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BioWorld - Monday, February 16, 2026
Home » Authors » Randy Osborne

Randy Osborne

Articles

ARTICLES

Shuffling the Dex: Ocular, Eyepoint playing in space where none holds all aces

Dec. 4, 2018
By Randy Osborne
Ocular Therapeutix Inc. said the therapeutic area has plenty of room for its newly approved Dextenza (dexamethasone ophthalmic insert) 0.4 mg for postoperative eye pain along with Eyepoint Pharmaceuticals Inc.'s single-dose, sustained-release, intracameral Dexycu (dexamethasone intraocular suspension) 9 percent, granted U.S. marketing clearance earlier this year for inflammation after surgery.
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High noon in MG nearing, Ra may shine in phase II; C5 road paved by Soliris?

Dec. 3, 2018
By Randy Osborne
With dosing complete in its phase II trial testing Ra Pharmaceuticals Inc.'s RA-101495 in generalized myasthenia gravis (MG) and date likely to roll out near the end of this year, the world already has begun weighing odds of the compound in a space where the likes of Alexion Pharmaceuticals Inc. and Argenx SE are formidable players.
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High noon in MG nearing, Ra may shine in phase II; C5 road paved by Soliris?

Dec. 3, 2018
By Randy Osborne
With dosing complete in its phase II trial testing Ra Pharmaceuticals Inc.'s RA-101495 in generalized myasthenia gravis (MG) and date likely to roll out near the end of this year, the world already has begun weighing odds of the compound in a space where the likes of Alexion Pharmaceuticals Inc. and Argenx SE are formidable players.
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Weight for it: Alkermes bid nails endpoints but Street schizophrenia bar higher?

Nov. 30, 2018
By Randy Osborne
Full results are not due until the spring, but investors meanwhile didn't seem much enthused by Dublin-based Alkermes plc's positive top-line results from Enlighten-2, a pivotal phase III study of ALKS-3831 (olanzapine/samidorphan), a once-daily, oral atypical antipsychotic prospect for schizophrenia.
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Sifting hemophilia ASH's: Gene therapy tries to Spark hope, Biomarin out front

Nov. 29, 2018
By Randy Osborne
Cancer data typically steal the show at the American Society of Hematology (ASH) meeting, but hemophilia often gets plenty of play as well, and this time around could be especially compelling for investors in firms with therapies in the works for the clotting disorder.
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Screen savior: Vitrakvi OK brings selection challenge, but Bayer paving the way

Nov. 28, 2018
By Randy Osborne
How to assure screening for patients in whom just-approved Vitrakvi (larotrectinib) most likely will help is something "we've been working very hard for the last nine months" to establish, Joseph Germino, vice president of medical affairs for oncology with Bayer AG, told BioWorld. "The drug is so effective – it doesn't work in everybody [but] it works in most people – that it would be a shame if somebody were not able to get it because nobody checked" for eligibility.
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Back from the Edge post aSAH fizzle, PDS merger makes for renewal in I-O

Nov. 27, 2018
By Randy Osborne
Edge Therapeutics Inc.'s hunt for a "strategic alternative" after the failure of its flagship candidate, EG-1962 (nimodipine microparticles), ended with a stock-for-stock merger deal with privately held immuno-oncology (I-O) specialist Protein Delivery Sciences Biotechnology Corp. (PDS).
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Gorlin for the gold in skin, Leo pledges up to $760M; Pellepharm phase III near

Nov. 21, 2018
By Randy Osborne
With a "cosmetically elegant" topical therapy, Pellepharm Inc. CEO Sanuj Ravindran told BioWorld that his firm is hoping to exploit the upside of hedgehog inhibition demonstrated so well by Erivedge (vismodegib, Roche Holding AG) while avoiding the downside of a systemic therapy with that mechanism of action in basal cell carcinoma (BCC).
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The PAHs that refreshes: Arena collecting $800M, United franchise buoyed

Nov. 16, 2018
By Randy Osborne
Arena Pharmaceuticals Inc. CEO Amit Munshi said the $800 million up-front, worldwide licensing deal with United Therapeutics Corp. centered on prostacyclin (IP) receptor agonist ralinepag in pulmonary arterial hypertension (PAH) "allows us a broader push in the GI [gastrointestinal] space" with S1P receptor modulator etrasimod, which has reached the planning stage for phase III trials in ulcerative colitis (UC).
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Kymera gets $65M in series B as protein degradation nears clinic

Nov. 14, 2018
By Randy Osborne
Founder and Chief Technology Officer Nello Mainolfi told BioWorld that Kymera Therapeutics Inc. will disclose more in the months ahead about its lead compound, which sits at "the juncture between oncology and inflammation" and has been widely implicated in hematological cancers as well as other conditions. Meanwhile, the Cambridge, Mass.-based firm's $65 million series B round will push that prospect into the clinic and advance the pipeline of other candidates in cancer and immunology. So far, the Pegasus protein degradation platform has yielded preclinical data packages that support drug-like properties of Kymera's assets as well as differentiated pharmacology, Kymera said.
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