Osimertinib: 14 agencies, 2016–2026

This page collects every recorded health technology assessment decision for one molecule across the agencies in our archive, and compares them. The comparison is the point: each agency publishes its own verdict, none publishes how that verdict sits against the others.

What the record shows

On the same population the two systems disagree outright: SMC (Scotland) recorded restricted for “The treatment of adult patients with locally advanced or metastatic epidermal growth factor receptor (EGFR) T790M mutation-positive non-small-cell lung cancer (NSCLC).”, while PBAC (Australia) recorded not recommended for “Locally advanced (Stage III) or metastatic (Stage IV) epidermal growth factor receptor (EGFR) T790M mutation positive non-small cell lung cancer (NSCLC)”.

Assessment has run over 10 years, from 5 May 2016 at AWMSG (Wales) to 21 May 2026 at NICE (England).

ZIN (Netherlands) changed its position: not recommended on 7 Nov 2018, restricted by 15 Apr 2026, after a resubmission.

Every one of the eight highest-volume agencies in this archive has a record for osimertinib.

The file is active: 29 of 65 records date from 2023 or later.

The programme is broad: 15 distinct indication wordings are recorded for osimertinib by the agencies that label one in English (AWMSG, NICE, PBAC and SMC).

8 of these 65 records carry a year of decision but no day, so any interval quoted here is approximate to within a year.

AWMSG (Wales) was first to assess osimertinib, on 5 May 2016; CIPM (Spain) did not open a file until 7 Jul 2022 — a wide spread of 6.2 years between the earliest and latest system to look at it.

The record arrives in waves: 11 separate years each carry two or more decisions, spread across 11 years in total.

13 of the 14 agencies here assessed osimertinib more than once, PBAC (Australia) most often at 8 entries — repeat review is the norm for this molecule rather than the exception.

osimertinib has been through 14 of the 18 agencies in this archive — among the most widely assessed molecules on file.

The full ledger for osimertinib reads 30 recommended, 10 restricted, 8 not recommended and 5 deferred to NICE, with 12 in other categories.

Decisions on file

AgencyDateIndication as recorded OutcomeSource
AWMSG (Wales)29 Apr 2026Maintenance treatment of locally advanced, unresectable, EGFR mutation-positive non-small cell lung cancer (NSCLC) in ad…excluded, NICE appraisedsource
ZIN (Netherlands)15 Apr 2026Advies - alleen vergoeden na prijsdaling osimertinib (Tagrisso®) in combinatie met pemetrexed en chemotherapie voor de b…reimburse only after price negotiation (sluis)source
SMC (Scotland)13 Apr 2026For treatment of adult patients with locally advanced, unresectable NSCLC whose tumours have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations and whose di…acceptedsource
NYE METODER (Norway)15 Mar 2026Kombinasjon med pemetreksed og platinabasert kjemoterapi som førstelinjebehandling hos voksne pasienter med avansert NSC…introducedsource
DMC (Denmark)29 Oct 2025Voksne patienter med lokalt avanceret, inoperabel NSCLC, hvis tumorer har EGFR-exon 19-deletioner eller exon 21 (L858R) …Ikke anbefaletsource

60 further decisions for osimertinib, across 14 agencies, are not shown here. They include the most recent record on file, 21 May 2026 from NICE (England); its outcome is in the subscriber dataset. They link to 48 further source documents.

Related molecules

Coverage: 65 decisions for osimertinib from 14 agencies, 2016 to 2026. Data to 7 Sep 2026. ATC class L01X — Antineoplastics. How this page is produced. Compiled by Altima Partners; queries: sales@altimapartners.co.uk.

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