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BioWorld - Tuesday, February 17, 2026
Home » Authors » Marie Powers

Marie Powers

Articles

ARTICLES

Pfizer’s Refocus May Bring Clarity for Lpath

Oct. 10, 2013
By Marie Powers
Lpath Inc. moved quickly to digest the disappointment that partner Pfizer Inc. plans to divest “a number of” its ophthalmology R&D assets, including its exclusive option for a global license to develop and commercialize Lpath’s wet age-related macular degeneration (AMD) candidate Isonep. Scott Pancoast, Lpath’s president and CEO, said the path forward for Isonep is a choice between regaining rights to the compound, currently in a four-arm Phase II study, or having them reassigned to a third-party bidder – either of which offers potential upside.
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Pharmas Add $42M in Merus’ Series B Extension Round

Oct. 9, 2013
By Marie Powers
Merus BV enticed Johnson & Johnson Development Corp. (JJDC) to join existing investors Novartis Venture Fund and Pfizer Venture Investments for a big pharma trifecta in a €31 million (US$42 million) extension to its Series B financing.
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Eleison Seeks Phase III Success with Glufosfamide

Oct. 9, 2013
By Marie Powers
Eleison Pharmaceuticals LLC moved lead compound glufosfamide into a Phase III study in second-line pancreatic cancer, seeking to achieve success in a drug that was a near-miss in previous hands. The pivotal study is assessing whether glufosfamide improves survival compared to bolus 5-FU in patients with metastatic pancreatic cancer who progressed or failed therapy on a gemcitabine-based regimen.
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‘SINE’ and Dandy: Karyopharm Seeks $80M IPO

Oct. 8, 2013
By Marie Powers
The initial public offering (IPO) palooza continued into October with two more filings, including one by Karyopharm Therapeutics Inc. seeking to raise up to $80 million. Karyopharm’s S-1 was filed just two months after the biotech closed a $19 million Series B extension that propelled its venture financing to $97.2 million.
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Ligand Scores on FDA Approval of Pfizer’s Hot Flash Drug Duavee

Oct. 7, 2013
By Marie Powers
Ligand Pharmaceuticals Inc. scored the first direct hit from its decades-long collaboration with Pfizer Inc. as the FDA approved Duavee (conjugated estrogens/bazedoxifene) in a once-daily 0.45-mg/20-mg tablet form. The drug, formerly known as Aprela, is indicated for moderate to severe vasomotor symptoms – commonly known as hot flashes – associated with menopause and for the prevention of postmenopausal osteoporosis.
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Pharmas Add $42M in Merus Series B Extension

Oct. 4, 2013
By Marie Powers
Merus BV enticed Johnson & Johnson Development Corp. (JJDC) to join existing investors Novartis Venture Fund and Pfizer Venture Investments for a big pharma trifecta in a €31 million (US$42 million) extension to its Series B financing.
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Surf’s Up: Investor Interest Swells $377M Frazier Fund

Oct. 3, 2013
By Marie Powers
Capitalizing on the rising tide of investor enthusiasm for biopharma, investment firm Frazier Healthcare closed its seventh venture fund, surpassing its $300 million target by more than 25 percent with commitments of $377 million.
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Abbvie and Galapagos Cozy Up in Second Deal

Oct. 2, 2013
By Marie Powers
One day after disclosing an $840 million licensing deal with Ghent, Belgium-based Ablynx NV for nanobody technology to treat rheumatoid arthritis and systemic lupus erythematosus, Abbvie Inc. turned to another Belgian biotech – existing partner Galapagos NV – for a global alliance to discover, develop and commercialize potentiator and combination therapies in cystic fibrosis (CF).
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Merck Brings Down Hammer on R&D, Cuts 8,500 More Jobs

Oct. 2, 2013
By Marie Powers
In a move Merck & Co. Inc. chairman and CEO Kenneth C. Frazier took pains to explain as “creating greater efficiencies,” the pharma giant acceded to calls from analysts and investors to remake its R&D operation, disclosing the elimination of another 8,500 positions, in addition to previously reported reductions of 7,500 jobs, with a goal of paring annual operating expenses by approximately $2.5 billion by the end of 2015.
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Lion Roars on Long-Term Metastatic Melanoma Data

Oct. 1, 2013
By Marie Powers
Little Lion Biotechnologies Inc., the surviving entity of a merger earlier this year with Genesis Biopharma Inc., reported promising long-term findings from a Phase II trial in Stage IV metastatic melanoma. The study was conducted by the National Cancer Institute (NCI) using tumor-infiltrating lymphocyte (TIL) technology licensed by the company and in development under a five-year Cooperative Research and Development Agreement that Genesis inked with the Institute in 2011.
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