OCEANIC-AF is one trial which evaluates asundexian versus apixaban in patients with atrial fibrillation at risk for stroke within the overall OCEANIC phase III program
Emphasizes the need for a collective effort on bolstering resilience across economies, societies, healthcare systems, education systems and infrastructure
Approval based on results from TOPAZ-1 global Phase III trial and a Chinese patient
This product will be manufactured at Lupin’s Pithampur facility in India
The European Commission approved the use of Carbopol as an additive for liquid and solid food supplements in the EU
Approval based on DESTINY-Lung02 results where AstraZeneca and Daiichi Sankyo’s Enhertu demonstrated a confirmed objective response rate of 49% and median duration of response of 16.8 months in previously treated patients
New Molecular biology lab launched, AIIA increased its work scope in form of MoUs
Approval of oral, once-daily VELSIPITY based on favorable safety and efficacy data from the ELEVATE UC Phase 3 trials
The NDA filing for deuruxolitinib with the U.S. FDA is based on two pivotal Phase III trials
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