Co-benefits of Co-delivery of Long-acting Antiretrovirals and Contraceptives
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 700
- 试验地点
- 1
- 主要终点
- Hormone concentrations with cabotegravir/rilpivirine use (Aim 1a)
研究概览
简要总结
The study investigators are conducting foundational pharmacokinetic (PK) and qualitative studies, among 15-24 years old (inclusive) adolescent girls and young women living with HIV (AGYWLHIV) already on oral antiretroviral therapy (ART) and virally suppressed, leading up to a hybrid type I effectiveness-implementation trial randomizing individual AGYWLHIV to receive long-acting (LA) injectable cabotegravir/rilpivirine vs. standard of care within one of Kenya's largest HIV treatment programs. The PK and qualitative studies will investigate potential issues arising from co-delivery and guide delivery of the effectiveness-implementation trial. The PK and qualitative studies will largely be conducted with a sentinel cohort of AGYWLHIV. Learning from this early LA ART use, the investigators will refine the procedures in the LA ART hybrid trial.
详细描述
Long-acting (LA) antiretroviral therapy (ART), such as injectable cabotegravir and rilpivirine, has been receiving global clinical approvals and has the potential to address barriers to ART and improve patient adherence and persistence to treatment. LA ART regimens can potentially also increase options for patients and providers to individualize treatment plans, provide a powerful treatment option for those experiencing adherence issues related oral treatment options, and may ease the burden of health systems in RLS. Another major threat to AGYW's health is unintended pregnancies and AGYWLHIV also face unique challenges in uptake and continuation of LA contraceptives. Use of LA ART may foster synergy in usage of LA contraceptives among AGYWLHIV.
This proposed research study has three main components: 1) a prospective, non-randomized, parallel-group pharmacokinetic (PK) study among a sentinel cohort of five distinct groups of AGYW, and will leverage existing control groups (Aim 1a); 2) a qualitative study that will conduct individual interviews with four different subgroups of AGYWLHIV from the sentinel cohort from the PK study, as well as focus group discussions with providers, policy makers, and other stakeholders for health systems readiness for wider scale-up (Aim 1b); and 3) an open-label, mixed methods, 48-week type I hybrid trial randomizing AGYW with viral suppression on their current ART regimen to switch to 1:1 cabotegravir/ rilpivirine (intervention arm) vs. continue their oral ART regimen (Aim 2a), with a component also evaluating implementation outcomes of acceptability, feasibility, and fidelity (Aim 2b). The proposed study will be conducted in HIV treatment facilities in western Kenya within the regional Moi Teaching and Referral Hospital (MTRH).
This study will provide foundational data for future studies and implementation plans related to addressing barriers and will critically inform follow-up studies of LA ART in other priority subpopulations. Providing an array of method options for both HIV treatment and pregnancy prevention has the potential to revolutionize personal decision-making and improve long-term outcomes for AGYWLHIV. Our real-world experiences of co-delivery will also inform future considerations for co-formulations of antiretrovirals and contraceptives for both HIV treatment and prevention.
Our central hypothesis is the following: 1) at the client level, the use of LA ART or contraceptives will foster long-term thinking for health, forging a convergence of the use of the two when applicable; and 2) at the program/provider level, leveraging existing LA contraceptive delivery platform will make LA ART highly acceptable, feasible, and deliverable with high fidelity.
Our overall objective in this study is to conduct the foundational PK and qualitative studies first as a lead in to the hybrid trial. Guided by Proctor et al.'s implementation outcomes framework, the hybrid trial will also focus on acceptability, feasibility, and fidelity. These implementation outcomes are proximal indicators of implementation processes and intermediate outcomes, which ultimately predict implementation success. Demonstrating successful implementation outcomes will then inform wider-scale implementation of LA ART, when service and client outcomes can be fully realized.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Investigator, Outcomes Assessor)
盲法说明
Participants and care providers will not be masked (open label), but the principle and site-principal investigators and study statistician will be blinded to arm allocation.
入排标准
- 年龄范围
- 15 Years 至 24 Years(Child, Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •(PK study):
- •Female sex,
- •HIV-positive (for PK groups #1-4) or HIV-uninfected (for PK group #5 only),
- •Age 15-24 years at the time of enrollment,
- •Documented or confirmed viral suppression for HIV (defined as <40 copies/mL) within 6 months prior to study enrollment,
- •Have been on the study oral drug for at least 4 weeks for the PK groups #1-4,
- •Have initiated and intends to use DMPA or implant for at least another three or 6 months, respectively,
- •Willing to undergo phlebotomy every 4-12 weeks for the duration of the study period
- •Able to consent or assent (with parental consent) for study participation in English or Kiswahili
排除标准
- •(PK study):
- •Already be on ART that concurrently contains combinations of non-nucleoside reverse transcriptase inhibitors (NNRTIs), such as efavirenz, and protease-inhibitors (PIs), such as atazanavir/ritonavir or lopinavir/ritonavir, or integrase inhibitors (INSTIs), such as raltegravir or dolutegravir
- •Currently pregnant or intends to become pregnant or breastfeeding within the next 12 or 24 weeks for DMPA or implant groups, respectively,
- •Have had unprotected sex in the last two weeks or be currently pregnant via urine pregnancy testing,
- •Use or anticipated use of drugs for the duration of the study period known to interact with hormonal implants or the study ART regimen,
- •Current or planned concomitant use of other hormonal contraceptives,
- •Be obese (BMI≥30),
- •Evidence of Hepatitis B virus (HBV) infection based on the results of testing for Hepatitis B surface antigen (HBsAg), Hepatitis B core antibody (anti-HBc), Hepatitis B surface antibody (anti-HBs) and HBV Deoxyribonucleic acid (DNA) as follows: positive for HBsAg being excluded or negative for anti-HBs but positive for anti-HBc (negative HBsAg status) and positive for HBV DNA are excluded (of note, participants positive for anti-HBc (negative HBsAg status) and positive for anti-HBs (past and/or current evidence) are immune to HBV and are not excluded).
- •Serum ALT>5x ULN at the time of screening,
- •Serum creatinine >2.5x ULN at the time of screening.
- •Inclusion Criteria Aim 1b (qualitative PK study):
- •Participating in PK study for study participants,
- •Self-identifying as provider, program person, policy-maker, or stakeholder relevant to the study topics, and age 18 years of age or older,
- •Able to consent for study participation in English or Kiswahili
- •Inclusion Criteria (Hybrid trial):
- •Female sex,
- •HIV-positive,
- •Age 15-24 years at the time of enrollment,
- •Documented or confirmed viral suppression for HIV (defined as <40 copies/mL) within 6 months prior to study enrollment,
- •Willing to undergo phlebotomy every 4-12 weeks for the duration of the study period,
- •Able to consent or assent (with parental consent) for study participation in English or Kiswahili
- •Exclusion Criteria (Hybrid trial):
- •Already be on ART that concurrently contains combinations of non-nucleoside reverse transcriptase inhibitors (NNRTIs), such as efavirenz, and protease-inhibitors (PIs), such as atazanavir/ritonavir or lopinavir/ritonavir, or integrase inhibitors (INSTIs), such as raltegravir or dolutegravir
- •Currently pregnant or intends to become pregnant or breastfeeding within the next one year,
- •Have had unprotected sex in the last two weeks or be currently pregnant via urine pregnancy testing,
- •Use or anticipated use of drugs for the duration of the study period known to interact with the study ART regimen,
- •Evidence of Hepatitis B virus (HBV) infection based on the results of testing for Hepatitis B surface antigen (HBsAg), Hepatitis B core antibody (anti-HBc), Hepatitis B surface antibody (anti-HBs) and HBV Deoxyribonucleic acid (DNA) as follows: positive for HBsAg being excluded or negative for anti-HBs but positive for anti-HBc (negative HBsAg status) and positive for HBV DNA are excluded (of note, participants positive for anti-HBc (negative HBsAg status) and positive for anti-HBs (past and/or current evidence) are immune to HBV and are not excluded).
- •Serum ALT>5x ULN at the time of screening,
- •Serum creatinine >2.5x ULN at the time of screening.
- •Inclusion Criteria Aim 2b (qualitative study):
- •Participating in hybrid trial study for study participants,
- •Self-identifying as provider, program person, policy-maker, or stakeholder relevant to the study topics, and age 18 years of age or older,
- •Able to consent for study participation in English or Kiswahili
研究组 & 干预措施
Aim 1a (PK study group 2)
Initiating injectable cabotegravir/rilpivirine (LA ART) and and etonogestrel implant
干预措施: Etonogestrel (ETG) implant (Drug)
Aim 1a (PK study group 3)
Initiating injectable cabotegravir/rilpivirine (LA ART) and levonorgestrel implant.
干预措施: Levonorgestrel (Drug)
Aim 1a (PK study group 5)
AGYW without HIV and not exposed to antiretrovirals (e.g., for PrEP) initiating DMPA
干预措施: Intramuscular depo-medroxyprogesterone acetate (IM DMPA) (Drug)
Aim 1a (PK study group 1)
Initiating injectable cabotegravir/rilpivirine (LA ART) and DMPA
干预措施: Intramuscular depo-medroxyprogesterone acetate (IM DMPA) (Drug)
Aim 2a (Hybrid trial comparator group)
AGYW with viral suppression to continue their oral ART regimen.
干预措施: NNRTI, PI, or INSTI-containing 1st or 2nd line ART regimens (Drug)
Aim 2a (Hybrid trial intervention group)
AGYW with viral suppression on their current ART regimen to switch to cabotegravir/ rilpivirine.
干预措施: Cabotegravir/ Rilpivirine (Drug)
Aim 1a (PK study group 2)
Initiating injectable cabotegravir/rilpivirine (LA ART) and and etonogestrel implant
干预措施: Cabotegravir/ Rilpivirine (Drug)
Aim 1a (PK study group 1)
Initiating injectable cabotegravir/rilpivirine (LA ART) and DMPA
干预措施: Cabotegravir/ Rilpivirine (Drug)
Aim 1a (PK study group 4)
Receiving injectable cabotegravir/ rilpivirine (LA ART) and not using any hormonal contraceptive method (e.g. copper IUD)
干预措施: Cabotegravir/ Rilpivirine (Drug)
Aim 1a (PK study group 3)
Initiating injectable cabotegravir/rilpivirine (LA ART) and levonorgestrel implant.
干预措施: Cabotegravir/ Rilpivirine (Drug)
结局指标
主要结局
Hormone concentrations with cabotegravir/rilpivirine use (Aim 1a)
时间窗: 12 or 24 weeks after DMPA or implant initiation, respectively
To assess differences in hormone concentrations with cabotegravir/rilpivirine use, the investigators will first calculate the progestin geometric mean concentrations at 12 or 24 weeks after DMPA or implant initiation, respectively, for each group. These geometric means will be compared to HIV-negative groups recruited in this study (for the DMPA comparator) or from the PARVI study (for the implants comparator), using geometric mean ratios with 90% confidence intervals (a FDA standard) and the Wilcoxon rank sum test.
Number of participants with HIV viral suppression (Aim 2a)
时间窗: 48 weeks after study enrollment
Our primary analysis will compare the proportion of participants with viral suppression (via HIV viral load \<40 copies/mL) 48 weeks after study enrollment (primary outcome) in the intervention vs. control arms (primary exposure) using logistic regression, adjusting for age group strata.
次要结局
- Adherence to ART (Aim 2a)(3, 6, and 12 months after method initiation)
- Persistence to ART (Aim 2a)(3, 6, and 12 months after method initiation)
- Contraceptive outcome (Aim 2a)(3, 6, and 12 months after method initiation)
研究者
Rena Patel
Principal Investigator
University of Alabama at Birmingham
