Janssen-Cilag International NV, a Johnson & Johnson company, today announced new data from the Phase 1b/2 OrigAMI-1 study, which showed amivantamab combined with chemotherapy (mFOLFOX6 [FOLFOX] or ...

Ozempic, a GLP-1 receptor drug originally produced to treat diabetes, has become the next star product of the multi-million ...

In the European Union, the FDA's equivalent organization is the European Medicines Agency ... is approved by the FDA on the agency's website via its Orange Book. FDA-approved drugs are also ...

This interview with Puja Myles, director, Clinical Practice Research Datalink (CPRD) in the Safety and Surveillance Group at ...

Tactics used to persuade U.S. doctors that potent painkillers could be safely prescribed have been used abroad, an ...

The first notable agency action in 2024 is the FTC’s Second Request in Novo Holding’s proposed $16.5 billion acquisition of Catalent, a life sciences contract manufacturer. 1 The agency’s interest in ...

A broad majority in the Copenhagen City Council on Monday reached an agreement on the municipality’s budget for next ...

After a week of extraordinarily warm September days, autumn comes to Denmark on Monday.On Monday morning, cloudbursts were ...

Opium also has innumerable beneficial uses, perhaps more so than any other psychoactive. It is precisely because of its ...

Rich countries have several hundred million doses of vaccines that could help fight an mpox outbreak in Africa, where donated shots fall far short of what is needed, according to a Reuters tally of ...

The European Medicines Agency also said that extra doses of the Moderna and Pfizer-BioNTech vaccines could be given to people with underlying health conditions as early as 28 days after a second dose.