Suggested remit: To appraise the clinical and cost effectiveness of vibegron within its marketing authorisation for treating symptoms of overactive bladder.
 
Status In progress
Technology type Medicine
Decision Selected
Reason for decision Anticipate the topic will be of importance to patients, carers, professionals, commissioners and the health of the public to ensure clinical benefit is realised, inequalities in use addressed, and help them make the best use of NHS resources
Process Cost Comparison Standard
ID number 6300

Project Team

Project lead Jeremy Powell

Email enquiries

External Assessment Group BMJ Technology Assessment Group (BMJ-TAG), BMJ

Stakeholders

Companies sponsors Pierre Fabre (vibegron)
Others Department of Health and Social Care
  NHS England
Professional groups British Society of Urogynaecology
  Royal College of Physicians
Comparator companies Aristo Pharma (fesoterodine) (CAU not signed - not participating)
  Aspire Pharma (darifenacin, fesoterodine, solifenacin, tolterodine)(CAU not signed - not participating)
  Astellas Pharma (mirabegron, solifenacin)(CAU signed - participating)
  Aurobindo Pharma – Milpharm (solifenacin)(CAU not signed - not participating)
  Brillpharma (oxybutynin)(CAU not signed - not participating)
  Brown & Burk (solifenacin)(CAU not signed - not participating)
  Celix Pharma (fesoterodine, solifenacin)(CAU not signed - not participating)
  Dr. Reddy's Laboratories (fesoterodine)(CAU not signed - not participating)
  Genus Pharmaceuticals (fesoterodine, solifenacin)(CAU not signed - not participating)
  Ennogen Healthcare (propiverine)(CAU not signed - not participating)
  Glenmark Pharmaceuticals (solifenacin, trospium)(CAU not signed - not participating)
  Krka (solifenacin)(CAU not signed - not participating)
  Medical Valley Invest (fesoterodine)(CAU not signed - not participating)
  MSN Laboratories (solifenacin)(CAU not signed - not participating)
  Neon Healthcare (oxybutynin)(CAU not signed - not participating)
  Northumbria Pharma (tolterodine)(CAU not signed - not participating)
  Pfizer (fesoterodine)(CAU not signed - not participating)
  Ranbaxy, a Sun Pharmaceutical Company (solifenacin)(CAU not signed - not participating)
  Roma Pharmaceuticals (oxybutynin)(CAU not signed - not participating)
  Sandoz (solifenacin, tolterodine)(CAU not signed - not participating)
  Strides Pharma (oxybutynin)(CAU not signed - not participating)
  SyriMed (oxybutynin) (CAU not signed - not participating)
  Tillomed Laboratories (oxybutynin, solifenacin)(CAU not signed - not participating)
  Viatris (tolterodine, trospium)(CAU not signed - not participating)
  Zentiva (fesoterodine, oxybutynin, solifenacin, tolterodine)(CAU not signed - not participating)
General commentators All Wales Therapeutics and Toxicology Centre
  British National Formulary
  Department of Health - Northern Ireland
  Healthcare Improvement Scotland
  Medicines and Healthcare products Regulatory Agency
  Scottish Medicines Consortium
  Welsh Government
  Welsh Health Specialised Services Committee

Timeline

Key events during the development of the guidance:

Date Update
01 March 2024 Invitation to participate
12 September 2023 - 10 October 2023 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6300
03 August 2023 In progress. DHSC referral received
15 May 2023 Awaiting development. Status change linked to Topic Selection Decision being set to Selected

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