Comparing PI-Based to a nNRTI-based ART for Clearance of Plasmodium Falciparum Parasitemia in HIV-Infected

Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections

Status and phase: Completed; Phase 2; Phase 1

Conditions: Pf Subclinical Parasitemia; HIV-1 Infection

Treatments: Drug: Lopinavir/ritonavir; Drug: Emtricitabine/tenofovir disoproxil fumarate; Drug: Efavirenz; Drug: Nevirapine; Drug: Trimethoprim/sulfamethoxazole

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT01632891

1U01AI068636 (U.S. NIH Grant/Contract)

ACTG A5297

Details and patient eligibility

About

The purpose of this study was to see if antiretroviral therapy (ART) is safe and works at getting rid of malaria in blood and to see whether one type of ART is better than another. This study may offer information for further research in looking at whether ART plays a role in the prevention and treatment of malaria.

Full description

A5297 was a Phase I/II, open-label, proof of concept, two-step, two-arm, randomized controlled clinical trial (RCT) to test the superiority of lopinavir/ritonavir (LPV/r)-based antiretroviral therapy (ART) to non-nucleoside reverse transcriptase (nNRTI)-based ART for clearance of Plasmodium falciparum (Pf) subclinical parasitemia (SCP).

The study consisted of two steps. At study Step 1 entry, participants were randomized 1:1 to either LPV/r-based ART or nNRTI-based ART for 15 days. In study Step 2, all participants received nNRTI-based ART and TMP/SMX prophylaxis for 15 days. The total study duration was 30 days.

Study visits occurred every 3 days in Step 1, and every 5 days in Step 2. At each study visit, 2 samples were taken for measurement of parasite density, except day 15 and day 30 at which 3 samples were taken.

Adverse events which occurred after randomization were also recorded. Signs/symptoms and diagnoses were evaluated at each visit, while safety labs (including Hemoglobin, hematocrit, white blood cell count (WBC), differential WBC, platelet count, and absolute neutrophil count (ANC), glucose, electrolytes (sodium, potassium, chloride, bicarbonate), total bilirubin, AST (SGOT), ALT (SGPT), albumin, alkaline phosphatase, and creatinine) were taken at day 15 and day 30, or if indicated at other study visits.

Enrollment: 52 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• HIV-1 infection

• CD4+ count > 200 and < 500 cells/mm^3 obtained within 30 days prior to study entry at a DAIDS-approved laboratory.

• Pf SCP confirmed in a laboratory approved to conduct parasitemia microscopy. Note: Pf SCP defined as meeting all three of the following criteria within 72 hours prior to study entry:

  1. Microscopy confirmed parasitemia (see section 6.3.6 and the A5297 Manual of Procedures [MOPS])

  2. An oral temperature < 37.5°C.

  3. The absence of Grade 2 or greater signs or symptoms thought to be related to clinical malaria including:

     1. headache
     2. malaise or fatigue
     3. abdominal discomfort
     4. muscle or joint pain
     5. fever
     6. chills
     7. perspiration
     8. anorexia
     9. vomiting
     10. other signs or symptoms thought to be related to clinical malaria

• Certain laboratory values obtained within 14 days prior to study entry, as detailed in section 4.1.4 of the protocol.

• Hepatitis B surface antigen (HBsAg) negative within 30 days prior to entry.

• Female study volunteers of reproductive potential have a negative serum or urine pregnancy test performed within 72 hours prior to entry.

• All study volunteers agree not to participate in a conception process (eg, active attempt to become pregnant or to impregnate, sperm donation, in vitro fertilization) for study duration. If participating in sexual activity that could lead to pregnancy, must agree to use two reliable forms of contraceptive simultaneously while receiving protocol-specified medications. One form of contraceptive must be a barrier method if a participant receives EFV. Participants must agree to continue the use of two contraceptives for 6 months after stopping EFV and 6 weeks after stopping all other protocol-specified medications.

• Study volunteers who are not of reproductive potential are eligible without requiring the use of a contraceptive.

• Ability and willingness of participant or legal guardian/representative to provide informed consent.

• Willing and able to return to the clinic twice to three times a day for study visits.

Exclusion criteria

Step 1: Exclusion Criteria

• Previous history or current use of ART.
• Single dose NVP or dual therapies used for Prevention of mother-to-child transmission (PMTCT) within 2 years prior to entry.
• Use of any medication with antimalarial activity, including TMP/SMX (see list of prohibited medications in the A5297 Manual of Procedures (MOPS)), within 14 days prior to study entry.
• Confirmed or clinically suspected OIs (including but not limited to tuberculosis, clinical malaria, PCP), or other pulmonary or gastrointestinal infections for which potential participants did not complete treatment more than 30 days prior to enrollment or have signs and symptoms during screening.
• Breastfeeding.
• Known allergy/sensitivity or any hypersensitivity to components of study drugs or their formulation.
• Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
• Serious illness requiring systemic treatment and/or hospitalization within 30 days prior to entry.
• Results suggestive of active pulmonary disease from a chest x-ray performed within 30 days prior to study entry.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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52 participants in 2 patient groups

LPV/r-based ART

Experimental group

Description:

Participants were prescribed to LPV/r-based antiretroviral therapy (ART) for 15 days, which includes lopinavir/ritonavir plus emtricitabine/tenofovir disoproxil fumarate; followed by an nNRTI-based ART, which includes efavirenz, nevirapine, plus emtricitabine/tenofovir disoproxil fumarate, and Trimethoprim/sulfamethoxazole prophylaxis to take from day 16 through day 30.

Treatment:

Drug: Trimethoprim/sulfamethoxazole

Drug: Nevirapine

Drug: Efavirenz

Drug: Emtricitabine/tenofovir disoproxil fumarate

Drug: Lopinavir/ritonavir

nNRTI-based ART

Experimental group

Description:

Participants were prescribed to nNRTI-based ART for 15 days, which includes efavirenz, nevirapine, plus emtricitabine/tenofovir disoproxil fumarate, followed by an nNRTI-based ART and Trimethoprim/sulfamethoxazole prophylaxis to take from day 16 through day 30.

Treatment:

Drug: Trimethoprim/sulfamethoxazole

Drug: Nevirapine

Drug: Efavirenz

Drug: Emtricitabine/tenofovir disoproxil fumarate