- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT00978068
HIV Protease Inhibitors for the Prevention of Malaria in Ugandan Children (PROMOTE-PEDS)
A Randomized Open Label Trial of HIV Protease Inhibitors for the Prevention of Malaria in HIV-Infected Children
Przegląd badań
Status
Warunki
Szczegółowy opis
This is an open label, single site, randomized clinical trial comparing PI-based ART to NNRTI-based ART for the prevention of malaria in HIV-infected children. The two ART drug regimens that will be used include: Treatment arm 1. LPV/r + 2 NRTIs and Treatment arm 2. NVP or EFV + 2 NRTIs. The study is designed to test the hypothesis that children receiving a PI-based ART regimen will have lower the incidence of malaria compared to children receiving an NNRTI- based ART regimen. The primary study endpoint of the study is malaria incidence.
The study site will be the Tororo District Hospital campus situated in Eastern Uganda, an area of high malaria transmission. Using convenience sampling, 300 HIV-infected children identified from the Tororo community aged 2 months to <11 years either eligible for ART-initiation or already receiving a first line ART regimen with HIV RNA<400 copies/ml will be evaluated for enrollment.
Eligible children will be randomized at enrollment to receive either a PI- based or an NNRTI-based ART regimen. At enrollment, all study participants will receive a long lasting ITN as part of a basic care package including a safe water vessel and multivitamins and given TS chemoprophylaxis, as per current standard of care for HIV-infected children in Uganda. On the day of ART initiation, patients will be counseled about the importance of adherence to ART and possible ART related toxicities. After 2 weeks, patients will be seen to assess adherence and toxicity to study medications by interview and clinical examination. Apart from this visit at week 2, patients will be seen at 4 week intervals timed from ART-initiation. Assessment of adherence will also be done for TS prophylaxis, ITN use and ART. Assessment of adherence to ART will be done by self report of missed doses and pill counts.
Participants will receive all routine and acute medical care at a designated study clinic open 7 days a week from 8 a.m. to 5 p.m. Parents/guardians will be asked to bring their child to the study clinic for all medical care. If after hours, they will be instructed to bring them to Tororo District Hospital premises (where the study clinic is located) and request that the study physician on-call be contacted. They will be followed for at least 24 months and up to 3 years. They will be seen monthly for routine assessments with laboratory evaluations done at every 3 months. At these visits, the study protocol will be reinforced with discussion regarding the need to come to the study clinic promptly upon the onset of any illness and to avoid use of outside medications. Study participants will also be followed closely for adverse events potentially due to study drugs and for malaria and HIV treatment outcomes. During the follow-up period, all patients presenting to the clinic with a new episode of fever will undergo standard evaluation (history, physical examination) and Giemsa-stained blood smear for the diagnosis of malaria.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Faza 3
Kontakty i lokalizacje
Lokalizacje studiów
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Tororo, Uganda
- IDRC - Tororo Research Clinic
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion criteria:
- Age 2 months to < 11 years
- Confirmed HIV diagnosis. i. Children > 18 months: Documentation of HIV status must come from two assays. Assays include DNA PCR, HIV RNA, Western blot, or rapid HIV antibody test ii. Children < 18 months: Documentation will be DNA PCR confirmation only along with documentation of testing from the referral entity
- ART-naïve patients eligible for ART initiation per WHO/Uganda guidelines (see Table 1) or Patients receiving first line ART regimen with NNRTI +2 NRTI with at least one HIV RNA <400 copies/ml within the past 6 months
- Agreement to come to the study clinic for any febrile episode or other illness
- Agreement to avoid medications administered outside study protocol
- Provision of informed consent by parent/guardian and agreement to have child's care at the clinical site
- Lives within 50 km of study site
Exclusion criteria:
- ART-naïve children: children or their mothers that have received any dose of Nevirapine in the past 24 months
- Active medical problem requiring in-patient evaluation at the time of screening or enrollment
- History of cardiac conduction disorder or known significant cardiac structural defect
- Children receiving any disallowed medications (see section 4.3)
Moderate, Severe or Life-threatening (Grade 2, 3, or 4) AST or ALT found within 4 weeks prior to enrollment:
- AST: >113U/L (>2.5xULN)
- ALT: >113U/L (>2.5xULN)
Life-threatening (Grade 4) screening laboratory value found within 4 weeks prior to enrollment for the following:
- Absolute neutrophil count: <500 mm3
- Hemoglobin: <6.5 g/dL
- Creatinine: >3.5xULN
- Platelets: <25,000/mm3
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Zapobieganie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Aktywny komparator: Lopinavir/ritonavir (LPV/r) +2 NRTI
Lopinavir/ritonavir (LPV/r) +2 nucleoside reverse transcriptase inhibitor (NRTI)
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Inne nazwy:
The same NRTI choice strategy will be used for both arms.
Lamivudine will be used with all children.
The second NRTI will be zidovudine unless the participant has a hemoglobin < 8 gm/dL, in which case it will be Abacavir.
Stavudine will be used in the event that a participant is unable to take Abacavir for safety or other reasons.
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Aktywny komparator: Nevirapine (NVP) or Efavirenz (EFV) +2 NRTI
Nevirapine (NVP) or Efavirenz (EFV) +2 nucleoside reverse transcriptase inhibitor (NRTI)
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The same NRTI choice strategy will be used for both arms.
Lamivudine will be used with all children.
The second NRTI will be zidovudine unless the participant has a hemoglobin < 8 gm/dL, in which case it will be Abacavir.
Stavudine will be used in the event that a participant is unable to take Abacavir for safety or other reasons.
NVP will be used for children < 3 years of age
EFV for children ≥3 years of age
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Ramy czasowe |
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Incidence-density of Malaria Defined as the Number of Incident Episodes of Malaria Per Time at Risk.
Ramy czasowe: Time from randomization to at least 24 months of follow up or until end of the study
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Time from randomization to at least 24 months of follow up or until end of the study
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Percentage of Uncomplicated Malaria Episodes With Accompanying Adverse Events That Occurred in the 28 Days Following Antimalarial Therapy
Ramy czasowe: 28 days after antimalarial therapy
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The rates of adverse events, defined as severity grade 2 or higher that are possibly, probably or definitely related to study drugs over the course of the 28-day period after antimalarial therapy with artemether-lumefantrine (AL).
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28 days after antimalarial therapy
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Incidence-density of Malaria Defined as the Number of Incident Episodes of Complicated Malaria Per Time at Risk.
Ramy czasowe: Time from randomization to at least 24 months of follow up or until end of the study
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Time from randomization to at least 24 months of follow up or until end of the study
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Estimates of the 6-month Risk of a First Episode of Malaria
Ramy czasowe: Enrollment to 6 months follow up
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To assess the effect of ART independently of potential interactions with antimalarial therapy after treatment for malaria, we compared the two groups with respect to the time to the first episode of malaria.
Cumulative risk was estimated using the Kaplan-Meier product-limit formula.
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Enrollment to 6 months follow up
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28-day Risk of Recurrent Parasitemia
Ramy czasowe: 28 days after antimalarial therapy
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To assess the effect of potential interactions between ART and artemether-lumefantrine, the risks of recurrent parasitemia at 28 days were compared between the two groups.
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28 days after antimalarial therapy
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63-day Risk of Recurrent Malaria
Ramy czasowe: 28 days after antimalarial therapy
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To assess the effect of potential interactions between ART and artemether-lumefantrine, the risks of recurrent malaria at 63 days were compared between the two groups.
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28 days after antimalarial therapy
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Współpracownicy i badacze
Współpracownicy
Śledczy
- Główny śledczy: Grant Dorsey, MD, PhD, University of California, San Francisco
- Dyrektor Studium: Diane V Havlir, MD, University of California, San Francisco
- Główny śledczy: Moses R Kamya MBChB, MMed, MPH, Makerere University
- Główny śledczy: Ted Ruel, MD, University of California, San Francisco
- Główny śledczy: Jane Achan, MBChB, MPed, Makerere University
Publikacje i pomocne linki
Publikacje ogólne
- Achan J, Kakuru A, Ikilezi G, Ruel T, Clark TD, Nsanzabana C, Charlebois E, Aweeka F, Dorsey G, Rosenthal PJ, Havlir D, Kamya MR. Antiretroviral agents and prevention of malaria in HIV-infected Ugandan children. N Engl J Med. 2012 Nov 29;367(22):2110-8. doi: 10.1056/NEJMoa1200501.
- Ikilezi G, Achan J, Kakuru A, Ruel T, Charlebois E, Clark TD, Rosenthal PJ, Havlir D, Kamya MR, Dorsey G. Prevalence of asymptomatic parasitemia and gametocytemia among HIV-infected Ugandan children randomized to receive different antiretroviral therapies. Am J Trop Med Hyg. 2013 Apr;88(4):744-6. doi: 10.4269/ajtmh.12-0658. Epub 2013 Jan 28.
- Nsanzabana C, Rosenthal PJ. In vitro activity of antiretroviral drugs against Plasmodium falciparum. Antimicrob Agents Chemother. 2011 Nov;55(11):5073-7. doi: 10.1128/AAC.05130-11. Epub 2011 Aug 29.
- Ruel TD, Kakuru A, Ikilezi G, Mwangwa F, Dorsey G, Rosenthal PJ, Charlebois E, Havlir D, Kamya M, Achan J. Virologic and immunologic outcomes of HIV-infected Ugandan children randomized to lopinavir/ritonavir or nonnucleoside reverse transcriptase inhibitor therapy. J Acquir Immune Defic Syndr. 2014 Apr 15;65(5):535-41. doi: 10.1097/QAI.0000000000000071.
- Kakuru A, Achan J, Muhindo MK, Ikilezi G, Arinaitwe E, Mwangwa F, Ruel T, Clark TD, Charlebois E, Rosenthal PJ, Havlir D, Kamya MR, Tappero JW, Dorsey G. Artemisinin-based combination therapies are efficacious and safe for treatment of uncomplicated malaria in HIV-infected Ugandan children. Clin Infect Dis. 2014 Aug 1;59(3):446-53. doi: 10.1093/cid/ciu286. Epub 2014 Apr 23.
- Bartelink IH, Savic RM, Dorsey G, Ruel T, Gingrich D, Scherpbier HJ, Capparelli E, Jullien V, Young SL, Achan J, Plenty A, Charlebois E, Kamya M, Havlir D, Aweeka F. The effect of malnutrition on the pharmacokinetics and virologic outcomes of lopinavir, efavirenz and nevirapine in food insecure HIV-infected children in Tororo, Uganda. Pediatr Infect Dis J. 2015 Mar;34(3):e63-70. doi: 10.1097/INF.0000000000000603.
- Achan J, Kakuru A, Ikilezi G, Mwangwa F, Plenty A, Charlebois E, Young S, Havlir D, Kamya M, Ruel T. Growth Recovery Among HIV-infected Children Randomized to Lopinavir/Ritonavir or NNRTI-based Antiretroviral Therapy. Pediatr Infect Dis J. 2016 Dec;35(12):1329-1332. doi: 10.1097/INF.0000000000001318.
- Bangirana P, Ruel TD, Boivin MJ, Pillai SK, Giron LB, Sikorskii A, Banik A, Achan J. Absence of neurocognitive disadvantage associated with paediatric HIV subtype A infection in children on antiretroviral therapy. J Int AIDS Soc. 2017 Oct;20(2):e25015. doi: 10.1002/jia2.25015.
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Infekcje
- Choroby przenoszone przez wektory
- Choroby pasożytnicze
- Infekcje pierwotniakowe
- Malaria
- Molekularne mechanizmy działania farmakologicznego
- Środki przeciwinfekcyjne
- Środki przeciwwirusowe
- Inhibitory syntezy kwasów nukleinowych
- Inhibitory enzymów
- Agenci przeciw HIV
- Środki przeciwretrowirusowe
- Inhibitory proteazy
- Inhibitory cytochromu P-450 CYP3A
- Inhibitory enzymów cytochromu P-450
- Induktory enzymów cytochromu P-450
- Induktory cytochromu P-450 CYP3A
- Inhibitory proteazy HIV
- Inhibitory wirusowych proteaz
- Induktory cytochromu P-450 CYP2B6
- Inhibitory cytochromu P-450 CYP2C9
- Inhibitory cytochromu P-450 CYP2C19
- Newirapina
- Rytonawir
- Lopinawir
- Inhibitory odwrotnej transkryptazy
- Efawirenz
Inne numery identyfikacyjne badania
- H5747-34097
- NIH PO1 HD059454
- 2009-114 (Inny identyfikator: Makerere Univ Fac of Med Research and Ethics Committee)
- HS-620 (Inny identyfikator: Uganda National Council for Science and Tech)
- 551/ESR/NDA/DID-08/09 (Inny identyfikator: Uganda National Drug Authority)
- H5741-34097 and 10-00991 (Inny identyfikator: UCSF Committee on Human Research)
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