FDA Approves Merck’s Pimjetmi for Tenosynovial Giant Cell Tumor

• FDA approved Merck KGaA’s PIMJETMI for adults with symptomatic tenosynovial giant cell tumor when surgery risks worsening functional limitation or severe morbidity.
• The once-daily oral treatment achieved a 56% objective response rate at week 25 versus 3% for placebo in Phase 3 testing.

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