Search result for US FDA
ChemoCentryx's Avacopan, gets U.S. FDA approval for treating rare autoimmune disease
Highlights
- Avacopan gets approval from US FDA
- This drug is used to treat antineutrophil cytoplasmic antibody associated vasculitides
ChemoCentryx Inc, lead drug for treating a rare, fatal autoimmune disease has been approved by the U...
Australian firm Ellume recalls at least 200,000 at-Home Covid-19 test kits, over false positives
Highlights
- Ellume recalls almost 200,000 at-home Covid-19 tests from the US
- The US FDA issued an alert on Tuesday
Ellume, an Australian medical tech manufacturer has recalled almost 200,000 at-home Covid-19 tests. These kits have bee...
US FDA approves Pfizer's covid-19 vaccine
Pfizer’s corona virus vaccine gets complete authorization. This is a two-dose vaccine, and the two jabs are given three weeks apart from each other.
Janet Woodcock, the Commissioner of FDA said that, people can be very confident about the effectiveness...
BIOGEN'S ALZHEIMER’S DRUG RECEIVES APPROVAL FROM US FDA
In a historic move, the U.S. Food and Drugs Administration (FDA) on Monday granted approval to Biogen Inc's Aducanumab, a drug which happens to be the first against the Alzheimer's disease.
This new drug Aducanumab, that was heavily criticised by a certain section of medical expert...
US FDA GRANTS EUA TO GSK'S DRUG THAT TREATS MILD COVID-19 IN PEOPLE ABOVE 12
Highlights
• The GSK said this drug called VIR-7831 or Sotrovimab was cleared by the U.S. Food and Drug Administration for people ageing over 12
According to the statement issued by drugmaker GSK, the US FDA has granted Emergency Use Authorisation to a drug called S...
US FDA GRANTS EMERGENCY USE AUTHORISATION TO AMAZON'S COVID-19 TEST KIT
Highlights
• Amazon is now planning to use the real-time RT-PCR Test for detecting SARS-CoV-2. This is also part of it's overall preparedness and response programme
• “Amazon real-time RT-PCR test for detecting SARS-CoV-2 will be performed at laboratories d...
US FEDERAL HEALTH OFFICIALS SAYS ASTRAZENECA MAY HAVE USED OUTDATED DATA IN COVID-19 VACCINE TRIAL
Highlights
• In a statement issued on late Monday, the Data and Safety Monitoring Board said that it was concerned that the UK-based drugmaker may have provided an incomplete view of the efficacy data
• AstraZeneca had published the first data from an interim safety ...
JOHNSON & JOHNSON COVID VACCINE AUTHORIZED BY THE US FOR EMERGENCY USE
Highlights
• Courtesy of this approval, Johnson & Johnson's shot became the third vaccine to battle the COVID-19 pandemic in the United States
• President Joe Biden in his statement said that “This is exciting news for all Americans, and an encouraging ...
ALEMBIC PHARMA UNIT UNDER THE SCANNER OF US FDA FOR QUALITY CONTROL & EQUIPMENT ISSUES
Highlights
• The US FDA had recently issued a ‘Form 483’ to the Karkhadi unit of Alembic Pharma with five observations
• The FDA issues a ‘Form 483’ in which its inspectors enlist violations of good manufacturing practices by them at the time ...
US FDA GRANTS EMERGENCY USE AUTHORIZATION TO ELI LILLY'S ANTIBODY COCKTAIL FOR COVID-19
Highlights
• The company has said that the new treatment adds etesevimab or LY-CoV016 to bamlanivab or LY-CoV555, which has already been authorized, in order to make a double-antibody version
• Similar kind of dual antibody-cocktail is already available in the market...
DISTRIBUTION OF MODERNA’S COVID-19 VACCINE STARTS IN THE U.S.
Highlights
• Days after receiving emergency use authorization (EUA) from the US Food and Drug Administration (FDA), the distribution of the COVID-19 vaccine developed by Moderna Inc. has already started
• As per Moncef Slaoui, Chief of Operation Warp Speed, the first...
Pfizer SEEKING THE EMERGENCY USE TAG FROM THE U.S. FOR ITS COVID-19 VACCINE
Highlights
• If the emergency use tag is granted, the COVID-19 vaccine is likely to be available as early as next month said Pfizer
• The decision now lies with the US Food and Drug Administration (FDA) in order to permit the emergency use of the vaccinations
...Corp. Cell MedX. Provides updates to the company
Cell MedX Corp., a biotech company dedicated to discovering, developing and marketing therapeutic and non-therapeutic products that encourage overall well-being, is excited to provide a corporate update to its shareholders. Certifications The Company obtained a Certificate of Conformity for th...