Clinical Study on the Early Bactericidal Activity of Contezolid Against Mycobacterium Abscessus D… (NCT07372781) | Clinical Trial Compass
By InvitationPhase 2
Clinical Study on the Early Bactericidal Activity of Contezolid Against Mycobacterium Abscessus Disease
China24 participantsStarted 2026-01-01
Plain-language summary
This study is a single-center, randomized, controlled, open-label clinical trial designed to assess the early bactericidal activity of a single agent, contezolid, in patients with Mycobacterium abscessus infections. Patients were administered contezolid monotherapy for 14 days specifically targeting Mycobacterium abscessus, and were compared to a control group receiving linezolid, a classic anti-Mycobacterium abscessus drug. The comparison was conducted through the analysis of colony forming units counts and Time To Positivity in sputum cultures. By evaluating the impact of contezolid monotherapy on the bacterial load in the sputum of patients with Mycobacterium abscessus infections, this study aimed to assess the early bactericidal activity of contezolid, thereby providing a basis for the selection of new therapeutic options for the treatment of patients with Mycobacterium abscessus infections.
Who can participate
Age range18 Years – 65 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Male or female aged between 18 and 65 years old;
* Weight ranging from 40 kg to 90 kg;
* At least one positive sputum culture for Mycobacterium abscessus within 6 months prior to screening, and one positive sputum culture for Mycobacterium abscessus with molecular species identification during the screening period within 1 month prior to the study;
* Voluntary participation in this study and signing of the informed consent form; (5) Male and female participants must use effective contraception during the study and for 1 month after the study ends.
Exclusion Criteria:
* Patients who have been on long-term corticosteroid therapy or taking immunosuppressants within 90 days prior to screening;
* Pregnant women, postpartum women, and lactating patients;
* Patients with a history of bedaquiline allergy or known hypersensitivity, or a history of severe adverse reactions;
* Patients with evidence of bedaquiline resistance;
* Patients deemed unsuitable for participation in this study by the investigator's assessment;
* Patients whom the investigator believes participation in this study would harm their health, or who are unlikely to comply with the scheduled visits and assessments as outlined in the protocol, and therefore are not suitable for participation in this study.