Cipla Launches Generic Pomalidomide Capsules in the US
Cipla continues to expand its generic portfolio in the US with the launch of pomalidomide capsules for the treatment of adult patients with multiple myeloma.
Cipla continues to expand its generic portfolio in the US with the launch of pomalidomide capsules for the treatment of adult patients with multiple myeloma.
Following confirmation of the PDUFA target action date of April 30, 2027, Kowa anticipates a US commercial launch of the K-911 glaucoma eye drop in the second half of 2027, subject to FDA approval.
If approved, Jemperli could eliminate the need for chemotherapy, radiation, and surgery for some patients with dMMR/MSI-H locally advanced rectal cancer, said GSK.
Abbott’s Libre Duo 10 Day provides real-time glucose readings for daily diabetes management while continuously monitoring ketone levels in the background.
Developed by Lakefront in collaboration with Gilead Sciences, gamgertamig was previously granted both Fast Track and Orphan Drug Designation by the US FDA for the treatment of autoimmune haemolytic anaemia and immune thrombocytopenia.
Amygdala Neurosciences is initially developing ANS-858 as a potential treatment for alcohol use disorder and other substance use disorders.
With the unit classified as VAI, Aurobindo Pharma said pending applications for multiple inhalers and other dosage forms filed from the facility can now progress through the USFDA’s review process.
Lilly is calling on regulators, customs agencies, law enforcement authorities, online platforms, and payment companies to shut down the illegal retatrutide black market.
Aurobindo Pharma said the warning letter to Unit I of Eugia Pharma Specialities will have no impact on existing supplies to the US market.
Fresenius Kabi is notifying distributors and customers directly about the recall and is arranging for the return of affected products.