Ozmosi | Nifurtimox Drug Profile
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Nifurtimox

Pronounced as: nye-FUR-tih-mox

Alternative Names: nifurtimox, lampit
Clinical Status: Active
Latest Update: 2024-08-06
Latest Update Note: Clinical Trial Update

Product Description

Nifurtimox has been used to treat Chagas disease for 40 years, but tolerance and safety data in adults are scarce. Nifurtimox is poorly tolerated among adults with chronic Chagas disease, resulting in a low treatment completion rate. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/20932171/)

Mechanisms of Action: DNA Cleaver

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Approved

Approved Countries: Argentina | Chile | Colombia | Mexico | Peru | United Kingdom | United States

Approved Indications: None

Known Adverse Events: None

Company: Bayer
Company Location:
Company Founding Year: 1863
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Nifurtimox

Countries in Clinic: China

Active Clinical Trial Count: 2

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Brain Stem Cancer|Breast Cancer|Central Nervous System Cancer|Glioma|Lung Cancer|Medulloblastoma|Melanoma|Neuroblastoma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

CTR20220156

CTR20220156

P1

Recruiting

Glioma|Lung Cancer|Medulloblastoma|Brain Stem Cancer|Melanoma|Breast Cancer|Central Nervous System Cancer

None

2025-04-29

Patient Enrollment

CTR20190136

CTR20190136

P1

Recruiting

Neuroblastoma

None

2025-04-29

Patient Enrollment|Treatments