NCT05972954已完成2 期
A Phase 2a Safety, Tolerability, and Pharmacodynamic Study of OMT-28 in PMD Patients With Myopathy and/or Cardiomyopathy and Inflammation (PMD-OPTION)
适应症
干预措施
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 28
- 试验地点
- 9
- 主要终点
- Responder rate
研究概览
简要总结
The goal of this clinical trial is to learn about the treatment effects of the investigational new drug OMT-28 in patients with Primary Mitochondrial Disease.
The main question[s] it aims to answer are:
- Is OMT-28 safe and well tolerated in this patient population?
- Does OMT-28 reduce Growth Differentiation Factor 15 (GDF-15) and other relevant blood markers of mitochondrial dysfunction and inflammation?
- Does OMT-28 improve symptoms of the disease, e.g. fatigue or exercise intolerance?
Participants will be asked to participate in 6 study visits at an experienced clinical center, including physical examinations and exercise tests, and take the study medication regularly once per day according to the protocol.
Researchers will compare for every participant the results after 3 months and 6 months of treatment with a preceding 3 month period of standard care treatment to investigate the effects of OMT-28 on clinical parameters and a number of blood parameters.
详细描述
This is an open label, single-arm, multiple-phase and multicenter Phase 2a study to evaluate the efficacy, safety, and pharmacokinetics of a single OMT-28 dose (24 mg given once daily) in patients with Primary Mitochondrial Disease and clinical manifestation of myopathy and/or cardiomyopathy.
Patients are eligible if they have
- Primary Mitochondrial Disease with a documented mitochondrial transfer ribonucleic acid (tRNA) point mutation, including m3243A>G, m8344A>G, or single mitochondrial DNA (mtDNA) deletions,
- a clinically relevant myopathy and/or cardiomyopathy confirmed following standard guidelines,
- a blood plasma GDF-15 concentration > 1200 ng/L and < 10.000 ng/L at screening
Participation in the study is divided into 3 parts:
- Screening and baseline: 12 weeks
- Treatment: 24 weeks
- Safety follow-up: 4 weeks
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Documented mutation resulting in mitochondrial disease: mitochondrial tRNA point mutations, including m3243A>G, m8344A>G, and single mtDNA deletions
- •Diagnosis of Cardiomyopathy defined as LV hypertrophy and/or LVEF<50% and/or late gadolinium enhancement on cardiac MRI and/or Myopathy as defined by the International Workshop: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adult (Mancuso et al. 2017[8])
- •GDF-15 between 1,200 ng/L and 10,000 ng/L at screening
- •Ability to perform the exercise tests
- •6. Willing and able to provide a signed Informed Consent, as well as written documentation in accordance with country and local privacy requirements, e.g., written data protection consent
- •Able and willing to comply with the requirements of this study protocol
- •Both female patients, as well as, female partners of male patients who are of child-bearing potential must be willing to not become pregnant for the complete duration of the study (30 days after the last dose of study medication).
排除标准
- •Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study
- •Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data
- •Subjects with a history of cancer in the last 5 years
- •Hypertension defined as systolic BP >160 mmHg or diastolic BP >100 mmHg at screening
- •Uncontrolled Diabetes mellitus according to investigator's assessment
- •Stroke-like episodes or seizures occurred within last 6 months
- •Motoric abnormalities other than related to the mitochondrial disease interfering with the outcome parameters
- •History or evidence of active tuberculosis (TB) infection, any co-disease with inflammatory condition (e.g., Inflammatory Bowel Disease (IBD) etc.)
- •Patients with a positive hepatitis panel and/or positive immunodeficiency virus test at screening
- •Regular use of steroid, non-steroidal anti-inflammatory drug (NSAID), or colchicine within 30 days before screening
- •Chronic use of Metformin
- •Use of fish oil / omega-3 fatty acid supplements within two weeks before screening
- •Drinking more than 9 standard cups of alcohol per week and/or more than 3 standard cups of alcohol per occasion
- •Positive drug and alcohol screen (including opiates, methadone, cocaine, amphetamines [including ecstasy], cannabinoids, barbiturates, benzodiazepines)
- •Any significant hepatic disease
- •Receiving any investigational therapy or any approved therapy for investigational use within 30 days or 5 half-lives prior to screening (whichever is longer)
- •Received any vaccines (including the booster vaccination for COVID-19) within two weeks prior to Visit 1
- •Females of childbearing potential (those who are not surgically sterilized or post-menopausal for at least 1 year) are excluded from participation in the study unless they agree to use adequate contraception as described in Appendix 11.4
- •Males (including sterilized subjects) and whose female partners have child-bearing potential, must agree to use male contraception (condoms) during the period from the time of signing the informed consent form (ICF) through 30 days after the last dose of study drug. They must agree to immediately inform the investigator if his partner becomes pregnant during the study
- •Subjects who have previously been exposed to OMT-28, whether responder or non-responder.
- •Any use of statins (HMG-CoA reductase inhibitors)
- •Use of quinine, tacrolimus, mycophenolate mofetil, ciclosporin, serotine receptor-type 1 agonist, penicillin G, penicillamine (d-penicillamine), nicotinic acid (niacin), colchicine, isotretinoin, and amiodarone, peroxisome proliferator-activated receptor (PPAR) activators, AMP-activated protein kinase (AMPK) activators, sirtuin activators, steroids, cyclooxygenase inhibitors.
研究组 & 干预措施
Treatment with OMT-28
Experimental
24mg OMT-28, oral capsule, for 12 weeks
干预措施: OMT-28 (Drug)
结局指标
主要结局
Responder rate
时间窗: 12 weeks treatment vs. 12 weeks baseline
Number of patients (responder rate) with a between phase difference in GDF-15 of at least 20% decrease
Number of Treatment Emergent Adverse Events (TEAE)
时间窗: up to 28 weeks
Compare the number of TEAEs during and between evaluation phases
次要结局
- Pharmacokinetics: Cmax [ng/ml](week 12 and week 24)
- Responder rate(24 weeks treatment vs. 12 weeks baseline)
- Change in plasma concentration of GDF-15 [ng/L](12 weeks treatment vs. 12 weeks baseline)
- Pharmacokinetics: Ctrough [ng/ml](weeks 12, 16, 24 and 28)
研究者
研究点 (9)
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