The Beneluxa Initiative identified impactful medicines suitable for joint HTA submission

Products on this list have been selected as they are of interest for a joint HTA only or combined with a joint negotiation to three or more countries within Beneluxa. The list draws from the work under IHSI high impact reports and ongoing products under the scope of the EU HTA Regulation. While some flexibility is needed in the selection of products, Beneluxa countries generally take into account complexity of products and healthcare service impact.

We invite companies with products on this list to contact the Beneluxa secretariat (info@beneluxa.org) to discuss a joint pilot.

Selected list from 2025 High Impact Reports mentioned medicines in the pipeline, in alphabetical order

Product 

Proposed indication, abbreviated

atacicept (SC)

Lupus nephritis

brensocatib (oral)

Non-cystic fibrosis bronchiectasis

camizestrant (oral)

Advanced or metastatic breast cancer

crinecerfont (oral)

Paediatric classic congenital adrenal hyperplasia

CUTX-101 copper histidinate (SC)

Menkes disease

ecopipam (oral)

Tourette Syndrome

glepaglutide (SC)

Short bowel syndrome

golodirsen (IV)

Duchenne muscular dystrophy

marnetegragene autotemcel (IV)

Leucocyte adhesion deficiency type I

mirdametinib (oral)

Neurofibromatosis type 1-associated plexiform neurofibromas

obicetrapib (oral)

Atherosclerotic cardiovascular disease

olezarsen (SC)

Severe familial chylomicronaemia syndrome

resmetirom(oral)

Metabolic dysfunction-associated steatohepatitis

tinlarebant (oral)

Stargardt disease type 1

veligrotug (IV)

Thyroid eye disease

vimseltinib (oral)

Giant cell tumour of tendon sheath

vorasidenib (PO)

Residual or recurrent IDH-mutant grade 2 glioma

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

List of medicines in Joint Clinical Assessment in which Beneluxa member states are involved as (co-) assessor, in chronological order

Product JCA

Proposed indication, abbreviated

Assessors

Estimated Completion date

tovorafenib (oncology)

Paediatric low grade glioma

NCPE (Ireland) & IQWIG (Germany)

May 2026

sasanlimab (oncology)

Treatment of bladder cancer

 ZIN (Netherlands) & DMC (Denmark) 

   July 2026

onasemnogene abeparvovec ZAMZURA® intrathecal (ATMP)*

Spinal muscular atrophy

NCPE (Ireland) & HAS (France)

August 2026

camizestrant (oncology)

Breast cancer

DVSV (Austria) &

RIZIV-INAMI (Belgium

August 2026

ensartinib (oncology)

ALK-positive lung cancer

DVSV (Austria) & AEMPS (Spain)

End 2026

zopagogene imadenovec (ATMP)

Respiratory papillomatosis

DMC (Denmark) & AiHTA (Austria)

Feb 2027

sonrotoclax (oncology)

Mantle cell lymphoma

RIZIV-INAMI (Belgium)& TLV (Sweden)

March 2027

 

Source: European Commission (2025) Updated - List of ongoing joint clinical assessments. Available at: https://health.ec.europa.eu/latest-updates/updated-list-ongoing-joint-clinical-assessments-2025-09-02_en (Accessed: 30.01.2026).

*Previously, Beneluxa worked on onasemnogene abeparvovec, ZOLGENSMA®IV in spinal muscular atrophy (different indication)

Last update: 9 February 2026