Atrasentan for hormone refractory prostate cancer
Following on from information provided to NICE by the company in May 2018, the appraisal of Atrasentan for hormone refractory prostate cancer [ID390] 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 390
Referral date 01 June 2004
Topic area
  • Cancer
  • Urogenital

Provisional Schedule

Closing date for invited submissions / evidence submission: TBC
1st appraisal committee meeting: TBC
2nd appraisal committee meeting TBC

Project Team

Assessment Group / Evidence Review Group: TBC
Communications manager: TBC
Executive Lead: TBC
Project manager: TBC
Technical Lead: TBC

Email enquiries

Timeline

Key events during the development of the guidance:

Date Update
31 October 2022 Discontinued. Following on from information provided to NICE by the company in May 2018, the appraisal of Atrasentan for hormone refractory prostate cancer [ID390] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
27 May 2005 Topic summary published
25 August 2006 This topic was transferred to the Single technology appraisal (STA) process as part of the Institute's 12th wave work programme.
8 January 2007 Topic is suspended as the manufacturer has not applied for EMEA regulatory approval at this time

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