An Open-label, Non-controlled, Multicentre, Pilot Clinical Trial of Inhaled Molgramostim in Subjects With Antibiotic-resistant Non-tuberculosis Mycobacterial (NTM) Infection
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- Savara Inc.
- 入组人数
- 32
- 试验地点
- 5
- 主要终点
- Number of Participants With Sputum Culture Conversion to Negative
研究概览
简要总结
The trial is an open-label, non-controlled, multicenter, pilot clinical trial of inhaled molgramostim (recombinant human granulocyte-macrophage colony stimulating factor; rhGM-CSF) in subjects with persistent pulmonary non-tuberculous mycobacterial (NTM) infection. Participants will be treated for 24-weeks with inhaled molgramostim and followed up for 12-weeks after end of treatment. The primary aim of the trial is to investigate the efficacy of inhaled molgramostim on NTM sputum culture conversion to negative.
详细描述
The study will comprise a Screening Visit, a Baseline Visit, a 24-week treatment period and a 12-week follow-up period. 30 adult participants with a history of chronic NTM infection with at least 2 positive cultures in the prior 2 years, of which at least one is within the last 6 months prior to Screening, will be considered for enrollment. Participants should provide a positive NTM sputum culture at Screening to be eligible.
Two subgroups of participants will be recruited:
- Group 1: Participants who remain sputum culture positive while currently on a multidrug NTM guideline based antimycobacterial regimen, which has been ongoing for at least 6 months prior to the Baseline Visit.
- Group 2: Participants who remain sputum culture positive but have either stopped a multidrug NTM guideline based antimycobacterial regimen at least 28 days prior to Screening due to lack of response or intolerance, or never started such treatment.
The treatment period will consist of 14 trial visits (Screening [within 10 weeks of Baseline], Baseline, and every 4 weeks to Week 48 [visits at Weeks 28, 36 and 44 included telephone contact, others included clinic visits]) and a Follow-up visit 12 weeks after the end of treatment.
At the Baseline visit, eligible participants will start treatment with molgramostim nebulizer solution, 300 μg, administered by inhalation using an eFlow Nebulizer System. At each visit, sputum samples will be collected for staining and microscopy, and microbiological culture. In addition, clinical assessments including body weight, patient reported outcomes, and diffusion capacity of the lung for carbon monoxide (DLCO) will be conducted at each clinic visit. Spirometry will be assessed at Baseline, and at Weeks 12, 24, 32, 40 and 48. A 6-minute walk test (6-MWT) will be conducted at Baseline, at Weeks 12, 24, 48 and at the 12-week Follow-up visit. Safety laboratory samples will be collected at Screening, Baseline and at Weeks 4, 12, 24, 32, 40, 48 and at the 12-week Follow-up visit. Anti-GM-CSF antibodies will be assessed at Baseline, at Week 4, 12, 24, 32, 48, and at the 12-week Follow-up visit.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •History of chronic pulmonary infection with MAC or M. abscessus (defined as at least 2 documented positive sputum cultures in the prior 2 years, of which at least one was obtained in the 6 months prior to Screening).
- •Subject fulfills one of the following criteria:
- •Subjects who remain sputum culture positive while currently on a multidrug NTM guideline based antimycobacterial regimen, which has been ongoing for at least 6 months prior to the Baseline Visit
- •Subjects who remain sputum culture positive but have either stopped a multidrug NTM guideline based antimycobacterial regimen at least 28 days prior to Screening due to lack of response or intolerance, or never started such treatment.
- •Ability to produce at least 2 mL of sputum or be willing to undergo an induction that produces at least 2 mL of sputum for clinical evaluation.
- •Female or male ≥18 years of age.
- •Females who have been post-menopausal for more than 1 year or females of childbearing potential after a confirmed menstrual period using a highly efficient method of contraception (i.e. a method with less than 1% failure rate such as combined hormonal contraception, progesterone-only hormonal contraception, intrauterine device, intrauterine hormone- releasing system, bilateral tubal occlusion, vasectomized partner, sexual abstinence), during and until thirty (30) days after last dose of trial treatment. Females of childbearing potential must have a negative serum pregnancy test at Screening (Visit 1) and a negative urine pregnancy test at dosing at Baseline (Visit 2) and must not be lactating.
- •Males agreeing to use condoms during and until thirty (30) days after last dose of medication, or males having a female partner who is using adequate contraception as described above.
- •Willing and able to provide signed informed consent.
- •Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other trial procedures specified in the protocol as judged by the investigator
排除标准
- •Subjects diagnosed with cystic fibrosis.
- •Prior therapy with inhaled or systemic GM-CSF.
- •Subjects with hemoptysis of ≥60 mL in a 24 hour period within 4 weeks prior to Screening.
- •Concurrent disease with a life expectancy of less than 6 months.
- •History of, or present, myeloproliferative disease, leukemia or other hematological malignancy.
- •Active pulmonary malignancy (primary or metastatic); or any malignancy requiring chemotherapy or radiation therapy within one year prior to Screening or anticipated during the study period.
- •Active allergic bronchopulmonary mycosis or connective tissue disease, inflammatory bowel disease or other autoimmune disorder requiring therapy associated with significant immunosuppression, such as systemic corticosteroids at a dose equivalent of 10 mg/day or more of prednisolone, within 3 months prior to Screening or anticipated during the study period.
- •Pulmonary tuberculosis requiring treatment or treated within 2 years prior to Screening.
- •HIV infection or other disease associated with significant immunodeficiency.
- •History of lung transplantation.
- •Any change in chronic NTM multi-drug antimycobacterial regimen within 28 days prior to Screening.
- •Treatment with any investigational medicinal product within 3 months of Screening.
- •Previous experience of severe and unexplained side-effects during aerosol delivery of any kind of medicinal product
- •Any other serious medical condition which in the opinion of the investigator would make the subject unsuitable for the trial.
研究组 & 干预措施
Inhaled molgramostim/antimycobacterials
Inhaled molgramostim administered in participants who remain sputum culture positive while currently on a multidrug NTM guideline-based antimycobacterial regimen, which has been ongoing for at least 6 months prior to the Baseline Visit
干预措施: Inhaled molgramostim (Drug)
Inhaled molgramostim/antimycobacterials
Inhaled molgramostim administered in participants who remain sputum culture positive while currently on a multidrug NTM guideline-based antimycobacterial regimen, which has been ongoing for at least 6 months prior to the Baseline Visit
干预措施: Antimycobacterial regimen (Drug)
Inhaled molgramostim
Inhaled molgramostim administered in participants who remain sputum culture positive but have stopped a multidrug NTM guideline-based antimycobacterial regimen at least 28 days prior to Screening due to lack of response or intolerance, or who never started such treatment
干预措施: Inhaled molgramostim (Drug)
结局指标
主要结局
Number of Participants With Sputum Culture Conversion to Negative
时间窗: 48 weeks
Sputum culture conversion is defined as at least 3 consecutive sputum samples without growth of NTM during the treatment period.
次要结局
- Change From Baseline in Symptom Scores (Assessed Using Quality of Life Questionnaire - Bronchiectasis (QOL-B))(Baseline to Week 48)
- Change From Baseline in Global Rating of Health (GRH)(Baseline to Week 48)
- Change From Baseline in Diffusing Capacity of the Lung for Carbon Monoxide (DLCO)(Baseline to Week 48)
- Number of Participants With Durable Sputum Smear Conversion(60 weeks)
- Number of Serious AEs (SAEs) During the Trial Period(60 weeks)
- Number of Adverse Drug Reactions (ADRs) During the Trial Period(60 weeks)
- Number of Severe AEs During the Trial Period(60 weeks)
- Number of Participants With Sputum Smear Conversion to Negative(48 weeks)
- Number of Participants With Durable Sputum Culture Conversion(60 weeks)
- Change From Baseline in Symptom Scores (Assessed Using Lower Respiratory Tract Infections - Visual Analogue Scale)(Baseline to Week 48)
- Number of Participants Withdrawn From Treatment Due to an AE During the Trial Period(60 weeks)
- Number of Subjects With Development of Anti-GM-CSF Antibodies in Serum(60 weeks)
- Change From Baseline in Body Weight(Baseline to Week 48)
- Change From Baseline in 6-Minute Walking Distance (6MWD)(Baseline to Week 48)
- Change From Baseline in Dyspnea Scores During a 6MWT(Baseline to Week 48)
- Number of Adverse Events (AEs) During the Trial Period(60 weeks)
- Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1) (% Predicted)(Baseline to Week 48)
- Change From Baseline in Forced Vital Capacity (FVC) (% Predicted)(Baseline to Week 48)