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Pfizer reports topline data from SigVie-002 study for NSCLC
The trial enrolled 703 participants who had previously received one or more lines of systemic therapy.
Things are going from bad to worse for the pharmaceutical giant.
A post-marketing trial finds the oral antiviral achieves effective blood concentrations in at-risk children aged 6 years or older with mild-to-moderate COVID.
Pfizer (NYSE:PFE) oncology updates and IBRANCE expansion unfold within S&P 500 healthcare segment, alongside lung cancer ...
The study was originally meant to be published in a CDC weekly report in March.
Patients who had received only one prior line of systemic therapy showed a stronger trend for overall survival and ...
Volatility can lower the cost of entry into businesses that throw off real cash, even as investors recognize that a low share ...
Pfizer (PFE) stock is in focus as the FDA approves a label expansion therapy for breast cancer therapy, palbociclib, marketed ...
In the past two weeks, CARsgen Therapeutics won the world's first regulatory approval for a solid tumor CAR-T Biologics' ...
A comprehensive new review published in The Lancet affirms that currently approved mRNA vaccines are safe and highly ...
A bipartisan group of U.S. lawmakers opened national security investigations into whether five drugmakers including Merck and ...
(NYSE: PFE) today announced the U.S. Food and Drug Administration (FDA) approved IBRANCE ® (palbociclib) in combination with trastuzumab, with or without pertuzumab, and endocrine therapy for the ...
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