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Home » Authors » Lee Landenberger

Articles by Lee Landenberger

For $6.5B in cash, Johnson & Johnson will acquire Momenta

Aug. 19, 2020
By Lee Landenberger

Poseida phase I on clinical hold following a patient’s death

Aug. 18, 2020
By Lee Landenberger
Following a patient’s death in Poseida Therapeutics Inc.’s phase I trial of P-PSMA-101 in metastatic castrate-resistant prostate cancer (mCRPC), the FDA has put the study on clinical hold.
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Prinicipia Biopharma Inc.

In a $3.68B deal, Sanofi will acquire Principia

Aug. 17, 2020
By Lee Landenberger
Sanofi SA is acquiring Principia Biopharma Inc. in a $3.68 billion deal that brings Sanofi three clinical-stage BTK inhibitors and simplifies a partnership that began three years ago. Paris-based Sanofi plans to acquire all outstanding Principia common stock shares for $100 each at a $3.36 billion enterprise value. Sanofi will get SAR-442168 (PRN-2246), the brain-penetrant candidate at the heart of the deal. The agreement now gives Sanofi full control of the program, bringing a three-year partnership between the two companies to an end
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In a $3.68B deal, Sanofi will acquire Principia

Aug. 17, 2020
By Lee Landenberger

European Commission’s first COVID-19 deal goes to Astrazeneca while Novavax signs U.K agreement

Aug. 14, 2020
By Lee Landenberger
Astrazeneca plc is the first company to sign an agreement with the European Commission to supply a COVID-19 vaccine.
Read More
Microscope and coronavirus illustration

Moderna receives $1.525B in COVID-19 funding as costs per dose drop

Aug. 12, 2020
By Lee Landenberger
The U.S. government bought 100 million doses of mRNA-1273 from Moderna Inc., of Cambridge, Mass., with a new award worth up to $1.525 billion, a deal that drops the implied cost per dose below that of several other companies receiving funding through the government program.
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Boy in wheelchair, scenic overlook

Fulcrum looks for balance in its phase II FSHD study

Aug. 11, 2020
By Lee Landenberger
An interim analysis from Fulcrum Therapeutics Inc.’s phase II study of losmapimod for treating facioscapulohumeral muscular dystrophy (FSHD) produced data that pleased the CEO and displeased investors.
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FDA approved metal stamp

FDA approves Trevena’s Olinvyk for clinical controlled settings

Aug. 10, 2020
By Lee Landenberger
Knocked back by a complete response letter (CRL) in late 2018, Trevena Inc. dusted itself off, resubmitted its NDA for oliceridine and found satisfaction as the FDA has approved the opioid agonist.
Read More
Triatomine insect on target

Bayer’s Lampit approved by FDA for treating Chagas disease

Aug. 7, 2020
By Lee Landenberger
Bayer AG’s Lampit (nifurtimox) to treat Chagas disease in pediatric patients, approved by the FDA on Friday, is an oral, antiprotozoal medication for newborns to patients under 18, who weigh at least 2.5 kg and are diagnosed with Chagas disease caused by Trypanosoma cruzi.
Read More

Bayer’s Lampit approved by FDA to treat Chagas disease

Aug. 7, 2020
By Lee Landenberger
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