Suggested remit: To appraise the clinical and cost effectiveness of zuranolone within its marketing authorisation for treating severe postnatal depression.

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:
STA Standard
ID number:
6431

Project Team

Project lead
Jeremy Powell

Email enquiries

If you have any queries please email [email protected]


External Assessment Group:
Bristol Technology Assessment Group, University of Bristol

Stakeholders

Companies sponsors
Biogen (zuranolone)
Others
Department of Health and Social Care
 
NHS England
Professional groups
College of Mental Health Pharmacy
 
Royal College of Physicians
 
UK Clinical Pharmacy Association
Associated public health groups
Public Health Wales
 
UK Health Security Agency
Comparator companies
Accord Healthcare (amitriptyline, citalopram, duloxetine, escitalopram, imipramine, lofepramine, mirtazapine, fluoxetine, paroxetine, quetiapine, sertraline and venlafaxine) CAU not received- not participating
 
Amneal Pharma Europe (duloxetine, paroxetine) CAU not received- not participating
 
Arristo Pharma (quetiapine) CAU not received- not participating
 
AstraZeneca (quetiapine) CAU not received- not participating
 
Aurobindo Pharma (citalopram, duloxetine, escitalopram, fluoxetine, mirtazapine, paroxetine, quetiapine, sertraline and venlafaxine) CAU not received- not participating
 
Chiesi (venlafaxine) CAU not received- not participating
 
Consilient Health (duloxetine, escitalopram, quetiapine and venlafaxine) CAU not received- not participating
 
Creo Pharma (lofepramine and trazodone) CAU not received- not participating
 
Dexcel Pharma (venlafaxine) CAU not received- not participating
 
Dr Reddys Labs (duloxetine, fluoxetine and sertraline) CAU not received- not participating
 
Fontus heath (quetiapine) CAU not received- not participating
 
GlaxoSmithKline (paroxetine) CAU not received- not participating
 
HBS Healthcare (duloxetine) CAU not received- not participating
 
Kyowa Kirin (phenelzine) CAU not received- not participating
 
Lilly UK (duloxetine and fluoxetine) CAU not received- not participating
 
Lundbeck (citalopram, escitalopram, vortioxetine) CAU not received- not participating
 
Lupin (sertraline) CAU not received- not participating
 
Marlborough (doxepin) CAU not received- not participating
 
Merck Sharp & Dohme (mirtazapine) CAU not received- not participating
 
Mylan (citalopram, clomipramine, escitalopram, fluoxetine, fluvoxamine, lofepramine, mianserin, mirtazapine, paroxetine, quetiapine, trazodone and venlafaxine) CAU not received- not participating
 
Par Laboratories Europe (fluoxetine) CAU not received- not participating
 
Pfizer (reboxetine, sertraline and venlafaxine) CAU not received- not participating
 
Rivopharm (citalopram, trazodone) CAU not received- not participating
 
Sandoz (citalopram, paroxetine and quetiapine) CAU not received- not participating
 
Servier (agomelatine) CAU not received- not participating
 
SilverCloud (Space from Depression) CAU not received- not participating
 
Sun Pharmaceuticals (sertraline and venlafaxine) CAU not received- not participating
 
Teva UK (amitriptyline, citalopram, clomipramine, fluoxetine, fluvoxamine, imipramine, lofepramine, mianserin, mirtazapine, paroxetine, sertraline, trazodone and venlafaxine) CAU not received- not participating
 
Wockhardt (amitriptyline, fluoxetine, fluvoxamine, mirtazapine and venlafaxine) CAU not received- not participating
 
Zentiva (citalopram, duloxetine, escitalopram, quetiapine, trazodone and trimipramine) CAU not received- 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
28 August 2025 - 18 September 2025 Draft guidance: 1
06 August 2025 Committee meeting
06 August 2025 Declaration of interests
09 January 2025 Invitation to participate
11 November 2024 (14:00) Scoping workshop
16 September 2024 - 14 October 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6431
16 September 2024 In progress. Scoping commencing
07 June 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