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Cannabics Plans pre-IND Meeting Request for Colon Cancer Drug Candidate americanpharmaceuticalreview
October 28, 2020
Cannabics Pharmaceuticals has signed an agreement with a clinical quality and validation processes consultancy to oversee the preparation and submission of a Pre-IND Meeting request to the FDA on its anti-tumor Drug Candidate CANNABICS™ RCC-33 ...
GI Supply Gets FDA Clearance for Submucosal Lifting Agent in Pre-filled 10mL Syringe americanpharmaceuticalreview
October 26, 2020
GI Supply announced the FDA clearance of EverLift™ Submucosal Lifting Agent in a 10mL syringe, a new device for the lift of polyps, adenomas, early-stage cancers and other gastrointestinal lesions prior to excision with a snare or other appropriate ...
Gilead gets USFDA approval for Veklury (remdesivir) to treat COVID-19 expresspharma
October 26, 2020
Gilead Sciences announced that the US Food and Drug Administration (FDA) has approved the antiviral drug Veklury (remdesivir) for the treatment of patients with COVID-19 requiring hospitalisation.
USFDA approves IND application from Reven Pharma for Rejuveinix to treat COVID-19 expresspharma
October 26, 2020
RJX is an IV formulation being developed for treatment of inflammatory disorders, including COVID-19 patients with viral sepsis, multi-system inflammation, cytokine release syndrome, shock, ARDS and multi-organ failure.
Second wave of COVID-19 vaccines may not be needed to reach higher efficacy bar than first batch expresspharma
October 26, 2020
It would be best for second wave vaccines to underscore ideal subpopulations or manufacturing and storage advantages that could underscore uptake.
Mexico may not follow FDA and approve remdesivir for COVID-19 expresspharma
October 26, 2020
WHO Solidarity drug trial last week concluded remdesivir has little or no impact on a patient’s chances of surviving COVID-19.
FDA approves first treatment for COVID-19 worldpharmanews
October 23, 2020
The U.S. Food and Drug Administration approved the antiviral drug Veklury (remdesivir) for use in adult and pediatric patients 12 years of age and older and weighing at least 40 kilograms (about 88 pounds) for the treatment of COVID-19 requiring hospitali
Granules India gets US FDA approval for potassium chloride ER tablets expresspharma
October 23, 2020
Granules announced that it has received marketing approval from the US FDA for Potassium Chloride Extended Release Tablets USP, 10 mEq (750 mg) and 20 mEq (1500 mg) for the treatment of patients with hypokalemia.
Aurobindo Pharma receives USFDA approval for Acetaminophen Injection expresspharma
October 23, 2020
It is indicated for the treatment of mild to moderate pain in adult and paediatric patients two years and older.
VENCLEXTA Receives FDA Approval for AML americanpharmaceuticalreview
October 22, 2020
AbbVie announced the U.S. Food and Drug Administration (FDA) has provided full approval to VENCLEXTA® (venetoclax) in combination with azacitidine, or decitabine, or low-dose cytarabine (LDAC) for the treatment of newly-diagnosed acute myeloid leukemia ..

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