Garadacimab: where the agencies disagree

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

CIPM (Spain), DMC (Denmark) and G-BA (Germany), among others, recommended or restricted garadacimab, while NYE METODER (Norway) did not recommend it.

Every record falls within a 1.5-year window, 2024 to 28 Jan 2026 — a compressed review cycle.

No assessment is on file from HAS (France) and SMC (Scotland), each among the eight highest-volume agencies here.

The file is active: 9 of 10 records date from 2023 or later.

3 distinct indication wordings are recorded for garadacimab by the agencies that label one in English (AWMSG, NICE and PBAC).

1 of these 10 records carries a year of decision but no day, so any interval quoted here is approximate to within a year.

PBAC (Australia) was first to assess garadacimab, in 2024; CIPM (Spain) did not open a file until 28 Jan 2026 — a moderate spread of 1.5 years between the earliest and latest system to look at it.

Activity is concentrated rather than steady: 6 of 9 dated records fall in 2025 alone.

10 of the 18 agencies in this archive hold a record for garadacimab.

The full ledger for garadacimab reads 6 recommended, 1 restricted, 1 not recommended and 1 appraised, with 1 in other categories.

Decisions on file

AgencyDateIndication as recorded OutcomeSource
TLV (Sweden)27 Jan 2026Andembry ingår i högkostnadsskyddet med begränsningrestricted subsidysource
NYE METODER (Norway)7 Dec 2025For rutinemessig forebygging av residiverende anfall av hereditært angioødem (HAE) hos pasienter ≥12 årnot introducedsource
DMC (Denmark)29 Oct 2025Til rutinemæssig forebyggelse af tilbagevendende anfald af hereditært angioødem (HAE) hos voksne og unge patienter i ald…Direkte indplaceringsource
NICE (England)8 Oct 2025NICE TA1101published appraisalsource
ZIN (Netherlands)26 Aug 2025Advies - vergoed garadacimab (Andembry®) voor de behandeling van hereditair angio-oedeem (HAE)reimbursedsource

5 further decisions for garadacimab, across 5 agencies, are not shown here. They include the most recent record on file, 28 Jan 2026 from CIPM (Spain); its outcome is in the subscriber dataset. They link to 5 further source documents.

Related molecules

Coverage: 10 decisions for garadacimab from 10 agencies, 2024 to 2026. Data to 7 Sep 2026. ATC class B06A — Other hematological agents. How this page is produced. Compiled by Altima Partners; queries: sales@altimapartners.co.uk.

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