Status:
Topic selection
Technology type:
Medicine
Decision:
Not selected
Reason for decision:
Not eligible for Health Technology Evaluation guidance
Further information:
The 2024 voluntary scheme for branded medicines, pricing, access and growth states that NICE will continue to evaluate all new active substances and significant indications, except where there is a clear rationale not to do so. Decision makers have concluded that the clear rationale to not evaluate this product is due to Subcutaneous pembrolizumab being a new formulation of existing guidance TA531, TA683 and TA770. Therefore, there would be no additional value in conducting a separate evaluation. Please see eligibility criteria within the prioritisation manual for further information.
ID number:
12213

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For further information on how we select topics for development, please see our page about prioritising our guidance topics