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BioWorld - Tuesday, January 20, 2026
Home » Authors » Michael Fitzhugh

Articles by Michael Fitzhugh

Exelixis enlists Aurigene in new cancer-focused discovery, development deal

Aug. 2, 2019
By Michael Fitzhugh
Fresh off a second quarter featuring what Exelixis Inc. CEO Michael Morrissey called "strong momentum" for its lead product, Cabometyx (cabozantinib), the California company has inked a multimillion-dollar oncology deal with Bangalore, India-based Aurigene Discovery Technologies Ltd., a small-molecule specialist owned by Dr. Reddy's Laboratories Ltd. 
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Janssen quits $730M partnership with Alligator in portfolio shuffle

Aug. 1, 2019
By Michael Fitzhugh
Sweden's Alligator Bioscience AB said Janssen Biotech Inc. has terminated its 2015 licensure of the Swedish company's CD40-directed antibody, ADC-1013, following a strategic portfolio decision to prioritize other assets. 
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Foamix secures $64M to support commercial prep for acne, rosacea candidates

July 31, 2019
By Michael Fitzhugh
Foamix Pharmaceuticals Ltd., an Israeli specialty pharma developing foam-based formulations of minocycline for moderate-to-severe acne and rosacea, has secured up to $64 million in financing from Perceptive Advisors and Orbimed, its two largest shareholders. The funds, comprised of loans and proceeds of a registered direct offering, are expected to support potential commercial launches for FMX-101 and FMX-103, pending FDA approval, the company said.
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Lexicon shares crash after Sanofi abandons diabetes alliance

July 30, 2019
By Michael Fitzhugh
Shares of Lexicon Pharmaceuticals Inc. (NASDAQ:LXRX) fell 70.3% Monday to $1.69 as Sanofi SA terminated a $1.7 billion diabetes collaboration with the company. The decision followed two trials in which Zynquista (sotagliflozin), a dual SGLT inhibitor, failed to make a statistically significant dent in blood sugar control in patients with chronic kidney disease, a common result of diabetes.
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FDA puts partial clinical hold on Regulus kidney disease trial

July 25, 2019
By Michael Fitzhugh
Following more than a year of restructuring and recalibration, Regulus Therapeutics Inc. is facing a new partial clinical hold placed by the FDA on its phase I test of RGLS-4326, an oligonucleotide it's developing for the treatment of autosomal dominant polycystic kidney disease (ADPKD). 
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Biogen profits buoyed by MS franchise, but sales of Spinraza for SMA miss mark

July 24, 2019
By Michael Fitzhugh
Growing sales of its multiple sclerosis (MS) therapies and lower R&D expenses led Biogen Inc. to beat both top- and bottom-line expectations during the second quarter, despite lower-than-expected sales of its spinal muscular atrophy (SMA) drug, Spinraza (nusinersen).
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Bioxcel sees support for pivotal trial in phase Ib agitation study

July 23, 2019
By Michael Fitzhugh
Drug "re-innovation" specialist Bioxcel Therapeutics Inc. is gearing up to discuss a pivotal phase III trial for BXCL-501 with the FDA after top-line results of a phase Ib study showed it reduced schizophrenia-associated agitation while calming trial participants without excessive sedation. H.C. Wainwright & Co. analyst Raghuram Selvaraju called the results "highly favorable" and suggested the drug, a sublingual-formulated version of dexmedetomidine, could reach market as soon as 2021.
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Phagomed closes €2.3M seed round to back phage therapy development

July 16, 2019
By Michael Fitzhugh

Phagomed closes €2.3M seed round to back phage therapy development

July 12, 2019
By Michael Fitzhugh
Phagomed Biopharma GmbH, a Viennese company born of frustrations with the rise of multidrug-resistant infections and confidence in the potential for bacteriophage therapies to address them, has landed a €1.5 million (US$1.7 million) equity investment from new and existing investors. It's the second part of a €2.3 million seed financing, raised ahead of a series A round the company hopes to secure in 2020 to help it move toward the clinic in 2021.
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Revolution raises $100M series C to tackle RAS-dependent cancers

July 10, 2019
By Michael Fitzhugh
Revolution Medicines Inc., a California-based company developing a small-molecule inhibitor of SHP2 in partnership with Sanofi SA and other programs targeting mutant forms of the key signaling protein RAS, has raised a $100 million series C equity financing led by Boxer Capital LLC, an investment firm funded by British businessman Joe Lewis' Tavistock Group, which has backed financings of companies including G1 Therapeutics Inc., Kura Oncology Inc. and, more recently, Encoded Therapeutics Inc.
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