MHRA
- Local brand name: Bortezomib Hospira
- Status: approved
NICE has issued 13 UK HTA decisions
13 decisions from NICE for Velcade in United Kingdom.
NICE recommended Velcade for the treatment of previously treated multiple myeloma. This decision was made based on a commercial arrangement, which suggests that a patient access scheme was in place to make the treatment more affordable. No restrictions were placed on the use of Velcade.
NICE recommended Velcade for the treatment of multiple myeloma. This decision was made for the indication of induction therapy before high-dose chemotherapy and autologous stem cell transplantation. No cost basis was reported, and no restriction or condition was applied.
NICE recommended Velcade for the first-line treatment of multiple myeloma. This decision was made without a Patient Access Scheme or commercial arrangement. No restrictions were placed on the use of Velcade.
NICE recommended Velcade for the treatment of relapsed multiple myeloma. This decision was made without a reported cost-effectiveness analysis or a Patient Access Scheme. No commercial arrangement or restriction was applied to the recommendation.
NICE recommended Velcade for the treatment of multiple myeloma in patients who have previously received lenalidomide and bortezomib. This decision was made based on a commercial arrangement and a patient access scheme. No restrictions were placed on the use of Velcade.
NICE recommended Velcade for the treatment of previously treated multiple myeloma. This decision was made based on a commercial arrangement and a Patient Access Scheme. No restrictions were placed on the use of Velcade.
NICE made a decision to terminate the appraisal of Velcade for the treatment of untreated multiple myeloma. This decision means that the appraisal process for Velcade in this indication has been stopped. The decision was made without a recommendation on the cost-effectiveness of Velcade, as the appraisal was terminated.
NICE made a decision to terminate the appraisal of Velcade for the treatment of untreated multiple myeloma. This decision means that the appraisal process for Velcade in this indication has been stopped. The decision was made without a recommendation on the cost-effectiveness of Velcade, as the appraisal was terminated.
NICE recommended Velcade for the treatment of previously treated multiple myeloma. The decision was made based on a commercial arrangement. No restriction or condition was placed on the use of Velcade.
NICE made a decision to terminate the appraisal of Velcade for treating relapsed or refractory multiple myeloma. This decision means that the appraisal process for Velcade in this indication has been stopped. The decision was made without a recommendation on the cost-effectiveness of Velcade, as the appraisal was terminated.
NICE recommended Velcade for the treatment of multiple myeloma in patients who have previously received bortezomib. This decision was made based on a commercial arrangement, indicating that the manufacturer agreed to a specific price or terms for the drug. There were no restrictions or conditions placed on the use of Velcade for this indication.
NICE made a decision to terminate the appraisal of Velcade for treating multiple myeloma after second or subsequent relapse. This decision was made without a recommendation on the cost-effectiveness of the treatment. The appraisal was terminated, which means that NICE did not make a recommendation on the use of Velcade for this indication.
NICE recommended Velcade for the treatment of previously untreated mantle cell lymphoma. This decision was made without a Patient Access Scheme or commercial arrangement. No restrictions were placed on the use of Velcade for this indication.
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. MHRA has authorised it.
Shilpa is the originator. The local marketing authorisation holder may differ — check the official source linked above.
Yes — 13 UK HTA decisions on record from NICE.