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Study on the Effectiveness and Safety of Carrimycin in the Treatment of Mycobacterium Abscessive Pulmonary Disease

Study on the Effectiveness and Safety of Carrimycin in the Treatment of Mycobacterium Abscessive Pulmonary Disease

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054540
Enrollment
Unknown
Registered
2021-12-19
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mycobacterium Abscessive Pulmonary Disease

Interventions

Experimental group:MAB-PD treatment including carrimycin

Sponsors

Shanghai Pulmonary Hospital Affiliated to Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The subject or legal representative has signed the informed consent; 2. Aged 18 to 75 years; 3. Diagnosed as non-tuberculous mycobacterial lung disease in accordance with the "Nontuberculous Mycobacteria Diagnosis Group Standard T/CHATA001-2020"; 4. The etiology of sputum or lavage fluid culture is clearly Mycobacterium abscessus; 5. Have not received non-tuberculous mycobacteria treatment in the past; 6. Culture drug susceptibility to rule out macrolide resistance.

Exclusion criteria

Exclusion criteria: 1. Clearly combined infection with other pathogenic microorganisms, including fungi, viruses, mycoplasma, and Mycobacterium tuberculosis; 2. Participated in any clinical trial within the past 1 month; 3. Combined with primary diseases that seriously affect survival expectations: transplantation status, uremia, malignant tumor; 4. Take immune-related drugs within the past 1 month, such as spleen aminopeptide, thymosin, etc.; 5. Pregnant women, lactating women, subjects (including male subjects) who have a pregnancy plan (including sperm donation and egg donation plan) in the next 6 months or are unable to take effective contraceptive measures; 6. Patients deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Chest imaging;Early bactericidal activity;Sputum bacteria turn negative rate;

Countries

China

Contacts

Public ContactSha Wei

Shanghai Pulmonary Hospital Affiliated to Tongji University

13671758200@126.com+86 13671758200

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026