In bestowing the pro-housing label on San Francisco, the Department of Housing and Community Development (HCD) said the city ...

Cabozantinib is the active ingredient in two of Exelixis' three approved drugs (Cabometyx and Cometriq) and its strongest US patent covering cabozantinib’s composition of matter expires in 2030.

Yale surgeons have completed Connecticut’s first FDA-approved TAMBE procedure, marking a shift in the treatment of complex ...

With the data under review by the FDA, experts estimate that a substantial population could potentially benefit.

Basel, October 29, 2024 – Novartis announced today that Scemblix ® (asciminib) was granted accelerated approval by the US Food and Drug Administration (FDA) for adult patients with newly diagnosed ...

The FDA granted an accelerated approval to asciminib for newly diagnosed Ph+ chronic myeloid leukemia in the chronic phase.

After the recent FDA approval for the promising schizophrenia drug Cobenfy (xanomeline and trospium chloride), Bristol Myers ...

Wilson Encourages Investors Who Suffered Losses Exceeding $100,000 In Elanco To Contact Him Directly To Discuss Their Options If you suffered losses exceeding $100,000 in Elanco between November 7, ...

This site displays a prototype of a “Web 2.0” version of the daily Federal Register. It is not an official legal edition of the Federal Register, and does not replace the official print version or the ...

When a doctor prescribes a medication for a use other than one that has been approved by the FDA, it’s known as off-label use. Doctors prescribe off-label for several reasons including ...

Off-label means that, when appropriate, a doctor prescribes a drug for a condition or at a dosage that the FDA has not approved. There has been a shortage of Mounjaro since its approval in 2022.