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BioWorld - Tuesday, April 14, 2026
Home » Authors » Brian Orelli

Articles by Brian Orelli

Cystic fibrosis firms highlight precision medicine's potential

March 30, 2015
By Brian Orelli
With different mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) causing different severities of the disease and requiring different drugs to increase protein function, cystic fibrosis (CF) is the poster child of precision medicine.
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The other March Madness: Data from ACC (the heart one)

March 23, 2015
By Brian Orelli
Like the basketball Atlantic Coast Conference, the other ACC, the American College of Cardiology, ramps up this time of year with its annual scientific session.
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New spin on thin: CVOT and orphan data, ANDAs filed

March 16, 2015
By Brian Orelli
In drug development, it can be difficult to follow the crowd. And that goes double for a market like obesity that's struggled to gain traction.
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Hot capital markets push pharma to early stage deals

March 2, 2015
By Brian Orelli
SAN DIEGO – The capital flowing in the public markets makes it easier for biotechs to gain funding through IPOs and secondary offerings. Companies raised $6.5 billion through IPOs last year and more established public companies were able to add nearly $16.7 billion to their coffers according to BioWorld Snapshots.
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Hepatitis C market in flux: new data, discounts & lost BTDs

Feb. 17, 2015
By Brian Orelli
The hepatitis C market seems to do things in pairs.
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Biotechs welcome spotlight on precision medicine

Feb. 9, 2015
By Brian Orelli
As part of his proposed budget, President Barack Obama recommended spending $215 million on a Precision Medicine Initiative. (See BioWorld Today, Feb. 2, 2015.)
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Obesity market gets more players; improving, but challenges remain

Feb. 2, 2015
By Brian Orelli
The approval of Takeda Pharmaceuticals U.S.A.'s and Orexigen Therapeutics Inc.'s Contrave (naltrexone and bupropion) in September and Saxenda (liraglutide) from Novo Nordisk A/S last month doubled the number of obesity drugs approved by the FDA in the last two and a half years.
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Melanoma just the beginning for PD-1 pathway drugs

Jan. 20, 2015
By Brian Orelli
Both Merck & Co. Inc.’s Keytruda (pembrolizumab) and Bristol-Myers Squibb Co.’s Opdivo (nivolumab) were approved by the FDA to treat advanced metastatic melanoma last year, but that’s only the start of the possibilities for the PD-1 pathway drugs. (See BioWorld Today, Sept. 5, 2014.)
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VCs give the gift of capital; 2014 was a banner year for start-ups

Jan. 5, 2015
By Brian Orelli
Merry Christmas, happy Hanukkah, joyous Kwanzaa. Whatever you celebrated, the venture capitalists gave the biopharma industry a mighty large gift in 2014. Investments in private drug companies tracked by BioWorld Snapshots rounded out the year at $3.85 billion, up substantially from the $2.6 billion in 2013 in the U.S.
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Long-acting growth hormones prick their way to the market

Dec. 22, 2014
By Brian Orelli
Human growth hormone (hGH) is a $3.5 billion industry, but it's plagued by a major issue: All of the current versions of hGH (somatropin) – Novo Nordisk's Norditropin, Eli Lilly and Co.'s Humatrope, Roche AG unit Genentech Inc.'s Nutropin-AQ, Merck Serono's Saizen, Teva Pharmaceutical Industries Ltd.'s Tev-tropin, LG Life Science Ltd.'s Valtropin and Omnitrope, sold by Novartis AG's generic group Sandoz – have to be injected daily.
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