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BioWorld - Saturday, June 20, 2026
Home » Topics » Disease categories and therapies » Neurology/psychiatric

Neurology/psychiatric
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DNA in drug capsules

NICE backs Orchard rare disease drug after further cut to $3.9M list price

Feb. 4, 2022
By Richard Staines
In one of its familiar U-turns, the U.K. National Institute for Health and Care Excellence (NICE) has recommended NHS England should fund a rare disease gene therapy from Orchard Therapeutics plc, considered to be the world’s most expensive drug. The list price for Libmeldy (atidarsagene autotemcel) in England and Wales is £2,875,000 (US$3.9 million), making it the most expensive drug that NICE has ever evaluated.
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University of Tokyo discloses BDNF/NT-3 growth factor receptor activators

Feb. 4, 2022

New T-type calcium channel blockers identified at Sumitomo Dainippon Pharma

Feb. 4, 2022

Researchers present preclinical model of ALS

Feb. 4, 2022

Meta-analysis reveals candidate variants associated with brain traits

Feb. 4, 2022

CIRM grant supports Juvena's preclinical work on JUV-161 for myotonic dystrophy type 1

Feb. 3, 2022

New prolyl endopeptidase inhibitors identified at Accure Therapeutics

Feb. 3, 2022

Sarepta and GenEdit report progress under collaboration for neuromuscular diseases

Feb. 2, 2022

CCR4 mediates postoperative pain through skin dendritic cells

Feb. 2, 2022

Sio Gene drops a program and its CEO

Feb. 1, 2022
By Lee Landenberger
Sio Gene Therapies Inc. is retrenching the business as it terminated the company’s AXO-Lenti-PD license agreement with Oxford Biomedica plc for treating Parkinson’s disease. Also, Sio’s CEO, Pavan Cheruvu, is leaving the company. Sio said it is deprioritizing its Parkinson’s disease program due to several factors, including resource requirements and development timelines “to reach meaningful value inflection for the program and an increasingly challenging market and regulatory environment” for the indication.
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