Evaluation of Pharmacokinetics and Safety Tolerability of Higher Doses of Rifampic

NCT ID: NCT04437836

Last Updated: 2024-02-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-07-01
• Study Completion Date: 2023-12-31

Brief Summary

Tuberculosis in children is a major public health problem and it contributes 10% of the total TB cases worldwide. TB treatment outcomes in children are challenged by insufficient consideration of the relationships between doses administered, concentrations achieved and eventual desirable and undesirable effects (pharmacodynamics) of TB drugs. Rifampicin is a pivotal TB drug and data from adults suggest that a much higher dose of rifampicin (35 mg/kg instead of 10 mg/kg), resulting in much higher rifampicin exposures in plasma, is safe and tolerable and may provide a higher efficacy. The dose needed in children to achieve the same exposure in plasma is unknown.

Detailed Description

Tuberculosis (TB) in children is a major public health problem . It has a global estimate of >100,000 deaths per year and is included in the top ten causes of mortality in children worldwide. Children contribute 10% of the total TB cases worldwide. More than 75% of the worldwide estimated cases of TB in children occur in the 30 high burden countries, Tanzania being one of them. The enormous burden of pediatric TB in these countries is due to the TB epidemic amongst adults and the simultaneous HIV pandemic and a child less than 14 years of age whether HIV infected or not is at a high risk of developing the disease. Subsequent dissemination of the mycobacterium and progression of the disease is also fast in children.

Knowledge on the efficacy and safety of medicines for children is still very limited and sometimes children are still being treated as small adults. However, adult dosing cannot be logically extrapolated to children according to weight or age because of different pharmacokinetics, i.e. the relationship between doses administered and exposures (drug concentrations) achieved, in children as compared with adults . More specifically, these pharmacokinetic differences occur in the subsequent processes of absorption, distribution, metabolism and elimination of drugs, which are subject to physiological changes due to growth and development in children. Especially in young children, maturation of liver metabolism pathways and renal function are not completed.

In contrast, the pharmacodynamics of a drug, i.e. the relationship between concentrations achieved and eventual response is generally considered similar between adults and children, although differences in drug metabolism between children and adults may lead to differences in susceptibility to some adverse drug reactions. Thus, because of the differences in pharmacokinetics in children with different ages, they should not receive the same drug doses on mg/kg base as adults, and drug dosage selection in children should rather be based upon stages of growth and development. These drug doses should target the exposures that are efficacious in adults.

Conditions

Clinical Trial

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Control arm

Participants will receive standard treatment of rifampicin

Group Type: EXPERIMENTAL

Evaluation of high dose rifampicin in children

Intervention Type: DRUG

Evaluation of severity of adverse event from grade 1 to 5

First High dose

Participants will receive 30mg per kg body weight of rifampicin

Group Type: EXPERIMENTAL

Evaluation of high dose rifampicin in children

Intervention Type: DRUG

Evaluation of severity of adverse event from grade 1 to 5

Second high dose

Particpants will receive 40mg per kg body weight of rifampicin

Group Type: EXPERIMENTAL

Evaluation of high dose rifampicin in children

Intervention Type: DRUG

Evaluation of severity of adverse event from grade 1 to 5

Interventions

Evaluation of high dose rifampicin in children

Evaluation of severity of adverse event from grade 1 to 5

Intervention Type: DRUG

Other Intervention Names

Safety monitoring

Eligibility Criteria

Inclusion Criteria

• Children aged 1 to 14 years with newly diagnosed Tuberculosis

Exclusion Criteria

• Children with elevated liver function
• Children allergic to first line anti-TB drugs

• Minimum Eligible Age: 1 Year
• Maximum Eligible Age: 14 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

European and Developing Countries Clinical Trials Partnership (EDCTP)

OTHER_GOV

Sponsor Role: collaborator

Kilimanjaro Clinical Research Institute

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Kilimanjaro Clinical Research Institute

Moshi, Kilimanjaro, Tanzania

Hydom Hospital

Babati, Manyara Region, Tanzania

Mt. Meru Hospital

Arusha, , Tanzania

Huruma Hospital

Moshi, , Tanzania

Countries

Tanzania

Other Identifiers

TMA2017CDF-1876-HighRif C

Identifier Type: -

Identifier Source: org_study_id