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临床试验/NCT07228702
NCT07228702Enrolling By Invitation1 期

Bacteriophage Therapy for Mycobacterium Abscessus Pulmonary Infection: An Open Label Individual Patient Study

Vancouver Coastal Health2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2026年1月11日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
Enrolling By Invitation
入组人数
1
试验地点
2
主要终点
Microbiologic: Response

研究概览

简要总结

This study aims to use mycobacteriophage therapy, using identified in-vitro effective Mycobacteriophage Muddy_HRMN0052, along with combination conventional antimycobacterial therapy for their NTM pulmonary disease with Mycobacterium abscessus with goal to reduce infection burden and improve pulmonary disease

详细描述

Hypothesis

Hypothesis: Mycobacteriophage therapy, using identified in-vitro effective Mycobacteriophage Muddy_HRMN0052, along with combination conventional antimycobacterial therapy for their NTM pulmonary disease with MABS will reduce infection burden and improve pulmonary disease.

Objectives:

  1. Efficacy - Assess MABS pulmonary disease response mycobacteriophage therapy
  2. Safety - Determine tolerability and off target effects of IV and inhaled mycobacteriophage therapy

Specific End Points (during and post treatment up to last clinical follow-up (>24month):

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

性别
Female
接受健康志愿者

入选标准

  • This is an individual patient expanded access study specific to one individual based on tailor intervention (Mycobacteriophage)
  • Inclusion Criteria:
  • consent to participation

排除标准

  • non-consent to participation

研究组 & 干预措施

Treatment

Experimental

Use of mycobacteriophage

干预措施: Mycobacteriophage Muddy_HRMN0052 (Biological)

Treatment

Experimental

Use of mycobacteriophage

干预措施: Amikacin Injection (Drug)

Treatment

Experimental

Use of mycobacteriophage

干预措施: Clofazimine (Drug)

Treatment

Experimental

Use of mycobacteriophage

干预措施: Bedaquiline (B) (Drug)

Treatment

Experimental

Use of mycobacteriophage

干预措施: Linezolid (LZD) (Drug)

Treatment

Experimental

Use of mycobacteriophage

干预措施: Sulfamethoxazole/Trimethoprim (Drug)

结局指标

主要结局

Microbiologic: Response

时间窗: 2 years

1\. Sputum culture status: time (days) to durable sputum culture conversion (no mycobacterial growth on 3 sputum sample)

次要结局

  • Microbiologic: Resistance development(2 years)
  • Clinical: Symptoms(2 year)
  • Clinical: Sputum(2 year)
  • Clinical: Radiographic(2 year)
  • Clinical: Pulmonary Function(2 year)
  • Clinical: Symptoms(2 year)
  • Clinical: Sputum(2 year)
  • Microbiologic: Resistance development(2 years)
  • Clinical: Radiographic(2 year)
  • Clinical: Pulmonary Function(2 year)
  • Microbiologic: Neutralizing antibody status.(2 years)
  • Clinical: Adverse effects(2 year)

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

William Connors

Clinical Associate Professor

Vancouver Coastal Health

研究点 (2)

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