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BioWorld - Monday, August 3, 2026
Home » Topics » Neurology/psychiatric, BioWorld

Neurology/psychiatric, BioWorld
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Man piecing together a puzzle
CTAD 2019

Key for aducanumab success: higher dose, longer exposure

Dec. 5, 2019
By Brian Orelli
SAN DIEGO  – Following up on its October announcement that it would file for FDA approval of beta-amyloid-targeting aducanumab, Biogen Inc. presented the final dataset for the phase III Emerge and Engage studies at the 12th Clinical Trials on Alzheimer’s Disease Meeting.
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CTAD 2019

Worth the wait, Acadia’s Nuplazid looks good in dementia-related psychosis

Dec. 5, 2019
By Brian Orelli
SAN DIEGO – Three months ago, Acadia Pharmaceuticals Inc. said Nuplazid (pimavanserin), its serotonin inverse agonist and antagonist that preferentially targets the 5-HT2A receptor, met the primary endpoint during an interim look at the phase III Harmony study in patients with dementia-related psychosis (DRP).
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Neurocrine, Xenon in deal for $50M up front, up to $1.7B in milestones

Dec. 2, 2019
By Lee Landenberger
In its second large deal of the calendar year, Neurocrine Biosciences Inc. acquired the rights to Xenon Pharmaceutical Inc.’s selective sodium channel inhibitor for treating epileptic encephalopathy. Xenon receives $30 million up front, $20 million in equity and up to $1.7 billion in potential development, regulatory and commercial milestone payments.
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Supernus' non-superlative ADHD try vexing investors, still promise in SPN-812

Nov. 7, 2019
By Randy Osborne
Supernus Pharmaceuticals Inc. CEO Jack Khattar said the phase III failure in the study called P301 with SPN-810 (molindone hydrochloride) was "very puzzling" to the Rockville, Md.-based firm, which will be "digging very deep into the data" with hopes of figuring out what went wrong. Shares (NASDAQ:SUPN) closed Wednesday at $19.93, down $9.20, or 31.6%. 
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Sulfide stress as new target?

Schizophrenia biomarker can be detected in human hair

Nov. 4, 2019
By John Fox
A subtype of schizophrenia is related to abnormally high brain levels of hydrogen sulfide (H2S), which has important implications for the development of new treatments, according to a study by researchers at the RIKEN Center for Brain Science (CBS) in Japan.
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Small and selective

Small molecules clear mutant Huntingtin protein

Oct. 31, 2019
By John Fox
A Chinese study has identified small-molecule compounds that can selectively reduce levels of the mutant Huntingtin (HTT) protein involved in the pathogenesis of Huntington's disease (HD), and possibly other neurodegenerative diseases involving mutant protein accumulation.
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Hardly DRP in the bucket, Nuplazid's new indication rates Acadia blockbuster?

Sep. 10, 2019
By Randy Osborne
Good news from San Diego-based Acadia Pharmaceuticals Inc.'s phase III trial with Nuplazid (pimavanserin) in dementia-related psychosis (DRP) had analysts trotting out music metaphors in reports about the study called Harmony, while talking already about would-be sales of the drug, a selective serotonin inverse agonist and antagonist that preferentially targets the 5-HT2A receptor.
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Neurotrope shares crushed on phase II bryostatin-1 fizzle in Alzheimer's

Sep. 10, 2019
By Michael Fitzhugh
Shares of New York-based Neurotrope Inc. (NASDAQ:NTRP) fell 77.3% to close at a record low of $1 Monday after a phase II study of its lead candidate, bryostatin-1, failed to outperform a placebo in helping people with moderate to severe Alzheimer's disease (AD) achieve improvement on a standardized measure of cognition.
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Pharnext shares drop 40% as FDA requests second pivotal trial in CMT

Sep. 3, 2019
By Cormac Sheridan
DUBLIN – Shares in Pharnext SA plunged by more than 40% Friday on news that the FDA requires the company to undertake a second phase III trial of its Charcot-Marie-Tooth disease type 1A (CMT1A) therapy PXT-3003.
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Not Accordion to plan, try in PD delivers Intec fizzle; phase III dosing too low?

July 23, 2019
By Randy Osborne
Given how many patients who completed the double-blind portion of the study opted into the extension segment and the quality of pharmacokinetic (PK) data, phase III testing of Intec Pharma Ltd.'s Accordion Pill (AP, carbidopa/levodopa [CD/LD]) against immediate-release CD/LD in Parkinson's disease (PD) seemed likely to ring the statistical significance bell.
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