polyneuropathy

CHMP meeting highlights – April 2025

28 April 2025 | By Catherine Eckford (European Pharmaceutical Review)

The Committee for Medicinal Products for Human Use (CHMP) recommended approval of a variety of new medicines, including several treatments for hereditary and rare conditions.

news

Topline results show eplontersen slows disease progression in polyneuropathy patients

24 June 2022 | By Sarah Wills (European Pharmaceutical Review)

Data in the NEURO-TTRansform study demonstrates that eplontersen had a positive impact on disease progression, including improvement in neuropathy impairment and quality of life in a substantial number of patients.

news

EMA recommends marketing authorisation to Tegsedi for hereditary transthyretin amyloidosis

7 June 2018 | By European Pharmaceutical Review

The EMA has recommended granting a marketing authorisation for Tegsedi, a medicine for the treatment of stage 1 or stage 2 polyneuropathy...

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Recommended

polyneuropathy

CHMP meeting highlights – April 2025

Topline results show eplontersen slows disease progression in polyneuropathy patients

EMA recommends marketing authorisation to Tegsedi for hereditary transthyretin amyloidosis