Statement on the Joint Action 3 Prolongation

EUnetHTA Joint Action 3 has received official approval from Consumers, Health, Agriculture and Food Executive Agency (CHAFEA) for an extension of an additional 12 months without additional funding. This prolongation is meant to allow the finalisation of outstanding deliverables and, where possible, further prepare for a future European HTA system. The Executive Board is currently […]

EUnetHTA 2020 Assembly – Welcome Guide now available

The annual EUnetHTA Assembly aims to provide an overview into the year’s activity, while stimulating discussion on HTA-related topics and looking to the network’s next steps and future developments. Due to current events, we will be holding the 1st April Assembly online with network members, while this year’s Forum is postponed till a later date. […]

EUnetHTA Response to COVID-19

We all are faced with an unprecedented situation, a reminder of how fragile we as individuals are, how fragile our societies remain. EUnetHTA is a network of specialists, dedicated in their own jurisdictions to excellence and the support of their individual health care systems. EUnetHTA derives its strength from its diversity, from the ability to […]

PTJA09 – Brolucizumab for the treatment of adults with neovascular (wet) age-related macular degeneration (AMD)

This is the pharmaceutical Joint Assessment PTJA09 on brolucizumab. In February 2020, the European Commission granted marketing authorisation for Beovu® (brolucizumab) for the treatment of adults with neovascular (wet) AMD. This Joint Assessment aims to compare the clinical effectiveness and safety of brolucizumab in the target patient population with relevant comparators according to the national […]

EUnetHTA releases a new guidance document that supports health technology assessments: “Practical considerations when critically assessing economic evaluations”

The aim of this guidance document is to pass on some knowledge and know-how to all stakeholders with an interest in economic evaluations by providing an overview of important points for consideration when performing/assessing such evaluations, supported by a selection of real-world examples. About this document: Authoring team: Mattias Neyt (KCE, Belgium); Martin Eriksson (SBU, […]

Statement from the EUnetHTA Secretariat on COVID-19

Due to the developing COVID-19 scenario affecting Europe and with regard to the policy responses emerging on a per national basis from certain areas, the EUnetHTA Secretariat is implementing precautionary changes to its planned 2020 events schedule. This is following instructions from the Executive Board of the Dutch National Healthcare Institute (ZIN) to revise plans […]

EUnetHTA Magazine – Winter 2020 – Now Available

We are pleased to publish the Winter 2020 issue of EUnetHTA Magazine, our quarterly update on HTA with input from network stakeholders. As always, we welcome your feedback so we can continue to improve how we can focus on developments in HTA. Happy reading! Click here for more.  

PTJA05 – enasidenib for the treatment of adult patients with relapsed or refractory acute myeloid leukaemia (AML) with an isocitrate dehydrogenase 2 (IDH2) mutation

On 6 Dec 2019, Celgene officially notified the Committee for Medicinal Products for Human Use (CHMP) that it wishes to withdraw its application for a marketing authorisation for enasidenib. Since no CHMP opinion will be granted at this stage, EUnetHTA closed this Joint Assessment on 12 Dec 2019. The final Project Plan for the applied […]

OTCA21 Updated Final Project Plan and related documents now available

EUnetHTA is pleased to announce that the final project plan, now updated with new dates for publication of the final report, and comments from external experts and manufacturers for the Other Technologies Collaborative Assessment OTCA21 “Hypoglossal nerve stimulation systems for treatment of obstructive sleep apnoea” are now available for access. Please access  at the following […]

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