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Telacebec in Adults With Multibacillary Leprosy (TEBULA Leprosy Trial) (TEBULA LEPROSY)

30 de outubro de 2026 atualizado por: Fondation Raoul Follereau

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.

Visão geral do estudo

Descrição detalhada

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 estudo

Intervencional

Inscrição (Estimado)

120

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Pobé
      • Pobé, Pobé, Benim
        • Centre de Dépistage et de Traitement de la Lèpre et de l'Ulcère de Buruli (Raoul et Madeline Follereau) de Pobè
        • Contato:
        • Contato:
        • Investigador principal:
          • Akimath Olagnidé Pélagie HABIB, Master

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 60 anos (Adulto)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: (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

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

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in viable Mycobacterium leprae load in participants' skin lesions
Prazo: 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 resultados secundários

Medida de resultado
Descrição da medida
Prazo
Number of participants with treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: Baseline through Month 24
Baseline through Month 24
Change in health-related quality of life (EQ-5D)
Prazo: Baseline, Day 84, Month 12
Baseline, Day 84, Month 12

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Participant-reported global impression of change (PGI-C)
Prazo: Day 84, Month 12
Day 84, Month 12
Proportion of participants with viable M. leprae in skin lesions
Prazo: 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
Prazo: 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
Prazo: Throught Day 84
Throught Day 84
Number of participants with treatment-emergent laboratory abnormalities
Prazo: Throught Day 84

Haematology, biochemistry and liver function tests

Throught Day 84
Plasma concentration of telacebec in participants
Prazo: Day 0 through Day 84

Sparse pharmacokinetic sampling

Day 0 through Day 84

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de dezembro de 2026

Conclusão Primária (Estimado)

1 de novembro de 2028

Conclusão do estudo (Estimado)

1 de novembro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

21 de setembro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

30 de outubro de 2026

Primeira postagem (Real)

5 de novembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

5 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

30 de outubro de 2026

Última verificação

1 de outubro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

The plan is not yet developed

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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