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BioWorld - Saturday, June 20, 2026
Home » Authors » Randy Osborne

Randy Osborne

Articles

ARTICLES

Cascade crusade: Apellis taking delivery of $47M in C3 'p.o.' box for trials

Feb. 16, 2016
By Randy Osborne
Apellis Pharmaceuticals Inc.'s $47.1 million in series D money will let the company reach "some inflection points in rare diseases and geographic atrophy [GA] in the next year or so," general counsel David Watson told BioWorld Today, though he declined to provide specifics. "We're going to leave that open for now," he said.
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Incyte spurns Jakafi solid tumors, says 'IDO' to broad phase II combo program in cancer

Feb. 12, 2016
By Randy Osborne

Incyte Corp.'s decision to back away from experiments in solid tumors with Janus kinase 1 (JAK1)/JAK2 inhibitor Jakafi (ruxolitinib) was not exactly a surprise but undercuts future profit potential for the drug – still selling well in its approved indications – and turned investor attention to the indoleamine 2, 3-dioxygenase (IDO) program with epacadostat, bound for phase III trials in melanoma this year.


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Mylan takes over Meda in $9.9B cash, stock deal

Feb. 11, 2016
By Randy Osborne

Generics specialist Mylan N.V. said it would buy Sweden's Meda AB for about SEK83.6 billion (US$9.9 billion), including debt, in a combination of cash and stock.


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Weight and see: Phase III with Alkermes' duo tablet superior in schizophrenia?

Feb. 11, 2016
By Randy Osborne
Alkermes plc's phase III program with the antipsychotic ALKS 3831 for schizophrenia is designed to find out whether the tablet – which combines olanzapine with the firm's opioid antagonist samidorphan – can get around the weight-gain and metabolic problems that come with olanzapine by itself.
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Bellerophon drug-device wins big in phase II data; SPA covers ongoing effort

Feb. 10, 2016
By Randy Osborne

Bellerophon drug-device wins big in phase II data; SPA covers ongoing effort

Feb. 10, 2016
By Randy Osborne
CEO Jonathan Peacock told BioWorld Today that the phase III program with drug-device combo Inopulse in pulmonary arterial hypertension (PAH) will start "hopefully in the next few weeks," now that Bellerophon Therapeutics Inc. has in hand a positive analysis of final phase II data with the inhaled nitric-oxide product.
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Whose kallikrein now? Biocryst phase IIb slip in HAE shows oral therapy not a 'Shire' thing

Feb. 9, 2016
By Randy Osborne

Less than a month after Shire plc finished its $5.9 billion buyout of kallikrein player Dyax Corp., Biocryst Pharmaceuticals Inc.'s unhappy phase IIb data with an oral, liquid-filled soft-gel candidate avoralstat in the same class for hereditary angioedema (HAE) hobbled the firm on Wall Street and turned investor hopes toward the same drug's solid form, which has shown better, dose-dependent exposure for longer in preclinical models, along with a next-generation prospect.


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TROP-2 it: Moving quickly toward pivotal phase III, Immunomedics vs. TNBC

Feb. 8, 2016
By Randy Osborne
Looking ahead to the pivotal trial in triple-negative breast cancer (TNBC) with IMMU-132, slated to begin this summer, Immunomedics Inc. stands as "the only game in town at the moment this far along that has an antibody that targets this [TROP-2] receptor," Chau Cheng, director of investor relations, told BioWorld Today.
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Patchwork tilt? Corium's Aricept PK data hinting skin win after Japan fail

Feb. 5, 2016
By Randy Osborne
With a possible fix for compliance and side-effect issues in Alzheimer's disease (AD), Corium International Inc. drew attention from Wall Street by way of positive top-line phase I data that disclosed pharmacokinetics (PK) of its Corplex once-weekly transdermal patch delivering the acetylcholinesterase inhibitor donepezil, sold as oral, daily Aricept by Pfizer Inc.
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Line item: Heat Biologics expecting to handle glitch without delay of phase II

Feb. 4, 2016
By Randy Osborne
The misidentified cell line on which Heat Biologics Inc. based its cancer therapy HS-410 (vesigenurtacel-L) represents "a labeling problem that occurred very early in development," chief scientific officer Taylor Schreiber told BioWorld Today, and the paperwork matter should be resolved quickly with the FDA.
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