Daily Trimethoprim-sulfamethoxazole or Weekly Chloroquine Among Adults on ART in Malawi

This is a randomized, controlled, open-label, phase III trial of standard of care TS prophylaxis and CQ prophylaxis compared to no prophylaxis in adults receiving ART. Adults who have been receiving ART for at least six months with a good clinical response and provide informed consent and fulfill the eligibility criteria will be randomized to one of three arms: (1) to continue standard of care trimethoprim-sulfamethoxazole (TS) prophylaxis, (2) discontinue standard of care TS prophylaxis and begin weekly CQ prophylaxis or (3) discontinue standard of care TS prophylaxis. Participants will be asked to return to the research clinic every four weeks for the first 24 weeks then every 12 weeks thereafter, and any time they are ill to facilitate both active and passive follow-up of the study endpoints. Participation will last for 32 to approximately 66 months. Participants who develop a WHO clinical stage 3 or 4 illness, experience a sustained decline in their CD4 count below 200 cells/mm3, or who experience ART failure will be placed on standard of care TS prophylaxis. Those with confirmed ART failure will be evaluated for second-line therapy according to the Malawi Ministry of Health guidelines.

The study population will include up to 1500 Malawian adults aged 18 years or older living with HIV in or near Blantyre or Zomba, Malawi, Central Africa who have been receiving antiretroviral therapy for at least 6 months with good clinical response to ART, have an undetectable HIV viral load and a CD4 count >250/mm3.

Inclusion criteria

• Age 18 years or older
• Documented HIV-1 infection
• Initiation of ART through a government-sponsored ART program at least six months prior
• Undetectable HIV viral load (< 400 copies/mL)
• CD4 count > 250/mm3
• TS prophylaxis prescribed for at least the previous 2 months
• Intention to remain in the study area until the end of the study period
• Informed consent from participant
• Female study volunteers of reproductive potential must have a negative urine pregnancy test performed within 20 days before randomization.
• Female study volunteers of reproductive potential who participate in sexual activity that could lead to pregnancy must use contraception (male or female condoms, diaphragm or cervical cap with spermicide, intrauterine device, or hormone-based contraceptive) while receiving their assigned study drug and for one month after stopping the medications.

Exclusion criteria

• Severe acute illness (defined as requiring hospitalization at the time of screening or other conditions such as laboratory abnormalities as determined by the investigators)
• Chronic treatment (requiring therapy for > 14 days) or secondary prophylaxis (for toxoplasmosis, Pneumocystis pneumonia, or tuberculosis for example) with any drug with antimalarial or antibacterial activity
• History of hypersensitivity to antifolate drugs or CQ
• Laboratory exclusion criteria
• Hemoglobin < 8.0 gm/dL
• Platelet count < 50,000/mm3
• Absolute granulocyte count < 500/mm3
• Serum alanine aminotransferase (ALT) concentration > 210 U/L for men, >160 U/L for women
• Serum creatinine concentration > 3.3mg/dl (291.7µmol/L) for men, and > 2.7mg/dl (238.7µmol/L) for women)
• History of visual field or retinal changes
• History of preexisting auditory damage
• History of porphyria
• History of psoriasis
• History of liver disease
• History of seizure disorder
• History of glucose-6-phosphate dehydrogenase (G6PD) deficiency
• History of ECG and cardiac conduction abnormality or cardiomyopathy
• History of myopathy