Boji Medical Technology Receives NMPA Approval for TBA Clinical Study in Drug-Resistant Tuberculosis

Boji Medical Technology Receives NMPA Approval for TBA Clinical Study in Drug-Resistant Tuberculosis

China-based Clinical Research Organization (CRO) Boji Medical Technology Co., Ltd. (SHE: 300404) has announced receiving approval from the National Medical Products Administration (NMPA) to conduct a clinical study for TBA, a novel treatment for drug-resistant pulmonary tuberculosis.

TBA: A New Approach to Combating Drug-Resistant Tuberculosis
The Category 1 chemical drug, co-developed by Guangdong Gumadi Health Technology Co., Ltd, features a distinct new structure and pharmacological effects that set it apart in the fight against tuberculosis. TBA’s mechanism of action involves targeting QcrB in the electron transport chain of Mycobacterium, thereby inhibiting the bacteria’s respiratory function and offering a new avenue for treatment.

Potential Impact of TBA on Tuberculosis Treatment
The approval to proceed with clinical studies for TBA marks a significant step forward in the development of innovative treatments for drug-resistant pulmonary tuberculosis. This disease remains a significant global health challenge, and the introduction of new drugs with unique mechanisms of action could potentially transform patient outcomes and improve treatment success rates.-Fineline Info & Tech

Insight, China's Pharmaceutical Industry