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BioWorld - Friday, January 2, 2026
Home » Authors » Brian Orelli

Articles by Brian Orelli

An alarming rate of cancer clinical trials ending early

Feb. 3, 2014
By Brian Orelli
Last week, Cambridge, Mass.-based Aveo Oncology and Astellas Pharma Inc., of Tokyo, announced that they were discontinuing a Phase II trial testing tivozanib in patients with locally recurrent or metastatic triple negative breast cancer due to insufficient enrollment.
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Social media: Broadcast trumps engagement for now

Jan. 27, 2014
By Brian Orelli
Nearly half of pharmaceutical companies can be found on social media websites according to a report by IMS Institute for Healthcare Informatics, but most use their accounts as a broadcasting channel with very little interaction with patients and doctors.
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Reverse splits couldn’t hold these companies down

Jan. 13, 2014
By Brian Orelli
Reverse splits have a bad reputation amongst investors, causing biotechs, for the most part, to avoid them at all cost.
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Have RNA therapeutics lived up to their lofty expectations?

Jan. 6, 2014
By Brian Orelli
Last January, BioWorld Insight asked whether, after a long bumpy road, RNA therapeutics could prosper in 2013. With a few exceptions, the answer was a resounding yes. (See BioWorld Insight, Jan. 7, 2013.)
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Series A investments boost 2013 for VC-backed biopharmas

Jan. 6, 2014
By Brian Orelli
U.S. biopharmaceutical companies capped 2013 with the strongest quarter of the year, raising $835 million in 37 venture capital deals in the fourth quarter according to data compiled by BioWorld Snapshots.
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Drug compounders registering to satisfy terms of new law

Dec. 17, 2013
By Brian Orelli

The Compounding Quality Act, part of the Drug Quality and Security Act, signed into law last month, creates a volunteer registration of “outsourcing facilities” that will be subject to scrutiny by the FDA, including routine inspections.


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Forest joins restructuring mania, focus on streamlining

Dec. 9, 2013
By Brian Orelli
Forest Laboratories Inc. joined the litany of big pharma companies announcing restructuring programs last week. But the major restructuring, dubbed Project Rejuvenate, appears to be more about streamlining operations than downsizing.
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Filings and Review Times Increase FDA Approvals

Dec. 2, 2013
By Brian Orelli
The FDA approved 35 new molecular/biological entities (NMEs/NBEs) on average in 2011-2012, substantially higher than the 20-year average of 28 approvals.
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Gene Therapy Expression: No Problem from Immune System

Nov. 25, 2013
By Brian Orelli
Adeno-associated virus (AAV)-based systems are ideally suited for delivering gene therapy. After the viral vector infects the cell, the DNA doesn’t integrate into the host genome, instead existing primarily in an episomal form, which allows for long-term expression in nonreplicating cells without DNA damage to the host cells and the risk of inducing malignancy.
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Curemark Moves Toward Approval of First Autism Drug

Nov. 18, 2013
By Brian Orelli
While some genes have been linked to autism spectrum disorder, the exact cause of the disease isn’t known. With a dearth of knowledge about the disease, there haven’t been any drugs specifically developed to treat autism, although Risperdal (risperidone, Johnson & Johnson) and Abilify (aripiprazole, Bristol-Myers Squibb Co. and Otsuka Pharmaceutical Co. Ltd) are approved to treat irritability associated with autism.
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