HTA ID Drug Brand Indication Assessment status Date
- Vandetanib Caprelsa® For the treatment of aggressive and symptomatic medullary thyroid cancer (MTC) in patients with unresectable locally advanced or metastatic disease. Rapid review complete 4th July 2013
- Vedolizumab Entyvio® For the treatment of adult patients with moderately to severely active Crohn’s disease who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a tumour necrosis factor-alpha (TNFα) antagonist. Assessment process complete 13th November 2015
- Vedolizumab Entyvio® For the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a tumour necrosis factor-alpha (TNFα) antagonist. Assessment process complete 13th November 2015
20029 Vedolizumab Entyvio® For subcutaneous administration is indicated for the treatment of adult patients with moderately to severely active Crohn’s disease who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or an anti-TNFα. Rapid review complete 12th August 2020
20030 Vedolizumab Entyvio® For subcutaneous administration is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or an anti-TNFα. Rapid review complete 12th August 2020
- Velaglucerase Alfa VPRIV® For long-term enzyme replacement therapy (ERT) in patients with type1 Gaucher disease. Rapid review complete 20th June 2011
- Vemurafenib Zelboraf® For the treatment of adult patients with BRAF V600 mutation-positive unresectable or metastatic melanoma. Assessment process complete 3rd September 2012
- Venetoclax Venclyxto® For the treatment of chronic lymphocytic leukaemia (CLL) Rapid review complete 21st June 2018
22001 Venetoclax Venclyxto® In combination with a hypomethylating agent is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (AML) who are ineligible for intensive chemotherapy. NCPE Assessment Process Complete 5th June 2024
20046 Venetoclax in combination with obinutuzumab Venclyxto® / Gazyvaro® For the treatment of adult patients with previously untreated chronic lymphocytic leukaemia. Assessment process complete 17th August 2021
- Venetoclax Venclyxto® For the treatment of adult patients with CLL who have received at least one prior therapy. Assessment process complete 8th November 2019
21027 Vericiguat Verquvo® For the treatment of symptomatic chronic heart failure in adult patients with reduced ejection fraction who are stabilised after a recent decompensation event requiring intravenous therapy. NCPE Assessment Process Complete 15th July 2021
- Vernakalant Brinavess® For haemodynamically stable, symptomatic patients with atrial fibrillation of less than 48 hours duration. Assessment process complete 4th May 2011
- Vestronidase alfa MEPSEVII® For the treatment of non-neurological manifestations of MPS VII. Rapid review complete 22nd May 2019
24043 Vibegron Obgemsa® Vibegron (Obgemsa®) is indicated for the symptomatic treatment of adult patients with overactive bladder syndrome. Rapid Review Complete 26th November 2024
- Vismodegib Erivedge® For the treatment of adult patients with locally advanced basal cell carcinoma inappropriate for surgery or radiotherapy or metastatic basal cell carcinoma. Assessment process complete 22nd January 2014
23003 Voclosporin Lupkynis® Voclosporin is indicated in combination with mycophenolate mofetil for the treatment of adult patients with active class III, IV or V (including mixed class III/V and IV/V) lupus nephritis (LN). NCPE Assessment Process Complete 5th December 2024
19041 Voretigene neparvovec Luxturna® For the treatment of adult and paediatric patients with vision loss due to inherited retinal dystrophy caused by confirmed biallelic RPE65 mutations and who have sufficient viable retinal cells. NCPE Assessment Process Complete 20th October 2023
- Vortioxetine Brintellix® For the treatment of major depressive episodes in adults. Assessment process complete 18th November 2016
22028 Vosoritide Voxzogo® For the treatment of genetically confirmed achondroplasia in patients aged two years and older whose epiphyses are not closed. NCPE Assessment Process Complete 5th October 2023
23035 Vutrisiran Amvuttra® Indicated for the treatment of hereditary transthyretin-mediated amyloidosis (hATTR amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy Rapid Review complete 5th June 2024