Skip to content

Trizivir Vs. Kaletra and Combivir for the Prevention of Mother-to-Child Transmission of HIV

Lopinavir/Ritonavir/Combivir vs. Abacavir/Zidovudine/Lamivudine for Virologic Efficacy and the Prevention of Mother-to-Child HIV Transmission Among Breastfeeding Women With CD4 Counts Greater Than or Equal to 200 Cells/mm3 in Botswana

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00270296
Enrollment
730
Registered
2005-12-26
Start date
2006-06-30
Completion date
2010-09-30
Last updated
2021-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

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

DRUGLamivudine/Zidovudine

150 mg lamivudine/300 mg zidovudine tablet taken orally twice daily

DRUGLopinavir/Ritonavir

400 mg lopinavir/100 mg ritonavir tablet taken orally twice daily

DRUGNevirapine

200 mg tablet taken orally daily for the first 14 days before receiving 200 mg tablet taken orally twice daily

Sponsors

Harvard School of Public Health (HSPH)
CollaboratorOTHER
National Institute of Allergy and Infectious Diseases (NIAID)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

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

MeasureTime frameDescription
Number of Participants With Virologic SuppressionThroughout study, including breastfeeding, assessed up to 24 monthsSuppression of the plasma HIV-1 RNA level to less than 400 copies per milliliter
Number of HIV+ InfantsThroughout study, including breastfeeding, assessed up to 24 monthsNumber of infants with HIV-positive status

Countries

Botswana

Participant flow

Participants by arm

ArmCount
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
Total730

Baseline characteristics

CharacteristicTZV ArmKaletra ArmNVP ArmTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
285 Participants275 Participants170 Participants730 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
285 Participants275 Participants170 Participants730 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants0 Participants
Region of Enrollment
Botswana
285 participants275 participants170 participants730 participants
Sex: Female, Male
Female
285 Participants275 Participants170 Participants730 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
1 / 2850 / 2753 / 170
other
Total, other adverse events
0 / 2850 / 2750 / 170
serious
Total, serious adverse events
42 / 28532 / 27548 / 170

Outcome results

Primary

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.

ArmMeasureValue (NUMBER)
TZV ArmNumber of HIV+ Infants6 Infants
Kaletra ArmNumber of HIV+ Infants1 Infants
NVP ArmNumber of HIV+ Infants1 Infants
Primary

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

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
TZV ArmNumber of Participants With Virologic Suppression274 Participants
Kaletra ArmNumber of Participants With Virologic Suppression256 Participants
NVP ArmNumber of Participants With Virologic Suppression160 Participants

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026