Faldaprevir for treating genotype 1 chronic hepatitis C
Please note that following on from information provided to NICE by the company in June 2014, the appraisal of Faldaprevir for treating genotype 1 chronic hepatitis C [ID670] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
 
Status Discontinued
Technology type Medicine
Decision Selected
Process TA
ID number 670
Referral date 01 February 2014
Topic area
  • Digestive system
  • Infectious diseases

Provisional Schedule

Closing date for invited submissions / evidence submission: TBC
1st appraisal committee meeting: TBC

Project Team

Communications manager: TBC
Executive Lead: TBC
Project manager:

Jeremy Powell

Technical Lead: TBC

Email enquiries

Timeline

Key events during the development of the guidance:

Date Update
23 January 2023 Discontinued. Please note that following on from information provided to NICE by the company in June 2014, the appraisal of Faldaprevir for treating genotype 1 chronic hepatitis C [ID670] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
09 July 2014 The manufacturer of faldaprevir, Boehringer Ingelheim, has informed us that it has decided not to proceed with the development of faldaprevir for treating hepatitis C. Boehringer Ingelheim has re-evaluated its strategy in hepatitis C, and considers that there are now several new treatment options available for patients and that there is no longer an unmet medical need that would be filled with its faldaprevir interferon-based regimen

For further information on our processes and methods, please see our CHTE processes and methods manual