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Cabotegravir-Hormone PK/PD Interactions for HIV Prevention (CHIPP-PrEP)

10 juli 2026 uppdaterad av: Johns Hopkins University

CHIPP-PrEP: Cabotegravir-Hormone Interrogation of Pharmacokinetics/Pharmacodynamics (PK/PD) for HIV Prevention

This is a research study to better understand how long-acting cabotegravir (CAB-LA) works to prevent HIV in people. This study will also evaluate the impact of endogenous and therapeutic hormones on CAB-LA pharmacology. The investigators will also evaluate if participants experience any medical problems when taking CAB-LA.

Studieöversikt

Status

Rekrytering

Betingelser

Detaljerad beskrivning

The CHIPP-PrEP protocol is a phase 1, open label study to compare the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of long-acting cabotegravir injectable (CAB-LA) administration in adults aged 19 years or older. Long-acting cabotegravir (Apretude™) is an FDA-approved injectable antiretroviral medication administered every two months for HIV pre-exposure prophylaxis (PrEP). While clinical efficacy trials have demonstrated CAB-LA's effectiveness in preventing HIV infection, knowledge gaps remain regarding drug penetration into mucosal tissues where HIV transmission primarily occurs and potential drug-drug interactions with therapeutic hormone therapies. Current PK data derives predominantly from plasma measurements, which may not accurately reflect drug concentrations at actual sites of HIV exposure in rectal and genital mucosa. This study addresses these critical gaps by directly measuring CAB-LA concentrations in blood, mucosal tissues, and genital secretions across three distinct population cohorts: males not using exogenous hormones, males using therapeutic hormone therapy, and females using non-hormonal contraception. This design enables isolation of hormone effects on CAB-LA pharmacokinetics while controlling for biological sex differences.

Following successful screening, eligible participants will return for a Baseline Visit (Day 0) to complete pre-treatment evaluations. At baseline, participants will undergo laboratory assessment of circulating hormone concentrations (estradiol and testosterone), HIV antibody/antigen and RNA testing to confirm HIV-negative status, and collection of rectal biopsies (all participants) and cervical biopsies (females only) for baseline HIV explant challenge pharmacodynamic assessment. These baseline tissue samples undergo ex vivo HIV-1 challenge experiments to establish pre-treatment viral susceptibility prior to CAB-LA exposure. One week following baseline biopsy collection (Visit 1, Day 7), participants will be administered a single 3 mL intramuscular injection of 600 mg cabotegravir long-acting injectable suspension (Apretude™, ViiV Healthcare; 200 mg/mL formulation) using the recommended ventrogluteal approach by licensed clinical staff.

Biopsy Collection Visits will occur at study visits 2,4, 6, 7, and 8 (Days 7, 14, 35, 63, and 91). At these intensive study visits, blood will be collected for hormone testing (estradiol and testosterone), plasma CAB-LA concentration determination, and eGFR monitoring. Rectal fluid and cervicovaginal fluid will be collected using specialized swabs to measure mucosal drug concentrations. Rectal biopsies (all participants) and cervical biopsies (females only) will be collected using flexible sigmoidoscopy and standard gynecological techniques, respectively, for both tissue drug concentration measurement and pharmacodynamic HIV explant challenge experiments.

Interim Pharmacokinetic Visits (Visits 3 and 5 at Days 10 and 21): Blood will be collected for plasma CAB-LA concentration determination, eGFR assessment, and hormone measurements. A final safety visit (Visit 9 at Day 98) will be performed. Select concomitant medications, with particular emphasis on exogenous hormones and medications that may affect cabotegravir or hormone metabolism, will be collected on daily concomitant medication logs maintained by participants throughout the study.

Safety assessments, including history/physical, chemistry/hematology labs at screening and interim history will be performed at study visits

Studietyp

Interventionell

Inskrivning (Beräknad)

32

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

  • Namn: Jennifer Hoffmann
  • Telefonnummer: 4109551318

Studieorter

    • Maryland
      • Baltimore, Maryland, Förenta staterna, 212187
        • Rekrytering
        • Johns Hopkins School of Medicine, Drug Development Unit
        • Kontakt:
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  • 19 years of age or older
  • For persons using exogenous hormones, must be on a stable regimen for ≥6 months and remain on that regimen throughout study conduct, and exogenous hormone regimens must be prescribed and managed under the care of a healthcare professional
  • For females, must be on a non-hormonal contraceptive agent, and must persist in contraceptive use for the duration of the study
  • Body weight greater than 35 kg (77.2 lbs)
  • HIV-1 uninfected at screening and enrollment as documented by an instrumented Ag/Ab assay and HIV-1 RNA testing
  • Understand and agree to local STI reporting requirements
  • Willing to abstain from additional antiretroviral agents (including PrEP agents, F/TAF and F/TDF) during the duration of the study
  • Willing to abstain from insertion of anything (drug, enema, penis, or sex toy) in the rectum or vagina for 72 hours before and 72 hours after each flexible sigmoidoscopy
  • Willing to refrain from aspirin and NSAID use for one week before and after each study biopsy visit
  • Willing and able to use condoms for all receptive anal intercourse and receptive vaginal intercourse for the duration of study participation
  • Able and willing to communicate in English
  • Able and willing to provide written informed consent to take part in the study
  • Able and willing to provide adequate information for locator purposes
  • Availability to return for all study visits, barring unforeseen circumstances
  • Agree not to participate in other research studies involving drugs and/or medical devices for the duration of the study

Exclusion Criteria:

  • History of previous long-acting antiretroviral use, including CAB-LA and long-acting lenacapavir
  • History of oral PrEP (F/TDF, F/TAF) use within the prior eight weeks
  • For females, if a participant is pregnant or plans to become pregnant during study duration
  • For females, if the participant is actively breastfeeding
  • For females, if the participant is post-menopausal or accessing exogenous hormone replacement therapy
  • For females, has irregular menstrual cycles
  • Has a tattoo or other dermatological condition which may interfere with product administration or interpretation of injection site reactions
  • Surgically-placed or injected buttock implants or filler, per self-report
  • One or more reactive or positive HIV test results at screening or enrollment, even if HIV infection is not confirmed
  • Current known HIV-infected partner(s)
  • Symptoms suggestive of acute HIV seroconversion at screening and enrollment
  • Known or suspected allergy to CAB-LA
  • Any ≥ Grade 2 laboratory abnormality at baseline as defined by Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1 - July 2017, and Addendum 3 (Rectal Grading Tables for Use in Microbicide Studies)
  • Significant rectal symptom(s) as determined by medical history or by participant self-report (including but not limited to presence of any unresolved injury, infectious or inflammatory condition of the local mucosa, history of inflammatory bowel disease, presence of symptomatic hemorrhoids, and presence of any painful anorectal conditions that would be tender to manipulation)
  • At screening or within the past 2 months: participant-reported symptoms and/or clinical or laboratory diagnosis of active rectal or genital infection requiring treatment per current CDC guidelines or symptomatic urinary tract infection (UTI). Infections requiring treatment include chlamydia (CT), gonorrhea (GC), syphilis, active HSV lesions, chancroid, genital sores or ulcers, and, if clinically indicated, genital warts. HSV seropositivity with no active genital lesions is not an exclusion criterion. (Note: if an STI apart from HIV is detected, the participant will be referred for treatment and can be retested in 30 days and re-screened once.)
  • History of significant gastrointestinal bleeding
  • Clinically significant cardiovascular disease, as defined by history of symptomatic arrhythmia, ischemia, or other significant cardiac disease
  • Current use of warfarin or heparin or other anticoagulant medications associated with increased risk for bleeding following mucosal biopsy (e.g., daily high dose aspirin [>81 mg], NSAIDs, or Pradaxa®)
  • Use of systemic or anorectal immunomodulatory medications within 4 weeks of enrollment or planned use at any time during study participation
  • Per participant report, use of any rectally or vaginally administered products containing N-9 (including condoms) or investigational products within 4 weeks of enrollment, or planned use of either at any time during study participation
  • Any other condition or prior therapy that, in the opinion of the investigator, would preclude informed consent, make study participation unsafe, make the individual unsuitable for the study or unable to comply with the study requirements.
  • Individuals with neocervix will be excluded from giving cervical biopsies, if eligible for study participation.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Single arm for CHIPP-Prep: CAB
A single dose of 600 mg CAB-LA (ApretudeTM; 200 mg/mL) will be prescribed and administered only once during the study. ApretudeTM manufactured by ViiV Healthcare and is a sterile white to slightly pink suspension containing 200 mg/mL of CAB as free acid for administration by intramuscular injection. The product is packaged in a 3 mL USP Type I glass vial with a 13 mm gray stopper and aluminum seal. Each vial is for single use containing a withdrawable fill of 2.0 mL and does not require dilution prior to administration. CAB LA injectable suspension is to be stored at up to 30°C, do not freeze. The dose selected is the FDA-recommended CAB-LA PrEP dose.
Andra namn:
  • Apretud

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Plasma CAB area under the concentration curve
Tidsram: 0-12 weeks, AUC inf
Plasma CAB area under the concentration curve in ng.h/mL from time 0 to week 12 (AUC0-Wk12) and infinity (AUC0-inf), stratified by sex and therapeutic hormone status
0-12 weeks, AUC inf
Plasma CAB concentration
Tidsram: Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Plasma CAB concentration in ng/mL, stratified by sex and therapeutic hormone status
Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Rectal Tissue CAB concentrations
Tidsram: Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Rectal Tissue CAB concentrations in ng/mg, stratified by sex and therapeutic hormone status
Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Rectal Fluid CAB concentrations
Tidsram: Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Rectal Fluid CAB concentrations in ng/mg, stratified by sex and therapeutic hormone status
Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Cervical Tissue CAB concentrations , in females only
Tidsram: Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Cervical Tissue CAB concentrations in ng/mg
Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Cervicovaginal Fluid CAB concentrations, in females only
Tidsram: Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Cervicovaginal Fluid CAB concentrations in ng/mg
Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Serum Estradiol Concentration
Tidsram: Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Estradiol Concentration in pg/mL, stratified by sex and therapeutic hormone status
Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Testosterone Concentration
Tidsram: Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Testosterone (free, total) Concentration in ng/dL, stratified by sex and therapeutic hormone status
Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Luteinizing Hormone Concentration
Tidsram: Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Luteinizing Hormone Concentration in mIU/mL, stratified by sex and therapeutic hormone status
Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Follicle Stimulating Hormone Concentration
Tidsram: Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Serum Follicle Stimulating Hormone Concentration in mIU/mL, stratified by sex and therapeutic hormone status
Baseline (enrollment), and Day 1 (24 hours), Day 3 (72 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Cervical Tissue explant p24 antigen concentrations
Tidsram: Baseline (enrollment), and Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Cervical Tissue explant p24 antigen concentrations in pg/mL, in female participants
Baseline (enrollment), and Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Rectal Tissue explant p24 antigen concentration
Tidsram: Baseline (enrollment), and Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12
Rectal Tissue explant p24 antigen concentration in pg/mL, stratified by sex and therapeutic hormone status
Baseline (enrollment), and Day 1 (24 hours), Week 1, Week 2, Week 4, Week 8, and Week 12

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Mark A Marzinke, Johns Hopkins School of Medicine

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

7 juli 2026

Primärt slutförande (Beräknad)

1 december 2030

Avslutad studie (Beräknad)

1 december 2031

Studieregistreringsdatum

Först inskickad

22 juni 2026

Först inskickad som uppfyllde QC-kriterierna

22 juni 2026

Första postat (Faktisk)

29 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

13 juli 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

10 juli 2026

Senast verifierad

1 juli 2026

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • IRB00494387
  • R01AI186440 (U.S.S. NIH-anslag/kontrakt)

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

produkt tillverkad i och exporterad från U.S.A.

Ja

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