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BioWorld - Saturday, January 31, 2026
Home » Authors » Michael Fitzhugh

Articles by Michael Fitzhugh

Celgene, Agios Pharmaceuticals win FDA approval for IDH2-targeting Idhifa in AML

Aug. 2, 2017
By Michael Fitzhugh
A new therapy for certain adults with relapsed or refractory acute myeloid leukemia (AML), developed by Celgene Corp. and Agios Pharmaceuticals Inc., has won earlier-than-expected FDA approval following a priority review.
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Mateon candidate shows ongoing signs of activity against AML, MDS in early trial

Aug. 1, 2017
By Michael Fitzhugh
Mateon Therapeutics Inc. said that, so far, five of 21 people with relapsed/refractory acute myeloid leukemia (AML) or myelodysplastic syndrome have achieved complete remissions after being treated with its vascular disrupting agent, Oxi-4503, in combination with cytarabine during a phase Ib dose-escalation study.
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Nantcell bets up to $365M on Cytrx's aldoxorubicin

July 31, 2017
By Michael Fitzhugh
Nantcell Inc., the Patrick Soon-Shiong-backed company built in part with funds from the blockbuster albumin-bound chemotherapy Abraxane (nab-paclitaxel), has exclusively licensed Cytrx Corp.'s aldoxorubicin, another albumin-bound therapy, to incorporate into the treatment of multiple tumor types in combination with other immuno-oncology and cell-based therapies.
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Alexion axes R&D partnerships amid day of mixed Q2 news for biopharma earnings

July 28, 2017
By Michael Fitzhugh
An Alexion Pharmaceuticals Inc. decision to cut ties with Moderna Therapeutics Inc., Blueprint Medicines Corp. and Arbutus Biopharma Corp. led an eventful day of biopharma earnings reports, shaped by better-than-expected results at the rare disease specialist.
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Biogen sails to strong 2nd quarter on winds of SMA drug sales

July 26, 2017
By Michael Fitzhugh
Strong sales of Biogen Inc.'s pricey spinal muscular atrophy drug, Spinraza (nusinersen), helped the company cruise past consensus estimates and hit record second-quarter sales on Tuesday.
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Mitsubishi Tanabe to buy Neuroderm for $1.1 billion

July 25, 2017
By Michael Fitzhugh

Mitsubishi Tanabe Pharma Corp. is buying Israel-based Neuroderm Ltd., the developer of a belt-worn pump for the continuous delivery of liquid levodopa/carbidopa to treat severe Parkinson’s disease (PD), for $1.1 billion in cash, or $39 per share. The deal is expected to play a key role in helping the Japanese company reach its goal of earning ¥80 billion (US$719.5 million) in U.S. revenue by 2020, in part by expanding its U.S. neurology portfolio.


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Mitsubishi Tanabe to buy PD pump developer Neuroderm for $1.1B

July 25, 2017
By Michael Fitzhugh
Mitsubishi Tanabe Pharma Corp. is buying Israel-based Neuroderm Ltd., the developer of a belt-worn pump for the continuous delivery of liquid levodopa/carbidopa to treat severe Parkinson's disease (PD), for $1.1 billion in cash, or $39 per share. The deal is expected to play a key role in helping the Japanese company reach its goal of earning ¥80 billion (US$719.5 million) in U.S. revenue by 2020, in part by expanding its U.S. neurology portfolio.
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Mitsubishi Tanabe to buy Neuroderm for $1.1 billion

July 25, 2017
By Michael Fitzhugh
Mitsubishi Tanabe Pharma Corp. is buying Israel-based Neuroderm Ltd., the developer of a belt-worn pump for the continuous delivery of liquid levodopa/carbidopa to treat severe Parkinson's disease (PD), for $1.1 billion in cash, or $39 per share.
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Trevi raises $50.5 million series C, led by NEA

July 21, 2017
By Michael Fitzhugh
Trevi Therapeutics Inc. said a new $50.5 million series C financing led by New Enterprise Associates will help it advance the development of Nalbuphine ER, a twice-daily oral opioid in development for the treatment of two forms of severe itching. The round included new investors Lundbeckfonden Ventures, Omega Funds and Aperture Venture Partners, along with TPG Biotech, Trevi's largest investor and the leader of its $12.8 million series A in December 2012 and $25 million series B round in June 2014.
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Academics, payers suggest closing loopholes as FDA considers how to improve generics market

July 19, 2017
By Michael Fitzhugh
FDA staffers gathered to hear advice on better balancing support for new drug development with efforts to speed access to lower-cost generics got an earful from generics companies, payers and their representatives about how loopholes, citizen petitions and market gaming have left the balance of power tilted toward innovators.
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