Novartis’s Capmatinib (INC280) Receives the US FDA’s Breakthrough Therapy Designation for MET-Mutated Advanced Non-Small Cell Lung Cancer

 Novartis’s Capmatinib (INC280) Receives the US FDA’s Breakthrough Therapy Designation for MET-Mutated Advanced Non-Small Cell Lung Cancer

Novartis Reports Results of QMF149 in P-III PALLADIUM Study for Patients with Uncontrolled Asthma

Shots:

  • The US FDA’s BT designation is based on GEOMETRY mono-1 study involves assessing of Capmatinib and the results were also updated in American Society of Clinical Oncology
  • The BT designation is granted to serious or life-threatening disease therapies demonstrate a substantial improvement over existing therapies on one or more significant preliminary research endpoints
  • Capmatinib (INC280) is an oral potent and selective MET inhibitor with expected regulatory submission in Q4’19. In 2009, Novartis signed an exclusive development and commercialization agreement with Incyte for Capmatinib

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