HIV Infection Clinical Trial
— PENTA 13Official title:
Pharmacokinetic Study of Twice Daily vs Once Daily Lamivudine and Abacavir as Part of Combination Antiretroviral Therapy in Children With HIV Infection
| Verified date | November 2013 |
| Source | PENTA Foundation |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United Kingdom: Department of Health |
| Study type | Interventional |
Cross-over 28 week study of the plasma pharmacokinetic profiles of twice daily 3TC (4mg/kg/dose BD) with once daily 3TC (8mg/kg/dose OD) and twice daily ABC (8mg/kg/dose BD) with daily ABC (16mg/kg/dose OD) where one or both drugs are being taken as part of combination antiretroviral therapy.
| Status | Completed |
| Enrollment | 19 |
| Est. completion date | March 2004 |
| Est. primary completion date | February 2004 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 2 Years to 13 Years |
| Eligibility |
Inclusion Criteria: - Children with definitive HIV infection - Age > 2 and < 13 years - Currently on combination ART including 3TC and / or ABC, for at least 6 months, with stable CD4 cell count and HIV RNA viral load and expected to stay on this regimen for at least a further 3 months. Exclusion Criteria: - • Intercurrent illness - Receiving concomitant therapy except prophylaxis against Pneumocystis carinii pneumonia (PCP) - Abnormal renal or liver function (grade 3 or above) |
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Great Ormond Street Hospital | London | |
| United Kingdom | St. Mary's Hospital | London |
| Lead Sponsor | Collaborator |
|---|---|
| PENTA Foundation |
United Kingdom,
Bergshoeff A, Burger D, Verweij C, Farrelly L, Flynn J, Le Prevost M, Walker S, Novelli V, Lyall H, Khoo S, Gibb D; PENTA-13 Study Group. Plasma pharmacokinetics of once- versus twice-daily lamivudine and abacavir: simplification of combination treatment in HIV-1-infected children (PENTA-13). Antivir Ther. 2005;10(2):239-46. — View Citation
LePrevost M, Green H, Flynn J, Head S, Clapson M, Lyall H, Novelli V, Farrelly L, Walker AS, Burger DM, Gibb DM; Pediatric European Network for the Treatment of AIDS 13 Study Group. Adherence and acceptability of once daily Lamivudine and abacavir in human immunodeficiency virus type-1 infected children. Pediatr Infect Dis J. 2006 Jun;25(6):533-7. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | To describe patient and family acceptability of and adherence to once daily compared to twice daily dosing | week -2 and week 24 | No | |
| Primary | Area Under Curve (AUC) of lamivudine after qd and bid dosing | week 0 and Week 4 | No | |
| Primary | Cmin of lamivudine after qd and bid dosing | week 0 and week 4 | No | |
| Primary | Cmax of lamivudine after qd and bid dosing | week 0 and week 4 | No | |
| Primary | AUC of abacavir after qd and bid dosing | week 0 and week 4 | No | |
| Primary | Cmin of abacavir after qd and bid dosing | week 0 and week 4 | No | |
| Primary | Cmax of abacavir after qd and bid dosing | week 0 and week 4 | No | |
| Secondary | To describe trough intracellular levels of 3TC on twice daily and once daily dosage regimens | Week 0 and week 4 | No |
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