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news.Progenics’ Azedra gets FDA approval for rare adrenal gland tumors
The approval is for the intravenous use of the Azedra injection in patients whose adrenal gland tumors are unresectable and have spread beyond the original tumor site and
The approval is for the intravenous use of the Azedra injection in patients whose adrenal gland tumors are unresectable and have spread beyond the original tumor site and
Under the financial terms, Kite will provide research and development (R&D) funding for the collaboration and Gadeta will be eligible to receive future payments upon achievement of certain
The primary endpoint of the trial was defined as time to first occurrence of cardiovascular death, non-fatal myocardial infarction or non-fatal stroke (3-point MACE). Tradjenta had shown similar
Under the deal, Novartis will acquire the exclusive global development and marketing rights to MOR106 for atopic dermatitis and all other potential indications. Based on the achievement of
Janssen Sciences Ireland is a subsidiary of Janssen R&D Ireland. Sylvant has approvals for the treatment of idiopathic multicentric Castleman’s disease (iMCD) in more than 40 countries such as
The study showed that patients who secured two doses of tanezumab separated by eight weeks experienced a statistically significant improvement in pain, physical function and the patients’ overall
Financial details have not been disclosed. Proleukin® is licensed in around 20 countries around the world and is primarily indicated for use in metastatic renal cell carcinoma, as
Baloxavir marboxil was discovered by Shionogi & Co. and is being developed globally by the Roche Group (which includes Genentech in the US) and Shionogi & Co. The drug
The US District Court for the District of New Jersey has granted PI against DRL to stop selling or importing its generic buprenorphine/naloxone sublingual film product. Indivior also
TPOXX is claimed to be the first drug with an indication for treatment of smallpox, which is a contagious and fatal infectious disease. The approval of small-molecule antiviral