HIV Infections
Conditions
Keywords
Treatment Naive, MTCT, HIV Seronegativity
Brief summary
Anti-HIV drug regimens have dramatically improved the rates of prevention of mother-to-child transmission (MTCT) of HIV in developed countries. However, little is known of the effectiveness of such regimens in developing countries, such as Botswana. This study will determine whether Trizivir (TZV), a single pill containing abacavir sulfate, lamivudine, and zidovudine (ABC/3TC/ZDV), or lopinavir/ritonavir (LPV/r) and lamivudine/zidovudine (3TC/ZDV) is more effective in reducing HIV-1 viral load and preventing MTCT among HIV infected pregnant women in Botswana.
Detailed description
While perinatal HIV infection has become rare in developed countries through the use of highly active antiretroviral therapy (HAART), it remains a serious problem in developing countries. Botswana has a population of approximately 1.7 million; the prevalence of HIV in Botswana is about 37.4%. In the developed world, HAART has revolutionized the prevention of MTCT among nonbreastfed infants. This trial will compare the effectiveness of a protease inhibitor (PI)-based regimen versus a triple nucleoside reverse transcriptase inhibitor (NRTI)-based regimen in preventing MTCT of HIV. This study will last up to 24 months for mothers and their children. Participants will be stratified based on their CD4 count at screening. Women with CD4 counts of 200 cells/mm3 or more will be in one of two treatment groups and will be randomly assigned to receive either TZV twice daily or LPV/RTV and 3TC/ZDV twice daily. Once in labor, treatment group participants will continue to take their assigned HAART regimen and will also be given additional ZDV. Women with CD4 counts less than 200 cells/mm3 will receive nevirapine (NVP) once daily for the first 14 days, then twice daily, and 3TC/ZDV twice daily; these women will be in the observational group. Shortly after birth, infants will receive single-dose NVP. A 1-month supply of ZDV will be provided to the mother to administer daily to her child. Mothers will stop HAART at 6 months postpartum or when they stop breastfeeding, whichever occurs earlier. A clinical evaluation, blood collection, and HIV prevention counseling will occur at all maternal visits. An obstetrical exam and physical exam will occur at selected visits. Women will provide at least four samples of breast milk during the first 5 months postpartum. For infants, a clinical evaluation will occur at every visit, and a physical exam and blood collection will occur at selected visits.
Interventions
300 mg abacavir sulfate/150 mg lamivudine/300 mg zidovudine tablet taken orally twice daily
150 mg lamivudine/300 mg zidovudine tablet taken orally twice daily
400 mg lopinavir/100 mg ritonavir tablet taken orally twice daily
200 mg tablet taken orally daily for the first 14 days before receiving 200 mg tablet taken orally twice daily
Sponsors
Study design
Eligibility
Inclusion criteria
for Mothers: * HIV-infected * At least at 26th week of pregnancy (treatment group) or 18th week of pregnancy (observational group) but not beyond the 34th week of pregnancy * Able to complete study visits until at least 6 months postpartum * Citizen of Botswana
Exclusion criteria
for Mothers: * Taken ARVs for more than 1 week, other than ZDV, during current or prior pregnancy. Women who have received single-dose NVP in a prior pregnancy are not excluded. * Certain abnormal laboratory values * Plan to formula feed * Known fetal abnormalities that suggest the fetus will not survive to 6 months of gestational age * Known allergy or medical contraindication to any of the study drugs * Require certain medications * Previous participation in the Prevention of Milk-Borne Transmission of HIV-1C in Botswana (Mashi) study * Currently incarcerated
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Virologic Suppression | Throughout study, including breastfeeding, assessed up to 24 months | Suppression of the plasma HIV-1 RNA level to less than 400 copies per milliliter |
| Number of HIV+ Infants | Throughout study, including breastfeeding, assessed up to 24 months | Number of infants with HIV-positive status |
Countries
Botswana
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| TZV Arm Participants in Arm 1A will have CD4 counts of 200 cells/mm3 or more and will receive TZV twice daily. Once in labor, these participants will continue to take TZV twice daily and will also be given additional ZDV.
Trizivir: 300 mg abacavir sulfate/150 mg lamivudine/300 mg zidovudine tablet taken orally twice daily | 285 |
| Kaletra Arm Participants in Arm 1B will have CD4 counts of 200 cells/mm3 or more and will receive LPV/RTV and 3TC/ZDV twice daily. Once in labor, these participants will continue to take TZV twice daily and will also be given additional ZDV.
Lamivudine/Zidovudine: 150 mg lamivudine/300 mg zidovudine tablet taken orally twice daily
Lopinavir/Ritonavir: 400 mg lopinavir/100 mg ritonavir tablet taken orally twice daily | 275 |
| NVP Arm Participants in Arm 2 will have CD4 counts less than 200 cells/mm3 and will receive NVP once daily for the first 14 days, then twice daily, and 3TC/ZDV twice daily; these women will be in the observational group.
Nevirapine: 200 mg tablet taken orally daily for the first 14 days before receiving 200 mg tablet taken orally twice daily | 170 |
| Total | 730 |
Baseline characteristics
| Characteristic | TZV Arm | Kaletra Arm | NVP Arm | Total |
|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 285 Participants | 275 Participants | 170 Participants | 730 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 285 Participants | 275 Participants | 170 Participants | 730 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Region of Enrollment Botswana | 285 participants | 275 participants | 170 participants | 730 participants |
| Sex: Female, Male Female | 285 Participants | 275 Participants | 170 Participants | 730 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 1 / 285 | 0 / 275 | 3 / 170 |
| other Total, other adverse events | 0 / 285 | 0 / 275 | 0 / 170 |
| serious Total, serious adverse events | 42 / 285 | 32 / 275 | 48 / 170 |
Outcome results
Number of HIV+ Infants
Number of infants with HIV-positive status
Time frame: Throughout study, including breastfeeding, assessed up to 24 months
Population: Analysis is based on actual number of available patients, and may not perfectly match the Patient Flow module.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| TZV Arm | Number of HIV+ Infants | 6 Infants |
| Kaletra Arm | Number of HIV+ Infants | 1 Infants |
| NVP Arm | Number of HIV+ Infants | 1 Infants |
Number of Participants With Virologic Suppression
Suppression of the plasma HIV-1 RNA level to less than 400 copies per milliliter
Time frame: Throughout study, including breastfeeding, assessed up to 24 months
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| TZV Arm | Number of Participants With Virologic Suppression | 274 Participants |
| Kaletra Arm | Number of Participants With Virologic Suppression | 256 Participants |
| NVP Arm | Number of Participants With Virologic Suppression | 160 Participants |