Changeflow GovPing Healthcare & Life Sciences Ripretinib Recommended for Advanced GIST After ...
Routine Guidance Amended Final

Ripretinib Recommended for Advanced GIST After Kinase Inhibitors

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Summary

NICE has published final technology appraisal TA1146 recommending ripretinib (Qinlock) for NHS use in adults with advanced gastrointestinal stromal tumours (GIST) who have received three or more kinase inhibitors. This guidance updates and replaces the prior recommendation TA881, reflecting new evidence reviewed on 28 April 2026. NHS commissioners and providers are required to fund ripretinib within three months of the publication date in accordance with NHS Constitution obligations.

“Commissioners and/or providers have a responsibility to provide the funding required to enable the guidance to be applied when individual health professionals and their patients wish to use it, in accordance with the NHS Constitution.”

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About this source

GovPing monitors NICE Technology Appraisals for new healthcare & life sciences regulatory changes. Every update since tracking began is archived, classified, and available as free RSS or email alerts — 12 changes logged to date.

What changed

NICE technology appraisal TA1146 updates prior guidance TA881 by recommending ripretinib for NHS funding in the stated patient population. The guidance includes a simple discount patient access scheme, with commercial details available via the CAP Portal for NHS organisations and through deciphera.com for non-NHS entities.

NHS commissioners and providers should note the three-month funding obligation under the NHS Constitution. Health professionals applying these recommendations must exercise individual judgement in consultation with patients and/or their carers, alongside their obligations under equality and health inequality legislation. Adverse events related to ripretinib should be reported via the MHRA Yellow Card Scheme.

Archived snapshot

Apr 28, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Ripretinib for treating advanced gastrointestinal stromal tumours after 3 or more kinase inhibitors

  • Technology appraisal guidance
  • TA1146
  • Published:

28 April 2026

Download guidance (PDF)

Overview

Evidence-based recommendations on ripretinib (Qinlock) for treating advanced gastrointestinal stromal tumours after 3 or more kinase inhibitors in adults.

Last reviewed: 28 April 2026

This guidance updates and replaces NICE technology appraisal guidance on ripretinib for treating advanced gastrointestinal stromal tumour after 3 or more treatments (TA881).

Next review: This guidance will be reviewed if there is new evidence that is likely to change the recommendations.

Commercial arrangement

There is a simple discount patient access scheme for ripretinib. NHS organisations can get details on the Commercial Access and Pricing (CAP) Portal. Non-NHS organisations can contact marketaccess.gbr@deciphera.com for details.

Guidance development process

How we develop NICE technology appraisal guidance

Your responsibility

The recommendations in this guidance represent the view of NICE, arrived at after careful consideration of the evidence available. When exercising their judgement, health professionals are expected to take this guidance fully into account, alongside the individual needs, preferences and values of their patients. The application of the recommendations in this guidance is at the discretion of health professionals and their individual patients and do not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of the individual patient, in consultation with the patient and/or their carer or guardian.

All problems (adverse events) related to a medicine or medical device used for treatment or in a procedure should be reported to the Medicines and Healthcare products Regulatory Agency using the Yellow Card Scheme.

Commissioners and/or providers have a responsibility to provide the funding required to enable the guidance to be applied when individual health professionals and their patients wish to use it, in accordance with the NHS Constitution. They should do so in light of their duties to have due regard to the need to eliminate unlawful discrimination, to advance equality of opportunity and to reduce health inequalities.

Commissioners and providers have a responsibility to promote an environmentally sustainable health and care system and should assess and reduce the environmental impact of implementing NICE recommendations wherever possible.

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Last updated

Classification

Agency
NICE
Published
April 28th, 2026
Instrument
Guidance
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Substantive
Supersedes
TA881

Who this affects

Applies to
Healthcare providers Pharmaceutical companies NHS organisations
Industry sector
6211 Healthcare Providers 3254 Pharmaceutical Manufacturing
Activity scope
Drug reimbursement decisions Technology appraisal Cancer treatment funding
Geographic scope
United Kingdom GB

Taxonomy

Primary area
Healthcare
Operational domain
Healthcare
Topics
Public Health Pharmaceuticals

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