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July 21 (Reuters) - The European Medicines Agency's
panel declined to back authorization for Mirati Therapeutics'
MRTX.O drug to treat a type of lung cancer as it did not
fulfill the requirements for conditional support.
Mirati said on Friday it disagrees with the EMA's opinion
and intends to request a formal re-examination, but gave no
details on the requirements it did not fulfill.
Its drug, adagrasib, approved by the U.S. Food and Drug
Administration in December, is designed to target a mutated form
of a gene known as KRAS that occurs in about 13% of non-small
cell lung cancers, the most common form of the disease, and less
frequently in some other solid tumors.
(Reporting by Leroy Leo in Bengaluru; Editing by Shinjini
Ganguli)
((Leroy.Dsouza@thomsonreuters.com ; Twitter: https://twitter.com/LeroyLeo7;))