Japanese Regulators Approve Promega CDx for Merck's Keytruda

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Japanese Regulators Approve Promega CDx for Merck's Keytruda

Feb 05, 2019

NEW YORK (GenomeWeb) — Promega announced today that Japan's Ministry of Health, Labour, and Welfare has approved a companion diagnostic for Merck's cancer immunotherapy Keytruda (pembrolizumab) based on its microsatellite instability (MSI) technology.

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Japanese Regulators Approve Promega CDx for Merck's Keytruda

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