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Eye-care company agreed to pay $1.75 billion for Novartis’s dry-eye treatment Xiidra. → Read More
BioMarin’s gene therapy is the first to win Food and Drug Administration approval for adults with the most common form of the bleeding disorder. → Read More
The shot won FDA approval as a new study finds a 14-percentage-point drop in vaccine confidence since the Covid pandemic. → Read More
Health authorities and vaccine makers are moving toward targeting the next shot on a form of the XBB strain that is now circulating widely in the U.S. → Read More
Pfizer, one of the world’s biggest pharmaceutical companies, is flush with cash from the COVID-19 pandemic and hopes the Seagen acquisition will help grow revenue. → Read More
The agency has told vaccine makers to target the rapidly emerging Omicron subvariants BA.4 and BA.5, as well as the ancestral strain of the virus. → Read More
Approval of Paxlovid, which has been available under an Food and Drug Administration authorization for use during the pandemic, would allow Pfizer to market and sell it commercially. → Read More
One shot that was tested targeted Omicron specifically, while another was modified to work against the strain and the original virus. → Read More
The request for clearance of a three-dose series could lead to the young age group gaining access to Covid-19 shots as soon as this month. → Read More
Pfizer’s antiviral drug sees an uptick in prescriptions, as more doctors order patients take it over the Merck-Ridgeback pill called Lagevrio. → Read More
The arrangement means that some of the drugs that carry list prices of tens of thousands of dollars a year in the U.S. would be substantially less for the low-income countries to buy, according to Pfizer. → Read More
Merck, J&J and some other drugmakers are dialing back sales estimates now that supplies are ample and many people are vaccinated. → Read More
The three shots were found effective in preventing symptomatic Covid-19 in children 6 months to 5 years, an early analysis of study data found. → Read More
The authorization by U.S. health regulators expands booster access to about 28 million youngsters. → Read More
Some patients who took Paxlovid to treat Covid-19 have experienced cold-like symptoms such as sore throat and cough two weeks after appearing to get better, puzzling physicians and researchers trying to stay ahead of the virus. → Read More
The move to acquire the New Haven, Conn., biopharmaceutical company will give the New York drugmaker full ownership of the Nurtec migraine franchise. → Read More
Demand for the company’s antiviral pill has increased as Covid-19 cases have jumped. → Read More
Paxlovid, authorized to treat people at high risk of severe disease within a few days of infection, wasn’t found to prevent symptomatic infections in a study. → Read More
U.S. health regulators approved a pill from Bristol-Myers Squibb, the first to treat a genetic heart disease that is the most common cause of sudden cardiac death in people under age 35. → Read More
Pfizer Inc. and partner BioNTech SE said earlier this month that a third shot safely generated a strong immune response in the youngsters. → Read More