CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 330 enrolled
Drug / intervention
Nifurtimox (Lampit, BAYA2502) +1 moredrug
Likely dose
Nifurtimox (Lampit, BAYA2502) 20 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02625974
NCT02625974Phase 3Completed

Prospective, Historically Controlled Study to Evaluate the Efficacy and Safety of a New Pediatric Formulation of Nifurtimox in Children Aged 0 to 17 Years With Chagas' Disease

Bayer·interventional·Posted Dec 9, 2015·Updated Aug 19, 2024

In Brief

A Phase 3 clinical trial evaluating Nifurtimox (Lampit, BAYA2502) and Placebo for Chagas Disease. Completed, enrolled 330 participants across 25 sites in 3 countries.

Detailed Summary

Researchers are looking for a better way to treat children who have an infectious disease caused by the parasite Trypanosoma cruzi (Chagas' disease). Chagas'disease is an inflammatory, infectious disease caused by the parasite Trypanosoma cruzi. This parasite is mainly spread by insects called triatomine bug. If Chagas' disease is left untreated, it can later cause serious heart and digestive problems. The study treatment nifurtimox has been used for more than 50 years to treat Chagas' disease. When used early after infection, it kills the parasite. In people who have long-term Chagas' disease, it's no longer possible to kill the parasite. However, nifurtimox may help slow the progression of the disease and its most serious complications. Nifurtimox was developed for use in adults only, but has also been used in children (off-label) for over 40 years. Currently it is available for doctors to give to adults and to children. However, there are not enough data about nifurtimox in children. The main purpose of this study is to learn how well nifurtimox works in children aged 8 months to less than 18 years with Chagas' disease. To answer this, the researchers will compare the amount of antibodies against the parasite Trypanosoma cruzi in the serum (fluid from blood without the clotting factors) between children treated with nifurtimox for 60 days with untreated children from the past (control group): * 12 months and * 4 years after the end of treatment. The data for the control group will come from 2 previous studies conducted in children.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChagas Disease
CountriesArgentina, Bolivia, Colombia
Collaborators--

Timeline

Phase 3CompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 9, 2015
Enrollment StartJan 27, 2016
Primary CompletionJul 25, 2018
Study CompletionAug 10, 2021
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 10.6 years ago

Interventions

Nifurtimox (Lampit, BAYA2502)drug

For pediatric participants with body weight ≤ 40 kg: dosage 10 to 20 mg/kg/day in three divided doses. For pediatric participants with body weight \> 40 kg: 8 - 10 mg/kg/day in three divided doses. 60 days or 30 days of nifurtimox treatment

Placebodrug

Matching placebo