1 / 14

Karel de Beule, CDTL TMC 207

Interim analysis of a double-blind, placebo-controlled study with TMC207 in patients with Multi-Drug Resistant (MDR) Tuberculosis. Karel de Beule, CDTL TMC 207. TMC207-C208 Trial Design. Phase II, placebo-controlled, double-blind Patients with newly diagnosed smear positive MDR-TB

zaide
Download Presentation

Karel de Beule, CDTL TMC 207

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Interim analysis of a double-blind, placebo-controlled study with TMC207 in patients with Multi-Drug Resistant (MDR) Tuberculosis Karel de Beule, CDTL TMC 207

  2. TMC207-C208 Trial Design • Phase II, placebo-controlled, double-blind • Patients with newly diagnosed smear positive MDR-TB • Stratified by trial site and degree of lung cavitation • 2 stage trial design • Stage 1 - Safety and dose determination • 8 weeks dosage TMC207/placebo and BR, then BR and 24 months follow-up • Dose regimen: 400 mg qd for 2 weeks followed by 200 mg three times weekly for 6 weeks • Stage 2 - Recruiting - full 6 month dosage • This presentation is a pre-planned analysis of the stage 1 results after 8 weeks of treatment

  3. Stage 1 Objectives • Primary • Evaluate PK (adequacy of the model predicted exposure) • Evaluate safety and tolerability of TMC207 compared to placebo • Secondary • Evaluate anti-bacterial activity of TMC207at 8 wks vs placebo

  4. Inclusion/Exclusion Criteria • Male and female 18-65 years • Positive sputum smear > 1+ • Confirmed resistance to H and R • HIV negative or HIV+ with CD4+ > 300 and no ART • No previous 2nd line anti-tuberculosis agents • No significant extrapulmonary TB or concomitant illness

  5. Demographics

  6. Background Regimen

  7. PK of TMC207 vs model predictions CONFIDENTIAL RESULTS ONLY FOR UK-CAB MEETING

  8. Most frequent Adverse Events CONFIDENTIAL RESULTS ONLY FOR UK-CAB MEETING

  9. Safety CONFIDENTIAL RESULTS ONLY FOR UK-CAB MEETING

  10. Microbiology parameters • Weekly sputum collection - culture conversion in liquid media • Defined as 2 consecutive negative cultures at least 1 week apart • Drug carry-over effects were prevented • Analysis set = 44 patients (3 withdrawals) • Serial sputum colony counting (SSCC) performed in 22 patients in overnight sputum collections

  11. Culture conversion in liquid media CONFIDENTIAL RESULTS ONLY FOR UK-CAB MEETING

  12. Mean log10 CFU count over time CONFIDENTIAL RESULTS ONLY FOR UK-CAB MEETING

  13. Conclusions CONFIDENTIAL RESULTS ONLY FOR UK-CAB MEETING

  14. Acknowledgements • - The patients who participated in our study • - Dr. Andreas Diacon and team, Stellenbosch University, Cape Town • - Dr. Alexander Pym and team Medical Research Council, Durban • - Dr. Martin Grobusch and team, University of the Witwatersrand • - Dr. Martin Bogoshi and team, Aurum Health, South Africa • - Dr. Renée Krause, C. Pistorius and team, QdotPharma, South Africa • -Members of the TMC207 compound development and clinical teams, Tibotec, Yardley, PA (USA) and Mechelen, Belgium.

More Related