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

• Status: Completed
• Trial end date: 2018-07-31
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to determine if there is a benefit to taking trimethoprim-sulfamethoxazole (TS) as prophylaxis among HIV positive adults who have viral load suppression and a good clinical response on anti-retroviral therapy (ART). If there is a benefit, then is it due to antimalarial or antibacterial properties.

The investigators hypothesize that there will be a long-term benefit on survival and disease control in the context of prophylaxis and that the benefit will largely be attributed to prevention of malaria. The main study hypothesis is that 1)TS and chloroquine (CQ) will decrease the rates of morbidity and mortality among adults after 6 or more months of ART and 2) CQ prophylaxis will be associated with more prolonged viral suppression and higher CD4 cell counts than TS prophylaxis or no prophylaxis.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of Maryland; University of Maryland, Baltimore
• Collaborator: National Institute of Allergy and Infectious Diseases (NIAID)
• Treatments: Chloroquine; Chloroquine diphosphate; Sulfamethoxazole; Trimethoprim; Trimethoprim, Sulfamethoxazole Drug Combination

Criteria

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