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BioWorld - Friday, December 26, 2025
Home » Authors » Brian Orelli

Articles by Brian Orelli

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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FDA sign
From FDAAA to the Cures Act

FDA shifts gears on real-world evidence

Nov. 18, 2019
By Brian Orelli
The FDA has typically used real-world evidence (RWE) as a way of monitoring safety issues post-approval, especially through the Sentinel Initiative, which started in response to the FDA Amendments Act of 2007.
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Roche and PTC check off another SMA win, but the devil is in the details

Nov. 12, 2019
By Brian Orelli
Roche Holding AG and PTC Therapeutics Inc. together with their partner, the SMA Foundation, reported success in part two of the pivotal Sunfish study testing their survival motor neuron-2 splicing modifier risdiplam in patients with type 2 or 3 spinal muscular atrophy (SMA).
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Test tube, dropper

From open science to a helping hand, companies, researchers collaborate

Nov. 4, 2019
By Brian Orelli
Companies and academic researchers have often had a dichotomous relationship, but new models are aligning the relationship.
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Gene therapy offers potential but poses logistical challenges

Oct. 14, 2019
By Brian Orelli
The mantra for a while has been that it's not good enough to get your drug approved, you've got to get it payed for, too. For gene therapy treatments, the payment is more complex, and you can add manufacturing and supply chain logistics to the list of challenges.
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Three late-stage drugs look to battle in Cushing's syndrome market

Oct. 2, 2019
By Brian Orelli
The Cushing's syndrome market is heating up with three second-generation drugs in late-stage development to join the two approved medications, Signifor (pasireotide, Recordati SpA) and Korlym (mifepristone, Corcept Therapeutics Inc.), as well as a couple of off-label options.
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Three late-stage drugs look to battle in Cushing's syndrome market

Sep. 30, 2019
By Brian Orelli
The Cushing's syndrome market is heating up with three second-generation drugs in late-stage development to join the two approved medications, Signifor (pasireotide, Recordati SpA) and Korlym (mifepristone, Corcept Therapeutics Inc.), as well as a couple of off-label options.
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Artificial intelligence helps little drug developers compete

Sep. 18, 2019
By Brian Orelli
After doing deals with big pharma – Eli Lilly and Co., Merck & Co. Inc., Abbvie Inc. and Bayer AG – Atomwise Inc. announced three partnerships last week with smaller preclinical companies to use its artificial intelligence (AI) platform to develop drugs for their targets.
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Artificial intelligence helps little drug developers compete

Sep. 16, 2019
By Brian Orelli
After doing deals with big pharma — Eli Lilly and Co., Merck & Co. Inc., Abbvie Inc. and Bayer AG — Atomwise Inc. announced three partnerships last week with smaller preclinical companies to use its artificial intelligence (AI) platform to develop drugs for their targets.
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