Accelerating the Development of Pan-TB Regimens

Successfully treating TB can be complex and challenging. New regimens with little to no drug resistance – known as pan-TB regimens – create a simpler and more effective treatment pathway for all people diagnosed with TB.

The Project to Accelerate New Treatments for Tuberculosis (PAN-TB) is a first-of-its-kind collaboration among philanthropic, non-profit and private-sector organizations that aims to accelerate the identification of promising pan-TB regimens and conduct research through phase 2b/2c clinical trials. These pan-TB regimens will be designed to have improved safety and tolerability, a shorter duration, and simpler to use than existing treatment options.

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New clinical study data now accessible via the Critical Path Institute

Data from the PAN-TB Collaboration’s first clinical trial are now available through the Critical Path Institute Data Analytics Platform (CP-DAP). The PAN-TB Collaboration is pleased to offer access to this data in the continued spirit of open information sharing to support the broader TB Drug Development ecosystem. 

The trial was discontinued in 2025 after data showed that neither regimen was potent enough to achieve the study’s goal of shortening treatment to three months. While the regimens did not meet that goal, the findings are informing the development of future PAN-TB regimens, and making the data available will allow researchers across the field to continue learning from the study. 

This study evaluated five antimicrobial agents across two combination regimens for treating drug-susceptible tuberculosis (TB) with shorter treatment durations (reducing treatment time from the current six months duration to four months or less). 

The two investigational drug regimen combinations evaluated were: 

  • DBQS – delamanid, bedaquiline, quabodepistat and sutezolid 
  • PBQS – pretomanid, bedaquiline, quabodepistat and sutezolid

All available data are mapped to the Clinical Data Interchange Standards Consortium (CDISC) Standard for Exchange of Nonclinical Data (SEND). Please note that C-Path has migrated to an enhanced platform, which will provide expanded functionality and capabilities for researchers. All available PAN-TB Collaboration clinical and nonclinical data can be requested through the new platform.  

To request access to these data, please visit and create a user login via the CP-DAP landing page; helpful, step-by-step tutorials may be accessed from the top right-hand corner. For any additional questions, please reach out to [email protected]. The clinical data may be found in CP-DAP’s Tuberculosis collection as “Project to Accelerate New Treatments for Tuberculosis: Clinical [SDTM] 

Request Access

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Overview of Partners

The members of the PAN-TB Collaboration have committed to leveraging their unique assets, resources and scientific expertise to advance the development of novel regimens.

PAN-TB Priority Candidates

  • Bedaquiline
    Registered product for multidrug-resistant TB, Johnson & Johnson, New Chemical Entity for drug-sensitive TB, TB Alliance
    Bedaquiline
  • Delamanid
    Registered product, Otsuka Pharmaceutical Co., Ltd
    Delaminid
  • Pretomanid
    Registered product, TB Alliance
    Pretamonid
  • Sutezolid
    New Chemical Entity, TB Alliance Medicine Patent Pool, Gates Medical Research Institute
    Sutezolid
  • GSK-286
    New Chemical Entity, GSK
    GSK-286
  • GSK-830
    New Chemical Entity, GSK
  • Quabodepistat
    New Chemical Entity, Otsuka Pharmaceutical Co., Ltd
    quabodepistat
  • Sorfequiline
    New Chemical Entity, TB Alliance
    TBAJ-876
  • TBD09
    New Chemical Entity, Gates Medical Research Institute, Merck
  • TBD11
    New Chemical Entity, Gates Medical Research Institute, Calibr