Clinical trial

Repurposing Clinically Approved Drugs for Yaws With an Insight Into the Cutaneous Ulcer Disease Syndrome (Trep-AByaws)

Name
Trep-AByaws
Description
The goal of this clinical trial is to test the non inferiority of linezolid compared with azithromycin as a treatment for yaws . The main questions it aims to answer are: can linezolid cure active yaws, and can linezolid cure latent yaws. Participants with serologically confirmed yaws will be randomized to receive linezolid (experimental) or azithromycin (control group) treatment and followed up to assess clinical resolution.
Trial arms
Trial start
2023-03-14
Estimated PCD
2024-06-20
Trial end
2024-12-01
Status
Active (not recruiting)
Phase
Early phase I
Treatment
Linezolid Oral Tablet
Oral tablet of linezolid 10mg/kg every 8 hours for 7 days.
Arms:
Linezolid
Other names:
Zyvox, Zyvoxid
Azithromycin Oral Tablet
Oral tablet of azithromycin 30mg/kg maximum 2gr single dose.
Arms:
Azithromycin
Other names:
Zithromax
Size
465
Primary endpoint
Clinical resolution
4 weeks after treatment
Serological cure
24 weeks after treatment
Serological cure
48 weeks after treatment
Relapse
24 weeks after treatment
Relapse
48 weeks after treatment
Eligibility criteria
Inclusion Criteria: 1. Participants 5-18 years identified during an active case search program at the elementary, primary and secondary schools in the Islands Region. 2. CUD syndrome suspected due to yaws: one or more ulcerative or nodular or papilloma skin lesion of more than 1 cm in diameter. 3. Positive treponemal (T1) and non-treponemal (T2) serology by Chembio dual path platform (DPP) syphilis screen \& confirm assay (DPP test). 4. Accepted and signed informed consent. 5. Ability to comply with the requirements of the study protocol including follow up visits. Exclusion Criteria: 1. Children younger than 5 years old. 2. Clinical late-stage possible yaws: destructive osteitis (rhinopharyngitis gangosa, sabre shins) or gummous nodules. 3. Known allergy to LZD or AZI antibiotics. 4. Pregnant or breastfeeding women. 5. Refusal at ward level or village chief (for village inclusion), or refusal of individual or guardian (for individual inclusion). 6. Have taken any antibiotics with potential activity against TPE within the last 7 days prior to randomization (i.e., beta lactams, cephalosporines, macrolides, tetracyclines). 7. Uncontrolled hypertension, pheochromocytoma, thyrotoxicosis, carcinoid syndrome, bipolar disorder, incapacitating psycho-affective disturbance, acute confusional state. 8. Renal function impairment requiring hemodialysis. 9. Current treatment with any drugs likely to interact with the study medication 10. Symptomatic concomitant infection requiring antibiotic treatment potentially active against TPE. 11. Having received treatment for yaws in the last 6 months. 12. Patients who are unable to take oral medication or having a gastrointestinal disease likely to interfere with drug absorption (including malnutrition and stomach flu).
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Open-label, non inferiority, two arms and randomized clinical trial. Eligible patients will be randomized (1:1) to receive Linezolid (experimental arm) or Azithromycin (control arm).', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'maskingDescription': 'Investigator will not be present for treatment nor for outcome assessment, and data analysis (statistics) will be blinded.', 'whoMasked': ['INVESTIGATOR']}}, 'enrollmentInfo': {'count': 465, 'type': 'ACTUAL'}}
Updated at
2024-06-11

1 organization

2 products

2 indications

Product
Linezolid
Indication
Yaws
Indication
Skin Ulcer