Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

UK considers gauging latent vCJD infection with tests on all postmortems

This article was originally published in Clinica

Executive Summary

The UK government is considering extending postmortem examinations with tests for variant Creutzfeldt-Jakob disease (vCJD), in order to better gauge the extent of latent infection across the entire population. Concerned that 166 UK deaths to date may not reflect the true prevalence, with the significant risk that this poses to transmission through surgery and blood transfusion, the Department of Health (DoH) wants postmortems to include tests on tissues that are known to accumulate the prion protein responsible for vCJD, such as the spleen and the brain. Some 115,000 postmortems are ordered by coroners every year in England alone. The Coroners' Society for England and Wales has criticised the initiative as "inappropriate", but the Health Protection Agency and DoH are reportedly keen to develop the plans and are assessing the practical and legal implications.

You may also be interested in...



Adalvo Hails First European Launch Of Prolonged-Release Pregabalin

After the drug’s approval for use in neuropathic pain within the EU last December, Adalvo announced the analgesic’s first European launch in Germany.

Alvotech Highlights Lack Of Simponi Rivals As It Delivers Golimumab Results

Alvotech has just become the first company to announce positive topline results from a confirmatory clinical study for a proposed golimumab rival to Simponi and Simponi Aria – and moreover, the firm sees limited competition from other biosimilars on the horizon.

Xbrane Assembles The Troops As FDA Says No To Lucentis Biosimilar

Xbrane Biopharma was riding the crest of a wave with the EU launch of its biosimilar to Lucentis, following years of toil and investment. However, plans to roll out the product in the US will have to be pushed back – likely – into the middle of 2025, following a US FDA complete response letter.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

MT046217

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel