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BioWorld - Tuesday, July 7, 2026
Home » Authors » Lee Landenberger

Lee Landenberger

Articles

ARTICLES

At intersection of integrated technology, Arsenalbio raises $85M in a series A financing

Oct. 18, 2019
By Lee Landenberger
It was at the constantly changing intersection of data science that Arsenal Biosciences Inc.'s CEO, Ken Drazan, found himself as he helped bring the company to life and to its $85 million series A fundraising.
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A complementary deal: Alexion to acquire Achillion for $930M up front, plus CVRs

Oct. 17, 2019
By Lee Landenberger
With Alexion Pharmaceuticals Inc.'s acquisition of Achillion Pharmaceuticals Inc. for about $930 million up front, Alexion expands and diversifies its pipeline into familiar territory – treating complement-mediated diseases. Blue Bell, Pa.-based Achillion is developing oral, small-molecule factor D inhibitors for treating complement alternative pathway-mediated rare diseases, including paroxysmal nocturnal hemoglobinuria and C3 glomerulopathy.
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Relmada's positive phase II depression data lift stock's spirits

Oct. 16, 2019
By Lee Landenberger
Top-line data from Relmada Therapeutics Inc.'s phase II study of REL-1017 (dextromethadone) in patients with treatment-resistant depression caused the stock to more than double Tuesday, a great day on the market.
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Lilly's Reyvow gets FDA approval for treating migraine

Oct. 15, 2019
By Lee Landenberger
When Eli Lilly and Co. took over Colucid Pharmaceuticals Inc. for nearly $1 billion in early 2017, it brought then-migraine candidate Reyvow (lasmiditan) back to its founder and now to its FDA approval for the acute treatment of migraine, with or without aura, in adults. Its unusual mechanism puts it outside many other approved migraine treatments, which could hinder its market penetration.
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Kodiak begins phase II in macular degeneration

Oct. 14, 2019
By Lee Landenberger
The first patients have been treated in Kodiak Sciences Inc.'s phase II DAZZLE trial of anti-VEGF antibody biopolymer conjugate KSI-301 in patients with treatment-naïve wet age-related macular degeneration. At least 368 patients worldwide are expected to enroll in the study. The primary endpoint will be assessed at one year and each patient will be treated and followed for two years.
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Alexion and Stealth cut elamipretide deal

Oct. 11, 2019
By Lee Landenberger
Alexion Pharmaceuticals Inc. and Stealth Biotherapeutics Corp. reached a deal for an option to co-develop and commercialize elamipretide for mitochondrial diseases.
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Bluebird, Novo Nordisk to collaborate on genome editing project, starting with hemophilia

Oct. 10, 2019
By Lee Landenberger
Bluebird Bio Inc. and Novo Nordisk A/S plan to develop in vivo genome editing treatments for genetic diseases, including hemophilia, over the next three years.
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Minoryx completes MIN-102 phase II recruitment early

Oct. 9, 2019
By Lee Landenberger
Minoryx Therapeutics SL, of Barcelona, completed recruitment early for its FRAMES phase II trial of MIN-102 (leriglitazone), a peroxisome proliferator-activated receptor gamma agonist, to treat Friedreich's ataxia.
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Akcea and Pfizer sign $250M up-front deal

Oct. 8, 2019
By Lee Landenberger
Akcea Therapeutics Inc., a majority owned affiliate of Ionis Pharmaceuticals Inc., and Pfizer Inc. signed an exclusive, worldwide licensing deal for AKCEA-ANGPTL-3-LRx, which is being developed to treat cardiovascular and metabolic diseases. The deal follows a period during which Akcea's stock (NASDAQ:AKCA) has sagged prior to rising Monday and big changes in the company's C-suite.
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Arbutus halts hep B study after volunteers develop hepatitis

Oct. 7, 2019
By Lee Landenberger
Rough times continued Friday at Arbutus Biopharma Corp. as it discontinued clinical development of AB-506, an oral capsid inhibitor, which is in a clinical trial for treating chronic hepatitis B. The decision was made when two healthy volunteers were found to have acute hepatitis.
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