12 questions, with higher scores indicating a higher level of congruence. Positive changes from baseline indicate improvement in transgender congruence.	Study entry and weeks 24, and 48
Area under the curve over 8 hours (AUC 0-8h) of 17-β estradiol	From pre-dose, 1, 2, 3, 4, 6, and 8 hours post dosing at entry and weeks 24 and 48. The AUC will use the linear up/log down version of the trapezoidal rule in non-compartmental analysis using Phoenix WinNonLin (Certara®). This version of the trapezoidal rule uses linear interpolation between untransformed data up to Cmax, and between log-transformed data from Cmax through Clast.	Study entry and Weeks 24, and 48
Percent change in weight	Calculated by dividing weight at later time point minus weight at study entry by weight at study entry.	Study entry and weeks 12, 24, 36, and 48
Percent change in BMI	Calculated by dividing BMI at later time point minus BMI at study entry by BMI at study entry.	Study entry and weeks 12, 24, 36, and 48
Absolute change in minimum waist circumference	Calculated as waist circumference at later time point minus waist circumference at study entry.	Study entry and weeks 12, 24, 36, and 48
Absolute change in maximum hip circumference	Calculated as maximum hip circumference at later time point minus maximum hip circumference at study entry.	Study entry and weeks 12, 24, 36, and 48
Absolute change in waist-hip ratio measured	Calculated as waist-hip ratio at later time point minus waist-hip ratio at study entry.	Study entry and weeks 12, 24, 36, and 48
Absolute changes in fasting lipids	Calculated as fasting lipids at later time point minus fasting lipids at study entry.	Study entry and weeks 12, 24, and 48
Absolute changes in glucose sensitivity	Calculated as glucose sensitivity at later time point minus glucose sensitivity at study entry.	Study entry and weeks 12, 24, 36, and 48
Absolute changes in insulin sensitivity	Calculated as insulin sensitivity at later time point minus insulin sensitivity at study entry. Insulin will be measured from stored samples. Insulin sensitivity will be calculated as: HOMA-IR = (fasting glucose in mmol/L * fasting insulin in µU/L) /22.5.	Study entry and weeks 12, 24, 36, and 48

Collaborators and Investigators

• Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)
• Investigators: Study Chair: Jordan E. Lake, MD, MSc, Houston AIDS Research Team CRS; Study Chair: Kimberly K. Scarsi, PharmD, MS, FCCP, University of Nebraska; Study Chair: Jorge A. Gallardo-Cartagena, MD, Barranco CRS

Study record dates

Study Major Dates

• Study Start (Actual): January 4, 2024
• Primary Completion (Estimated): May 8, 2027
• Study Completion (Estimated): May 8, 2027

Study Registration Dates

• First Submitted: August 15, 2023
• First Submitted That Met QC Criteria: August 15, 2023
• First Posted (Actual): August 22, 2023

Study Record Updates

• Last Update Posted (Estimated): April 15, 2024
• Last Update Submitted That Met QC Criteria: April 12, 2024
• Last Verified: April 1, 2024

More Information

Terms related to this study

• Keywords: HIV; Transgender women; Estradiol; Drug interactions; ART
• Additional Relevant MeSH Terms: Physiological Effects of Drugs; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Estrogens; Estradiol
• Other Study ID Numbers: A5403; 38806 (Other Identifier: DAIDS-ES ID)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Individual participant data that underlie results in the publication, after deidentification.
• IPD Sharing Time Frame: Beginning 3 months following publication and available throughout period of funding of the AIDS Clinical Trials Group by NIH.
• IPD Sharing Access Criteria: With whom? Researchers who provide a methodologically sound proposal for use of the data that is approved by the AIDS Clinical Trials Group.; For what types of analyses? To achieve aims in the proposal approved by the AIDS Clinical Trials Group.; By what mechanism will data be made available? Researchers may submit a request for access to data using the AIDS Clinical Trials Group "Data Request" form at: https://actgnetwork.org/submit-a-proposal/. Researchers of approved proposals will need to sign an AIDS Clinical Trials Group Data Use Agreement before receiving the data.
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL; SAP

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No