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BioWorld - Monday, December 22, 2025
Home » Authors » Brian Orelli

Brian Orelli

Articles

ARTICLES

Biocom panel
Biocom Global Life Sciences Partnering Conference

Pharmas share their needs, wants and offer some advice

March 2, 2020
By Brian Orelli
SAN DIEGO – At the Biocom 10th Annual Global Life Sciences Partnering Conference, panels of pharma executives highlighted what they're looking for to supplement their pipelines and offered advice that ran the gamut from company formation to the courting process to strategies for partnering pipeline drugs and platforms.
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John Hood at the Biocom Global Life Sciences
Sometimes it takes an advocate (or four)

Backstory of the FDA lifting its clinical hold and eventual approval of Inrebic

Feb. 28, 2020
By Brian Orelli
SAN DIEGO – At Biocom's 10th Annual Global Life Sciences Partnering Conference, a panel of players intimately familiar with last year's approval of myelofibrosis treatment Inrebic (fedratinib) explained the backstory of how they got the JAK2 kinase inhibitor off an FDA clinical hold, wrangled the rights to the drug back from the big pharma owner that had acquired the drug from Targegen Inc. and eventually helped the drug gain FDA approval after selling the rights to another large company.
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Serving piece of pie chart
Multiple spin-offs in the works

Pharmas break up to accelerate growth

Feb. 11, 2020
By Brian Orelli
Even as the volume of mergers and acquisitions in 2019 reached the highest level in the last 10 years, multiple big pharma companies are looking to get smaller, spinning off units into separate entities.
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Inflammatory/Immune: Filgotinib

Filgotinib looks to JAK up sales with multiple indications

Feb. 10, 2020
By Brian Orelli
Filgotinib (GLPG-0634) has the potential to be a blockbuster drug, according to Cortellis Drugs to Watch analysis, but it may take a few approvals in various indications to reach the coveted mark of $1 billion in annual sales.
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DNA illustration

Gene therapies could add $45B to health care costs over next five years

Jan. 27, 2020
By Brian Orelli
New gene therapy treatments could add $45 billion to the cost of health care over the next five years, according to a new report from CVS Health Corp., of Woonsocket, R.I. While the number is staggering, without knowing the price of the currently unapproved therapies, how many patients will seek treatment and the likelihood of approval, the pharmacy benefit manager's estimate is basically an educated guess.
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'Holy grail'

Adaptimmune SPEARs 4 partial responses in various tumor types

Jan. 13, 2020
By Brian Orelli
While companies have seen plenty of success treating blood cancers with T-cell therapies, solid tumors have largely remained the holy grail for T cells. But Adaptimmune Therapeutics plc has early data from its Specific Peptide Enhanced Affinity Receptor T-cell platform suggesting it may be on the right path for a platform with a wide breadth.
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Let them eat steak

Ultragenyx flying high on responders to its gene therapy for ornithine transcarbamylase deficiency

Jan. 10, 2020
By Brian Orelli
The prospects for Ultragenyx Pharmaceutical Inc.'s adeno-associated virus (AAV) gene therapy, DTX-301, in patients with ornithine transcarbamylase (OTC) deficiency weren't looking too great after treatment of the first two cohorts in a phase I/II study.
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The biotech industry remembers: In Memoriam

Jan. 10, 2020
By Brian Orelli
As the industry looks forward to 2020 at the 38th Annual J.P. Morgan Healthcare Conference next week, BioWorld is looking backward to those we lost in the past year.
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Head filled with digital data
'The new gold rush'

AI, machine learning offer hope for speeding Alzheimer’s development

Dec. 16, 2019
By Brian Orelli
Machine learning and artificial intelligence (AI) are already being actively used in drug discovery to evaluate potential binding of small-molecule drugs to proteins, but there's potential for the technologies to be used on the development side as well, especially in hard-to-treat diseases such as Alzheimer's disease.
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CTAD 2019

Small Alzheimer’s drug companies look to advance quickly into late-stage

Dec. 9, 2019
By Brian Orelli
SAN DIEGO – Smaller companies looking to move their Alzheimer’s disease drugs into late-stage testing as quickly as possible are eschewing cognitive endpoints that can take years to readout for biomarkers and functional assays of brain activity.
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View All Articles by Brian Orelli

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