Telacebec in Adults With Multibacillary Leprosy (TEBULA Leprosy Trial) (TEBULA LEPROSY)
A Multicentre, Phase 2, Open-label, Randomised, Standard of Care-controlled and Dose-ranging Clinical Trial, Evaluating Safety and Efficacy of Telacebec in Adults With Multibacillary Leprosy (TEBULA Leprosy Trial)
The goal of this clinical trail is to evaluate whether short-course telacebec-based regimens can induce rapid and measurable reductions in M. leprae viability, potentially establishing the foundation for future shorter, safer, and simplified therapeutic strategies for MB leprosy.
Participants will be randomised into one of the four study arms (A, B, C and D). The arm A is non interventional. For arms B, C, and D, the three-month study drug treatment will be followed by 9 months of MDT, bringing the total treatment time to 12 months. This provision of MDT ensures that the participant has received the recommended standard treatment for leprosy and is primarily for ethics considerations.
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
This is an open-label, randomised, controlled, multicentre phase II clinical trial conducted in Benin, Côte d'Ivoire and Ethiopia to evaluate the bactericidal efficacy of telacebec-based regimens in the treatment of multibacillary (MB) leprosy, with safety and tolerability as secondary objectives.
Participants who meet entry criteria and give consent will be randomised into four parallel groups: one control group (Group A) receiving standard WHO multidrug therapy (MDT); two investigational groups (Groups B and C) receiving telacebec monotherapy at two different dose levels; and one investigational group (Group D) receiving telacebec in combination with rifampicin. Upon completion of the assigned telacebec-based regimen, participants in Groups B, C, and D will subsequently receive standard WHO MDT.
Follow-up will be at least 12 months for all study arms; however, with the support of national programmes, patients may be followed for up to five years where possible.
Every fortnightly visit during the first three months (during which participants are taking study drugs) needs to be performed on the appointment day (±2 days). During post-IP treatment, once participants are on regular WHO MB-MDT, they are followed up on a monthly basis (-3/+2 days window). During the post-MDT period, they are followed up on a 3-monthly basis (±14 days window). The monthly dose of study medication must be taken as directly observed treatment (DOT) on the day of the visit. The Day 1 of the monthly WHO MB-MDT must also be taken as DOT.
The TEP is composed of clinicians experienced in the clinical management of leprosy, independent of the trial sites, and will provide assistance in reviewing the clinical response of participants included in the clinical trial. During the clinical follow-up, pictures of the lesions are taken systematically at every scheduled visit to document clinical evolution, identified with a code guaranteeing patient and treatment anonymity. After Day 84, pictures will be sent separately to each member of the TEP blinded to treatment allocation. The Technical Expert Panel (TEP) will give an independent assessment classifying each participant as showing clear improvement, moderate improvement, or no improvement.
At least three assessments from the TEP need to be collected for the decision. The decision will be taken by simple majority. If 4 out of 5 members provide an assessment and the decision is divided, a reserve list TEP member will be contacted.
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Roch Christian JOHNSON, Medical Doctor, Phd, HDR
- Número de teléfono: +229(01)96221132
- Correo electrónico: rochchristianjohnson@gmail.com
Copia de seguridad de contactos de estudio
- Nombre: Esai ANAGONOU, PhD
- Número de teléfono: +229(01)96826567
- Correo electrónico: esaianagonou@yahoo.fr
Ubicaciones de estudio
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Pobé
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Pobé, Pobé, Benín
- Centre de Dépistage et de Traitement de la Lèpre et de l'Ulcère de Buruli (Raoul et Madeline Follereau) de Pobè
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Contacto:
- Esai ANAGONOU, PhD
- Número de teléfono: +229(01)96826567
- Correo electrónico: esaianagonou@yahoo.fr
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Contacto:
- Oswald ATTOLOU, Master
- Número de teléfono: +229(01)94401778
- Correo electrónico: oattolou@raoul-follereau.org
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Investigador principal:
- Akimath Olagnidé Pélagie HABIB, Master
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-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Be an individual aged 18-60 years.
- Has been diagnosed with MB leprosy with a Bacillary Index (BI) of at least 2+ on a slit skin smear (SSS).
- Have no prior leprosy treatment (WHO MDT and/or dapsone monotherapy).
- Be able to give voluntary informed consent.
- Be able to complete the full study period and follow-up (with no planned migration and an accurate, known and accessible address).
- Be able to accept hospitalisation for at least three months (site-specific requirement).
- "Body weight < 85 kg at screening." (participants with weight >= 85 kg have an increased risk of severe transaminitis under telacebec)
Exclusion Criteria:
- Unable to give voluntary informed consent.
- Is a pregnant or breastfeeding woman.
- Presenting with reinfection or relapse after WHO MDT/dapsone monotherapy, or has received anti-mycobacterial drugs in the last 30 days.
- Presenting a leprosy reaction at diagnosis.
- Being currently involved or having been involved within the last 30 days in a clinical trial.
- Has any of the following medical conditions: a baseline QTcF of >450 ms or a clinically significant ECG abnormality or significant heart disease; HIV co-infection; HBV co-infection; history of or current pancreatitis; known or suspected cirrhosis of the liver; active clinical tuberculosis; any condition which, in the opinion of the investigator, may cause harm to the patient; known alcohol or drug addiction; known uncontrolled chronic disease such as diabetes (HbA1c >10%) or renal failure (GFR <50 ml/min); anaemia requiring transfusion.
- Known glucose-6-phosphate dehydrogenase (G6PD) deficiency, due to risk of dapsone-induced haemolytic anaemia (G6PD testing required at screening).
- Abnormal screening laboratory values, including: WBC <2.5 × 10⁹/L; Neutrophils <1.0 × 10⁹/L; Platelets <100 × 10⁹/L; AST or ALT >2 times the upper limit of the reference range; Albumin <30 mg/dL; Bilirubin >2 mg/dL (34 μmol/L); Calculated creatinine clearance (Cockcroft-Gault) <50 ml/min; Lipase ≥1.6 times the upper limit of the reference range.
Other eligibility consideration - Contraception
All women of reproductive potential must be tested for pregnancy at screening, and again before dosing at baseline (Day 0) and on Days 28, 42, 56, and 84 of the experimental treatment phase. Women with a positive pregnancy test after enrolment will have their treatment shifted to MDT if randomised to a telacebec-containing arm.
All women of reproductive potential must use two reliable and effective methods of contraception simultaneously while taking the study medication and up to two months after the last dose of telacebec. One highly effective form of contraception must be used (hormonal, IUD, prior tubal ligation, or partner's prior vasectomy) plus one additional effective method (male latex or synthetic condom, diaphragm or cervical cap). Male participants whose female partners are of reproductive age must also use contraception for up to 90 days after the last telacebec dose.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Sin intervención: (Group A) receiving standard WHO multidrug therapy (MDT)
The World Health Organization recommends Multidrug Therapy (MDT) to cure leprosy. This standard treatment combines three medicines: (Rifampicin 300mg x 2) + (Clofazimin 100 mg x 3) + (Dapsone 50 mg) x 12 months |
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|
Experimental: Group B (Low dose)
(Telacebec 100 mg x 3 once monthly x 3 months) followed by (Rifampicin 300mg x 2) + (Clofazimin 100 mg x 3) + (Dapsone 50 mg) x 12 months |
Telacebec 300 mg once monthly × 3 months |
|
Experimental: Group C (Hight dose)
(Telacebec 100 mg x 6 once monthly x 3 months) followed by (Rifampicin 300mg x 2) + (Clofazimin 100 mg x 3) + (Dapsone 50 mg) x 12 months |
Telacebec 600 mg once monthly × 3 months |
|
Experimental: Group D (Combinaison)
(Telacebec 100 mg x 3 + Rifampicin 300 mg x 2 once monthly x 3 months) followed by (Rifampicin 300mg x 2) + (Clofazimin 100 mg x 3) + (Dapsone 50 mg) x 12 months |
(Telacebec 300 mg + Rifampicine 600 mg) once monthly x 3 months |
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change from baseline in viable Mycobacterium leprae load in participants' skin lesions
Periodo de tiempo: Baseline (Day 0) and Day 84
|
Treatment response of leprosy infection in each participant, measured in skin biopsies taken from the same lesion at baseline and Day 84 using the Molecular Viability Assay (MVA): quantitative RT-PCR of esxA and hsp18 transcripts, standardised to 3,000 bacilli. Reported as change in log10 viability; a larger decrease indicates a greater bactericidal effect of treatment in the participant. Arms B, C and D are compared with standard WHO MB-MDT (Arm A) |
Baseline (Day 0) and Day 84
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of participants with treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
Periodo de tiempo: From first dose through Day 84 (end of study drug period)
|
Clinical and laboratory adverse events, graded for severity and assessed for relationship to study drug, in participants receiving telacebec 300 mg, telacebec 600 mg, telacebec 300 mg + rifampicin 600 mg, or WHO MB-MDT |
From first dose through Day 84 (end of study drug period)
|
|
Proportion of participants with clinical improvement of leprosy skin lesions
Periodo de tiempo: Day 84 and Month 12 (end of treatment)
|
Assessed with standardised lesion-response criteria based on clinical examination and standardised photographs, classified as clear, moderate or no improvement. Classification validated by an independent external expert panel. |
Day 84 and Month 12 (end of treatment)
|
|
Incidence and severity of leprosy reactions
Periodo de tiempo: Baseline through Month 24 (end of follow-up)
|
Number of participants with Type 1 (reversal) reactions, defined by WHO criteria, and Type 2 reactions (erythema nodosum leprosum). ENL severity scored with the ENLIST ENL Severity Scale (EESS). |
Baseline through Month 24 (end of follow-up)
|
|
Change in peripheral nerve sensory function
Periodo de tiempo: Baseline, Day 84, Month 12, Month 24
|
Semmes-Weinstein monofilament thresholds at standardised sites of the hands and feet. |
Baseline, Day 84, Month 12, Month 24
|
|
Change in peripheral nerve motor function
Periodo de tiempo: Baseline, Day 84, Month 12, Month 24
|
Voluntary Muscle Testing (VMT) scores. |
Baseline, Day 84, Month 12, Month 24
|
|
Number of participants with new nerve function impairment
Periodo de tiempo: Baseline through Month 24
|
Baseline through Month 24
|
|
|
Change in health-related quality of life (EQ-5D)
Periodo de tiempo: Baseline, Day 84, Month 12
|
Baseline, Day 84, Month 12
|
Otras medidas de resultado
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Participant-reported global impression of change (PGI-C)
Periodo de tiempo: Day 84, Month 12
|
Day 84, Month 12
|
|
|
Proportion of participants with viable M. leprae in skin lesions
Periodo de tiempo: Baseline and Day 84
|
Skin biopsy material from a subset of participants (5 to 6 per group) are tested: Data reported per participant (presence of viable bacilli on day 84 compared to that participant's baseline sample). |
Baseline and Day 84
|
|
Change from baseline in M. leprae rRNA synthesis (RS) ratio in participants' skin lesions
Periodo de tiempo: Baseline and Day 84
|
Marker of ongoing bacterial replication in each participant's lesion |
Baseline and Day 84
|
|
Number of participants who discontinue or interrupt study treatment because of adverse events
Periodo de tiempo: Throught Day 84
|
Throught Day 84
|
|
|
Number of participants with treatment-emergent laboratory abnormalities
Periodo de tiempo: Throught Day 84
|
Haematology, biochemistry and liver function tests |
Throught Day 84
|
|
Plasma concentration of telacebec in participants
Periodo de tiempo: Day 0 through Day 84
|
Sparse pharmacokinetic sampling |
Day 0 through Day 84
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Investigadores
Investigadores
- Investigador principal: Roch Christian JOHNSON, Medical Doctor, PhD, HDR, Centre Interfacultaire de Formation et de Recherche en Environnement pour le Développement Durable (CIFRED), University of Abomey-Calavi
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Infecciones
- Infecciones por bacterias grampositivas
- Infecciones bacterianas
- Infecciones bacterianas y micosis
- Infecciones por Actinomycetales
- Infecciones por micobacterias
- Infecciones por Mycobacterium, no tuberculosas
- Lepra
- Lepra Multibacilar
- Compuestos heterocíclicos
- Compuestos heterocíclicos, anillo fusionado
- Compuestos policíclicos
- Compuestos heterocíclicos, 4 o más anillos
- Rifamycinas
- Lactamas, macrocíclicas
- Compuestos macrocíclicos
- Rifampicina
- telacebec
Otros números de identificación del estudio
Otros números de identificación del estudio
- TEB-LEP2025-01
- 101190742 (Otro número de subvención/financiamiento: European Union)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
The plan is not yet developed
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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