Nitrite Infusion in Children With Malaria
Safety, Feasibility, and Endothelial Effects of Sodium Nitrite Infusion in Children With Falciparum Malaria
Descripción general del estudio
Descripción detallada
This is a Phase I, open-label, dose-escalation study that will enroll up to 24 patients total, using a 3+3 dose escalation design, with 3 to 6 patients per dose level at up to 4 sequential dose levels (0.16, 0.32, 0.64 and 1.28 mcg/kg/minute). At each dose level patients with moderately severe malaria will receive a single 60-minute intravenous infusion of sodium nitrite in 0.9% sodium chloride. Blood pressure and methemoglobin levels will be closely monitored during the infusion and for 24 hours post infusion.
This study will allow a preliminary analysis of the safety of intravenous sodium nitrite in children with moderately severe malaria and is expected to provide preliminary data on its effects on endothelial function. The hypothesis is that sodium nitrite infusion will be safe at low dosage levels. Additionally, since deficiency of nitric oxide is linked to endothelial dysfunction in malaria, there is the hypothesis that sodium nitrite will result in improved markers of endothelial function.
Children are the largest group affected by falciparum malaria. The study population will be male children residing in Tanzania, ages 4-10 years old diagnosed with moderately severe malaria, who have been hospitalized for treatment of their malaria at Hubert Kairuki Medical University in Dar es Salaam, Tanzania. Patients will receive standard anti-malaria and supportive care treatment. The study will enroll up to 24 subjects.
Participants will receive a single intravenous infusion of sodium nitrite diluted in 0.9% sodium chloride. The infusion will be administered over 60 minutes with an infusion pump. Escala-ting doses of sodium nitrite will be administered to patients in 4 dose level cohorts. Patients will be sequentially enrolled starting at the lowest dose level. Individual patients at the same dose level will also be enrolled sequentially, such that the next patient will not receive treatment until completion of a 24- hour safety monitoring period for the prior patient. Dose assign-ment will be based on the order of study enrollment. The maximum tolerated dose (MTD) is the highest dose level wherein ≤ 1 of 6 evaluable patients experiences dose limiting toxicity (DLT). If the MTD is exceeded at the first dose level, then dosing will cease.
Tipo de estudio
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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Dar es Salaam, Tanzania
- Hubert Kairuki Memorial University
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Provision of signed and dated informed consent from parent or legal guardian
- Males, >4 to 10 years of age
- Body weight > 12 kg
Parasitemia with Plasmodium falciparum including:
- Positive rapid diagnostic test result: AND
- >2,500 parasites/microliter by microscopy
Diagnosis of MSM, as follows:
- Clinical syndrome consistent with malaria associated with documented fever (axillary temperature >38C) or reported history of fever in the past 48 hours with no other cause present; AND
- Exhibiting no WHO warning signs or criteria for SM [27]
- A negative G6PD deficiency test (careSTART G6PD quantitative biosensor)
- Requires inpatient parenteral treatment because of inability to tolerate oral therapy
- Hemoglobin > 8 g/dL (subjects with prior blood transfusion will be eligible).
- Systolic blood pressure > 85 mmHg
- Baseline quantitative methemoglobin measurement less than 2%
- Creatinine less than the upper limit of normal
Exclusion Criteria:
- Female gender
- Diagnosis of severe malaria
- Presence of infection, or mixed infection, with non-falciparum strains of malaria
Signs of severe malaria[27], including 1 or more of the following:
- impaired consciousness (Blantyre coma score <3 in children)
- prostration
- multiple convulsions (>2 within 24 hours)
- acidosis (base deficit >8 mEq/L or bicarbonate <15 mmol/L or lactate > 5 mmol/L)
- hypoglycemia (blood glucose < 40 mg/dL or <2.2 mmol/L)
- severe anemia (Hb < 5g/dL )
- renal impairment (serum creatinine >265 uMol/L or 3 mg/dL; or blood urea >20 mmol/L)
- jaundice (bilirubin >50 umol or 3 mg/dL with parasite count >100000/ µL)
- pulmonary edema (including O2sat <92% with RR >30/min)
- circulatory collapse or shock
- significant bleeding
- hyperparasitemia (>10%)
- Presence of concomitant non-malarial infection
- Known G6PD deficiency
- Known chronic illness including renal, cardiac, pulmonary, epilepsy
- History of a reaction to a substance or medication consisting of dyspnea and cyanosis
- History of trauma or bleeding in the 2 weeks prior to presentation
- Clinical impression of disseminated intravascular coagulation
- Subjects treated with parenteral anti-malarial drugs for more than 12 hours
- Current use of drugs with oxidative potential (e.g., nitrates, dapsone, primaquine); or drugs that cause hypotension.
- Known allergic reactions to sodium nitrite injection
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Sodium Nitrite
Single 60-minute intravenous infusion of sodium nitrite in 0.9% sodium chloride at up to 4 sequential dose levels (0.16, 0.32, 0.64 and 1.28 mcg/kg/minute)
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Single 60 minute infusion at 1 of 4 sequential dose levels (0.16, 0.32, 0.64 and 1.28 mcg/kg/minute).
The dose amount will depend on when the participant enters the study
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Safety as measured by number of subjects with at least one adverse event
Periodo de tiempo: 48 hours post infusion
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Adverse events will be assessed according to the NIH's Table for Grading the Severity of Adult and Pediatric Adverse Events.
Events will be numerically graded 1-5; 1 being a mild event and 5 being death
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48 hours post infusion
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Percent change in microvascular function/activation for each of the 4 dosing levels by linear regression
Periodo de tiempo: 48 hours post infusion
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We will assess possible covariate relationships.
A model will be developed that links the pharmacokinetics with the pharmacodynamic measures of endothelial function and activation
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48 hours post infusion
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Anticipado)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- Pro00100364
- R01HL130763 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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