The latest news from the global pharmaceutical industry. Below you will find news and information to keep you up-to-date with what is happening in your industry. Coverage includes regulatory approvals, recall announcements, mergers and acquisitions, personnel news and appointments, new facility and facility expansion updates, collaborations and agreements, and financial updates.
Moderna announced that the U.S. government has secured 100 million doses of mRNA-1273.
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The FDA notified IGC it has authorized the initiation Phase 1 human trial study for the Company’s investigational cannabinoid formulation for the ...
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Kineta announced the CTA approval in the Netherlands for initiation of a first in-human clinical trial of KCP506.
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Kaiser Permanente has begun participating in a phase 3 clinical trial to test an investigational vaccine against SARS-CoV-2, the virus causing the ...
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Hoth Therapeutics has submitted for ethics approval in Australia for its planned Clinical study of its therapeutic BioLexa for Atopic Dermatitis.
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Verrica has entered into an exclusive worldwide license agreement with Lytix Biopharma AS to develop and commercialize LTX-315 for dermatologic ...
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Romark announced the initiation of a Phase 3 clinical trial of its investigational new drug candidate NT-300 as a treatment for mild or moderate COVID...
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Regeneron announced the FDA has accepted for Priority Review a BLA for evinacumab as an adjunct to other lipid-lowering therapies in patients with ...
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Boehringer Ingelheim announced the first patient has enrolled in a trial assessing nintedanib in children and adolescents with fibrosing interstitial ...
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Vaccibody and Nektar announced the first patient has been dosed in the study evaluating bempegaldesleukin with VB10.NEO.
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Thursday, August 13, 2020
The FDA approved Olinvyk, an opioid agonist for moderate to severe acute pain in adults, where the pain is severe enough to require an intravenous ...
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Thursday, August 13, 2020
Seelos received notice from the FDA that the company may proceed with initiating a trial studying SLS-005 for the treatment of ALS.
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Thursday, August 13, 2020
Clearside Biomedical announced the FDA has accepted its IND application for CLS-AX, for CLS-AX in wet AMD patients by the end of 2020.
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Thursday, August 13, 2020
Protalix BioTherapeutics together with Chiesi Global Rare Diseases announced the FDA has accepted the BLA and granted Priority Review designation for ...
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Wednesday, August 12, 2020
PTC announced the FDA has approved Evrysdi for spinal muscular atrophy in adults and children 2 months and older.
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