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.
研究概览
详细说明
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.
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Roch Christian JOHNSON, Medical Doctor, Phd, HDR
- 电话号码:+229(01)96221132
- 邮箱:rochchristianjohnson@gmail.com
研究联系人备份
- 姓名:Esai ANAGONOU, PhD
- 电话号码:+229(01)96826567
- 邮箱:esaianagonou@yahoo.fr
学习地点
-
-
Pobé
-
Pobé、Pobé、贝宁
- Centre de Dépistage et de Traitement de la Lèpre et de l'Ulcère de Buruli (Raoul et Madeline Follereau) de Pobè
-
接触:
- Esai ANAGONOU, PhD
- 电话号码:+229(01)96826567
- 邮箱:esaianagonou@yahoo.fr
-
接触:
- Oswald ATTOLOU, Master
- 电话号码:+229(01)94401778
- 邮箱:oattolou@raoul-follereau.org
-
首席研究员:
- Akimath Olagnidé Pélagie HABIB, Master
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
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.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
无干预:(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 |
|
|
实验性的: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 |
|
实验性的: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 |
|
实验性的: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 |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change from baseline in viable Mycobacterium leprae load in participants' skin lesions
大体时间: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
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of participants with treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间:Baseline through Month 24
|
Baseline through Month 24
|
|
|
Change in health-related quality of life (EQ-5D)
大体时间:Baseline, Day 84, Month 12
|
Baseline, Day 84, Month 12
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Participant-reported global impression of change (PGI-C)
大体时间:Day 84, Month 12
|
Day 84, Month 12
|
|
|
Proportion of participants with viable M. leprae in skin lesions
大体时间: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
大体时间: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
大体时间:Throught Day 84
|
Throught Day 84
|
|
|
Number of participants with treatment-emergent laboratory abnormalities
大体时间:Throught Day 84
|
Haematology, biochemistry and liver function tests |
Throught Day 84
|
|
Plasma concentration of telacebec in participants
大体时间:Day 0 through Day 84
|
Sparse pharmacokinetic sampling |
Day 0 through Day 84
|
合作者和调查者
合作者
调查人员
- 首席研究员: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
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- TEB-LEP2025-01
- 101190742 (其他赠款/资助编号:European Union)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
The plan is not yet developed
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研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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