Bharat Biotech begins human preliminaries for Covaxin, India’s first COVID-19 antibody Kumar Jeetendra | July 14, 2020 Bharat Biotech has started human trials on its vaccine offender,’Covaxin’. Covaxin, being developed by the Hyderabad-based bio tech business and Indian Council of Medical Research (ICMR) is now India’s first native COVID-19 vaccine. Bharat Biotech had said that it really is trying to build up a preliminary capacity of 200 million vials of the vaccine. …
Cipla receives final approval for generic version of Shire’s Firazyr® Kumar Jeetendra | July 14, 2020 Mumbai, India; July 14, 2020: Cipla Limited (BSE: 500087; NSE: CIPLA EQ; and hereafter referred to as “Cipla”) today announced that it has received final approval for its Abbreviated New Drug Application (ANDA) for Icatibant Injectable 30mg/3mL from the United States Food and Drug Administration (US FDA). Cipla’s Icatibant Injectable Pre-Filled Syringe 30mg/3mL is AP-rated …
Biocon’s accomplice Equillium plans Itolizumab’s worldwide clinical preliminary for COVID-19 Kumar Jeetendra | July 13, 2020 Biocon’s partner Equillium has said it is planning to conduct a global randomised controlled clinical trial of Itolizumab in COVID-19 patients, for the American biotech firm will record a US investigational new drug application (IND). Itolizumab, which is used for the treatment of psoriasis, is repurposed for COVID-19, as it regulates the production of inflammatory …
Pfizer, BioNTech’s coronavirus immunizations get FDA’s ‘most optimized plan of attack’ status Kumar Jeetendra | July 13, 2020 The candidates, both BNT162b1 and BNT162b2, would be the most complex of at least four vaccines getting analyzed by most firms in ongoing trials in the United States and Germany. Pfizer’s shares were up roughly 2% and U.S.-listed stocks of BioNTech were up roughly 6 percent before the bell. Earlier this month, the firms said …
Biocon tranquilize gets DCGI gesture for use in moderate to extreme COVID-19 patients Kumar Jeetendra | July 11, 2020 DCGI has vowed to market Itolizumab (ALZUMAb) injection 25mg and 5mL solution for emergency usage within India for the cure of cytokine release syndrome (CRS) at moderate to severe ARDS (acute respiratory distress syndrome) patients thanks to COVID-19, Biocon said in a release. It said Itolizumab is your first publication biologic therapy to become approved …
Gilead says Extra data on remdesivir Reveals improved clinical Retrieval Kumar Jeetendra | July 10, 2020 Gilead Sciences Inc said on Friday additional data from a late-stage study revealed its antibacterial remdesivir significantly enhanced clinical recovery from seriously ill COVID-19 patients. Findings from a study of its late-stage study revealed that 74.4 percent of remdesivir-treated patients recovered by Day 14 versus 59.0 percentage of individuals receiving standard of care, the business …
Research center testing affirms adequacy of BETADINE germicide items against SARS-CoV-2 Kumar Jeetendra | July 10, 2020 Mundipharma today announced that lab testing at the Duke NUS Medical School at Singapore, has confirmed the potency of its BETADINE® antiseptic services and products against the publication coronavirus (SARS-CoV-2) that causes COVID-19 disease. Testing has demonstrated BETADINE’s® strong in vitro virucidal exercise, killing 99.99% of the SARS-CoV-2 virus in 30 seconds. The investigation was …
Strides Pharma gains on USFDA endorsement Kumar Jeetendra | July 9, 2020 Strides Pharma Science climbed 1.28percent to R S 416.60 as a result of its Singapore-based subsidiary, Strides Pharma Global, received US FDA approval for butalbital, acetaminophen, caffeine, and codeine phosphate capsules. According to IQVIA MAT May 2020 statistics, the US market for butalbital, acetaminophen, caffeine, and codeine phosphate capsules, and 50 mg/325 mg/40 mg/30 mg, …
COVID-19 immunization: Premas Biotech starts mice examines Kumar Jeetendra | July 9, 2020 Premas Biotech, the Gurgaon-based Biotech organization which built up the triple antigen infection like molecule (VLP) immunization contender for SARS CoV-2 infection, said it had advanced into creature preliminaries. “The four-week fake treatment controlled, blinded and randomized tests to be directed in mice, will look to assess security in the rat display and analyze insusceptible …
Cipla dispatches nonexclusive rendition of remdesivir in India Kumar Jeetendra | July 9, 2020 Pharma important Cipla on Wednesday said it has launched its own generic version of antiviral drug remdesivir at a cost which is one of the lowest internationally and is seeking to supply over 80,000 vials over the first month. The company, however, did not disclose the purchase price of the medicine. Cipla had earlier said …
Unichem Laboratories gets USFDA gesture for Cyclobenzaprine HCI Tablets Kumar Jeetendra | July 8, 2020 Unichem Laboratories has gotten ANDA endorsement for its Cyclobenzaprine Hydrochloride Tablets USP, 5 mg, 7.5 mg and 10 mg from the United States Food and Drug Administration (USFDA) to showcase a nonexclusive rendition of FLEXERIL (Cyclobenzaprine HCI) Tablets, 5 mg and 10 mg of Janssen Research and Development LLC. Cyclobenzaprine HCI Tablets are shown for …
Baxter India gets CDSCO gesture for utilization of its Oxiris channel in COVID-19 treatment Kumar Jeetendra | July 7, 2020 Healthcare firm Baxter India on Tuesday said it has received consent from the Central Drugs Standard Control Organisation (CDSCO) for the usage of its Oxiris blood purification filter to the treatment of COVID-19 patients. The filter is meant to be utilised in the seriously ill COVID-19 patients needing blood purification where excess inflammatory mediators are …
