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Epcoritamab with rituximab and lenalidomide for treating relapsed or refractory follicular lymphoma after 1 or more systemic treatments [ID6586]

  • In development
  • Reference number: GID-TA11768
  • Expected publication date:  28 October 2026
  • Project information
  • Project documents

On this page

  1. Invitation to participate
  2. Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
  3. Notes

Documents

Documents created during the development process.

Invitation to participate

  • Final scope (PDF 156 KB)

    Published:
    24 November 2025
  • Final stakeholder list (PDF 148 KB)

    Published:
    24 November 2025
  • NICE's response to comments on the draft scope and provisional stakeholder list (PDF 207 KB)

    Published:
    24 November 2025
  • Equality impact assessment (scoping) (PDF 108 KB)

    Published:
    24 November 2025

Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators

  • Draft scope post referral (PDF 165 KB)

    Published:
    18 September 2025
  • Provisional stakeholder list post referral (PDF 154 KB)

    Published:
    18 September 2025

Notes

  • To appraise the clinical and cost effectiveness of Rituximab + Lenalidomide + Epcoritamab within its marketing authorisation for treating follicular lymphoma

  • This appraisal has been delayed and will now be considered by the NICE Technology Appraisal Committee at a meeting on Tuesday 8 September 2026.

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