1 / 19

Global Plan to STOP TB: Diagnostics WG

Global Plan to STOP TB: Diagnostics WG . Jane Cunningham Medical Officer WHO/TDR/PDE Secretariat STOP TB Diagnostics Working Group. The Global Plan Process….

libby
Télécharger la présentation

Global Plan to STOP TB: Diagnostics WG

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. Global Plan to STOP TB: Diagnostics WG Jane Cunningham Medical Officer WHO/TDR/PDE Secretariat STOP TB Diagnostics Working Group

  2. The Global Plan Process…. • Planning workshop in Montreux Switzerland attended by the WG chair, secretariat and the WG Chair appointed focal point, Heidi Albert, Biotec Labs. • The aim was to model the collective impact of proposed WG activities, assess whether the impact would be sufficient to meet the global TB targets for 2015, and estimate the costs involved

  3. The Global Plan Process…. • # 1 --- Understand the MODEL !!! • # 2--- Teach modelers about DIAGNOSTICS !!! • # 3 -- Estimate costs for R&D and implementation of diagnostics that don't exist !!!

  4. births immunized, R transmission uninfected, U primary TB latent TB infected: latent, L exogenous + endogenous exogenous + endogenous good treatment? smear conversion? TB deaths infectious TB, I non-infectious TB, N TB deaths natural cure + good treatment relapse? natural cure, R Mechanisms

  5. The Global Plan Process…. • # 1 --- Understand the MODEL !!! • # 2--- Teach modelers about DIAGNOSTICS !!! • # 3 -- Estimate costs for R&D and implementation of diagnostics that don't exist !!!

  6. Purpose Test Indications Case Detection Drug susceptibility testing Latent TB Infection • Detect pulmonary TB with high bacterial load (SS+) • Detect pulmonary TB with low bacterial load (SS -, Cx +) • Detect extra-pulmonary and pediatric TB • Detect MDR-TB for treatment • Detect MDR-TB for surveillance • Detect LTBI for surveillance • Detect LTBI for treatment Sensitivity (HIV+, pulm, e-p); sm+cases averted; overtreatment averted

  7. Targets for Test Introduction Leading to Sustainable Adoption: 2006-2015

  8. Working Group and Secretariat Strategic Plans • In October 2004, the Coordinating Board asked each WG (plus the Partnership Secretariat) to provide by the end of April 2005 its draft strategic plan of activities and budgets necessary to contribute to achieving the 2015 global TB control targets. • 1st draft circulated in April/May 2005 • Final version – September 2005

  9. Highlights of the Strategic Plan • Vision: to develop and introduce cost-effective and appropriate new diagnostic tools that are accessible to patients and will contribute towards improved control of the global TB epidemic and improve the quality of patient care. • Ideal toolbox would contain diagnostic technologies, all of which perform equally well in HIV-infected subjects, to: • improve TB case detection both through high sensitivity/specificity and improved accessibility – simple, accurate, inexpensive, same day, near-patient products are the ultimate goal • rapidly and inexpensively identify drug resistant TB disease, enabling timely effective patient treatment to reduce both individual morbidity and continuing transmission • reliably identify latent TB infection and define the risk of future progression to active disease, enabling rational use of preventive therapy in appropriate subjects

  10. Objectives • OBJECTIVE 1: Address existing knowledge gaps obstructing development of new diagnostic tools • OBJECTIVE 2: Development and evaluation of a portfolio of new diagnostic tools and demonstration of impact • OBJECTIVE 3: Implementation of new diagnostic tools and ensuring access

  11. TB Diagnostics Development Pipeline: 2005

  12. Objective 1: Targets & Indicators • Discovery science to identify new markers (also in HIV-infected subjects) with improved discriminative power for active disease (may be antigenic, immunological, proteomic or other) and drug resistance • Indicators: # of grants; publications; targets/reagents, new technologies, sample requests from reference banks

  13. Objective 2: Targets & Indicators • Inclusion of related goals in research funding calls by major funding agencies • Public sector product development agreements with industry • Coordinated evaluation and demonstration projects Indicators: # of - funding opportunities; Product Development agreements with industrial partners; successfully completed Development and Technical Evaluations according to Product Specifications; clinical evaluation and demonstration sites developed and authorized; peer-reviewed publications reporting results from evaluation projects

  14. Targets for Test Introduction Leading to Sustainable Adoption: 2006-2015

  15. Objective 3: Targets & Indicators • Operational studies to demonstrate epidemiological and economic impact of new tools in high-burden settings • Accelerated registration of products with proven utility • National and international policy changes reflecting impact evidence on new diagnostics • Creation of demand through communication to stakeholders (NTPs, MOH, technical and funding agencies.) • Ensured access to proven technologies through inclusion in GDF or other procurement mechanisms Key Indicators: # of NTPs with new diagnostics in policy recommendations and # implemented at district, local and point of care Modeling studies ---- FIND Symposium – October 21,2005

  16. Key Risk Factors • Insufficient financial investment and timing of investment • Technologies Fail • Inadequate development of laboratory strengthening • Impaired access to new products • Interrupted product supply

  17. Acknowledgements: Heidi Albert David Moore Mark Perkins Afranio Kritski Ruth McNerney Arend Kolk Chris Dye Andrea Pantoja Bernadette Bourdin

More Related