Hepatitis C (chronic) - ombitasvir/paritaprevir/ritonavir (with or without dasabuvir): committee papers B
Table of contents
09 - Evidence Review Group report prepared by Southampton Health Technology Assessments Centre (SHTAC)
10 - Evidence Review Group response to company factual accuracy check
11 – Evidence Review Group report erratum
12 – Evidence Review Group additional analyses
13 – NICE specification letter to company requesting further work
14 – Company additional analyses from AbbVie
15 – Evidence Review Group commentary on company additional analyses
16 – Addendum to Evidence Review Group commentary on company additional analyses
17 – Marketing Authorisation clarification received from the European Medicines Agency (EMA)
18 – NHS England comments received on the ACD for ledipasvir-sofosbuvir for treating chronic hepatitis C
19 – NICE request to NHS England for clarification on hepatitis C drugs
20 – NHS England clarification response
21 – Consultee response – AbbVie
22 – Consultee response – The Hepatitis C Trust
23 – Consultee response - British HIV Association (BHIVA) and the British Association of Sexual Health and HIV (BASHH)
24 – Consultee response – The British Society of Gastroenterology (BSG), British Viral hepatitis Group (BVHG), British Association for the Study of the Liver (BASL) and Royal College of Pathologists
25 – Consultation response – Royal College of Physicians
26 – Consultee response – United Kingdom Clinical Pharmacy Association (UKCPA)
27 – Consultee response – Foundation for Liver Research
28 – Patient expert response from Gore
Hepatitis C (chronic) - ombitasvir/paritaprevir/ritonavir (with or without dasabuvir): committee papers B
29 July 2015 (6.95 Mb 34 sec) |
This page was last updated: 29 July 2015