Washington [US], May 19 (ANI): US President Joe Biden on Wednesday (local time) invoked the Defense Production Act to ramp up the production of infant formula in the wake of growing safety concerns over quality of infant foods following death of two babies and subsequent shortage caused by supply chain bottlenecks.
Seoul [South Korea], May 12 (ANI/Global Economic): NeoImmuneTech said on the 11th that it has obtained the approval for a phase 2 clinical trial plan that concomitant administration of US Merck's immune checkpoint inhibitor Keytruda and its T-cell amplifier NT-I7 to patients with glioblastoma from the United States Food & Drug Administration (US FDA).
U.S. regulators on Thursday strictly limited who can receive Johnson & Johnson’s COVID-19 vaccine The restriction was due to a rare but dangerous risk of blood clots. The vaccination should only be administered to people who are unable to obtain another vaccine or who specifically prefer J&J’s vaccine, according to the FDA. For months, US […]
San Diego (California) [US], April 29 (ANI): According to a new study, chronic pain spinal cord stimulation (SCS) uses an implanted device to supply a small amount of electricity directly to the spinal cord, altering or blocking nerve activity and minimizing the sensation of pain reaching the brain.
China's President Xi Jinping is in a bind over who's to blame for Shanghai's virus outbreak. An obvious scapegoat is one of his close allies. https://t.co/WRsnDKnKSy China’s President Xi Jinping is in a Bind over Who’s to Blame for Shanghai’s Virus … – Latest Tweet by Bloomberg — Bloomberg (@business) April 29, 2022 Eli Lilly […]
Eli Lilly will ask the FDA for accelerated approval of its experimental Alzheimer’s treatment before July https://t.co/XKL1y7oO8n Eli Lilly Will Ask the FDA for Accelerated Approval of Its Experimental Alzheimer’s … – Latest Tweet by Bloomberg — Bloomberg (@business) April 28, 2022 Gujarat Shocker: Class 9 Student of Kendriya Vidyalaya Forced To Drink Urine by […]
A COVID-19 diagnostic test has come to light that uses breath samples to generate a positive or negative result. It has received emergency use authorization from the US Food and Drug Administration (FDA). Dubbed ‘InspectIR’, this breath analyzer COVID-19 test detects chemical components linked to coronavirus in breath samples. “Today’s authorization is yet another example […]
Austin (Texas) [US], April 13 (ANI/PRNewswire): Direct Biologics, an innovative biotechnology company with a groundbreaking extracellular vesicle (EV) platform drug technology, announced that the U.S. Food and Drug Administration (FDA) has awarded their EV drug product ExoFlo with a Regenerative Medicine Advanced Therapy (RMAT) designation for the treatment of Acute Respiratory Distress Syndrome (ARDS) associated with COVID-19.
New Delhi [India], April 7 (ANI/NewsVoir): The shift in purchasing power and technology may have made our lives easier and faster - but has it made our lives better? Well, not 100 per cent, if you ask me. In fact, we are left with over-exploited resources, tighter schedules, and little to no physical activity. A result of which is a variety of lifestyle diseases.