A Novel Regimen to Prevent Malaria and STI in Pregnant Women With HIV

Phase 2

Completed

• Conditions: Sexually Transmitted Infection; HIV; Pregnancy Malaria
• Interventions: Drug: Azithromycin/TMPS; Drug: Placebo/TMPS

• Registration Number: NCT03431168
• Lead Sponsor: University of Alabama at Birmingham

Brief Summary

More than 3 billion people worldwide are at risk of acquiring malaria and pregnant women living with HIV in Africa are at particular risk. An effective prophylaxis regimen capable of preventing malaria and other common perinatal infections would have great potential to improve adverse birth outcomes. The purpose of this randomized controlled trial is to evaluate a new combination prophylaxis regimen in pregnant women with HIV in Cameroon to determine its efficacy and safety.

Detailed Description

The World Health Organization (WHO) recommends malaria prophylaxis for all pregnant women living in endemic areas in order to reduce maternal anemia, low birth weight and perinatal mortality by 25-45%. The most commonly used regimen is intermittently dosed sulfadoxine-pyrimethamine (SP).Unfortunately, SP prophylaxis is contraindicated for HIV-infected pregnant women since co-administration with TMPS (trimethoprim-sulfamethoxazole) causes serious adverse events. TMPS (Bactrim or Cotrimoxazole) is an effective, well-tolerated, low-cost antibiotic that is used as prophylaxis in HIV-patients with low CD4 counts. It has anti-malarial activity with prophylactic efficacy that is comparable to SP (30-90%). Daily TMPS is recommended as malaria prophylaxis in pregnant women with HIV in many African countries (including Cameroon) but malaria infection rates are high even when medication compliance is excellent; thus, new and improved options are urgently needed. Azithromycin (AZ) is a macrolide antibiotic with activity against malaria, a good safety profile in pregnancy and proven utility as a part of combination malaria prevention regimens (such as SP-AZ). It also has activity against sexually transmitted infections (STI) and perinatal pathogens, including chlamydia (CT), gonorrhea (GC), syphilis and GBS (Streptococcus agalactiae or Group B Streptococcus), a potential but understudied contributor to high rates of newborn sepsis and death in Africa. SP-AZ prophylaxis in HIV-uninfected pregnant women has been reported to reduce prevalence of low birth weight (RR 0.74, 95% confidence interval (CI) 0.6-0.9) and preterm delivery (RR 0.66, 95% CI 0.48-0.91) compared to SP alone.

Thus, the central hypothesis is that a TMPS-AZ combination will be more effective than standard TMPS malaria prophylaxis in pregnant women with HIV, and that it will also decrease STI coinfection. Investigators plan a test-of-concept of the central hypothesis by conducting a double blinded, Phase II randomized controlled trial (RCT).

Study Timeline

• Study First Submitted: 2018-01-02
• Study First Submitted QC: 2018-02-06
• Study First Posted: 2018-02-13
• Study Start: 2018-03-07
• Primary Completion: 2021-01-01
• Study Completion: 2022-01-01
• Results First Submitted: 2022-04-06
• Results First Submitted QC: 2022-04-06
• Results First Posted: 2022-05-04
• Status Verified: 2023-11
• Last Update Submitted: 2023-11-24
• Last Update Posted: 2023-11-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 308

Inclusion Criteria

• Confirmed HIV-infection (documented in medical record)
• Age ≥16 years
• Confirmed pregnancy, <28 weeks estimated gestational age (by best obstetric estimate which may include ultrasound or fundal height and LMP)
• Live singleton pregnancy
• Receiving prenatal care at Mboppi Hospital or Mutengene Hospital
• Plan to receive follow up prenatal care and deliver at study facility
• Capable of providing written informed consent
• Able and agree to come to facility for febrile episodes or acute illness during pregnancy (with reimbursement of transportation costs).
• Agree to avoid antimalarial medications outside of study protocol.

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Exclusion Criteria

• Severe anemia (last hemoglobin <6)
• History of severe adverse reaction to co-trimoxazole or azithromycin
• Active medical problem requiring inpatient evaluation at the time of screening
• Intention of moving far away from the facility during pregnancy or not likely to return for follow up care or delivery
• Signs or symptoms of early or active labor
• History of severe cardiac disease (including congestive heart failure, severe valvular disease or arrhythmias).

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Azithromycin/TMPS	Azithromycin/TMPS	Azithromycin 1 gm po daily x 3 days at enrollment and at each 4 week follow up visit. TMPS double strength 1 tablet po daily.
Placebo/TMPS	Placebo/TMPS	Azithromycin placebo 1 gm po daily x 3 days at enrollment and at each 4 week follow up visit. TMPS double strength 1 tablet po daily.

Primary Outcome Measures

Name	Time	Method
Plasmodium Falciparum Peripheral Parasitemia	At end of pregnancy (>35 weeks) or at delivery	P. falciparum detected by microscopy or polymerase chain reaction (PCR)
Proportion With Composite STI Outcome	will be measured in both groups (>35 weeks) or at delivery	Including chlamydia (NAAT (nucleic acid amplification test) positive) , gonorrhea (NAAT positive), syphilis (non-treponemal and treponemal test positive) infections.

Secondary Outcome Measures

Name	Time	Method
Low Birthweight (<2500 Grams)	at birth	Neonatal weight measured with digital scale
Proportion With Adverse Birth Outcomes	Birth outcomes will be measured at birth for all outcomes except early neonatal mortality defined as within 7 days of birth. Early neonatal mortality will be assessed at a six week follow up phone call.	Composite measure: low infant birthweight (\<2500 grams), miscarriage (\<28 weeks), preterm delivery (\<37 weeks), small for gestational age (SGA), congenital anomaly detected on surface examination, early neonatal mortality (within 7 days of birth)
Maternal Adherence to the Prophylactic Regimen	Adherence of study medication taken at home will be documented from the date of randomization until the time of delivery, assessed up to 42 weeks.	Directly observed therapy (DOT) in clinic for the 1st dose of study medication. Self-report and pill count will be used to assess adherence and maternal tolerability for study medications taken at home from the time of enrollment until delivery. At each follow up visit and at delivery, participants will complete a medication adherence survey. They will self-report adherence to the 3 day study regimen (AZ or placebo).
Proportion of Participants With Symptomatic Malaria	From the date of randomization until the time of delivery, assessed up to 42 weeks.	Fever and positive malaria test (rapid diagnostic test) at routine visits or sick call visits or maternal report of malaria diagnosis.
Proportion With Placental Malaria	At delivery	Placentas will be collected on a subset of women and impression smear will be used to assess for malaria infection
Proportion With Maternal Anemia and Severe Maternal Anemia	At the end of pregnancy (>35 weeks) or at delivery	anemia defined as hemoglobin \<11 g/dL, severe anemia defined as hemoglobin \<7 g/dL.
GBS Colonization	at or near term or at delivery	anogenital GBS colonization detected by NAAT (PCR)
Composite STI Measure (Including All STI Tests)	After 35 weeks GA or at delivery	Proportion of women with GC/CT (by NAAT), syphilis (by serology), Mycoplasma genitalium (NAAT).

Trial Locations

Locations (1)

University of Alabama at Birmingham; 🇺🇸 Birmingham, Alabama, United States