MHRA
- Local brand name: Herceptin
- Status: approved
NICE has issued 15 UK HTA decisions
15 decisions from NICE for Herceptin in United Kingdom.
NICE made a decision to terminate the appraisal of Herceptin for treating hormone receptor-positive HER2-low metastatic breast cancer after 2 or more endocrine treatments. This decision means that NICE will not make a recommendation on the use of Herceptin for this specific indication. The cost-effectiveness of Herceptin was not reported as part of this decision.
NICE made a decision not to recommend Herceptin for treating HER2-low metastatic or unresectable breast cancer after chemotherapy. This decision was made without a reported cost-effectiveness analysis or a patient access scheme. No commercial arrangement was considered.
NICE made a decision not to recommend Herceptin for the treatment of untreated locally advanced unresectable or metastatic HER2-positive gastric or gastro-oesophageal junction adenocarcinoma. This decision was made without a reported cost-effectiveness analysis, as the ICER was not provided. There were no restrictions or conditions placed on the use of Herceptin for this indication.
NICE made a decision to terminate the appraisal of Herceptin for treating HER2-mutated advanced non-small-cell lung cancer after platinum-based chemotherapy. This decision means that NICE will not make a recommendation on the use of Herceptin for this specific indication. The decision to terminate the appraisal was made without a recommendation on the cost-effectiveness of Herceptin, as the cost basis is not reported.
NICE made a decision to terminate the appraisal of Herceptin for treating HER2-positive unresectable or metastatic gastric or gastro-oesophageal junction cancer. 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 final decision on the use of Herceptin for this indication.
NICE recommended Herceptin for treating HER2-positive unresectable or metastatic breast cancer after 1 or more anti-HER2 treatments. This decision was made based on a commercial arrangement and a Patient Access Scheme. No restrictions were placed on the use of Herceptin.
NICE recommended Herceptin for treating HER2-positive advanced breast cancer after 2 or more anti-HER2 therapies. This decision was made based on a commercial arrangement and a patient access scheme. No restrictions were placed on the use of Herceptin.
NICE recommended Herceptin for treating HER2-positive unresectable or metastatic breast cancer after 2 or more anti-HER2 therapies, but with restrictions. This decision was made with the conditions of a managed access agreement in place. The use of Herceptin is only recommended if these conditions are followed.
NICE recommended Herceptin for the adjuvant treatment of HER2-positive early breast cancer. This decision was made based on a commercial arrangement, indicating that the manufacturer agreed to a specific price or reimbursement terms. There were no restrictions or conditions placed on the use of Herceptin for this indication.
NICE recommended Herceptin for the extended adjuvant treatment of hormone receptor-positive, HER2-positive early stage breast cancer after adjuvant trastuzumab. This decision was made based on a commercial arrangement, indicating that the manufacturer agreed to a specific price or reimbursement terms. There were no restrictions or conditions placed on the use of Herceptin for this indication.
NICE recommended Herceptin for treating HER2-positive breast cancer. This decision was made without a reported cost-effectiveness analysis. There were no restrictions or conditions placed on the use of Herceptin.
NICE recommended Herceptin for treating HER2-positive advanced breast cancer after trastuzumab and a taxane. This decision was made based on a commercial arrangement and a Patient Access Scheme. No restrictions were placed on the use of Herceptin.
NICE did not recommend Herceptin for the first-line treatment of metastatic hormone receptor-positive breast cancer that overexpresses HER2. This decision was made without a reported cost-effectiveness analysis or consideration of a Patient Access Scheme or commercial arrangement. No restrictions were placed on the use of Herceptin for this indication.
NICE recommended Herceptin for the treatment of HER2-positive metastatic gastric cancer. This decision was made without a specific cost basis being reported. There were no restrictions or conditions placed on the use of Herceptin for this indication.
NICE recommended Herceptin for the treatment of advanced breast cancer. 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.
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. MHRA has authorised it.
Roche is the originator. The local marketing authorisation holder may differ — check the official source linked above.
Yes — 15 UK HTA decisions on record from NICE.