Merck's tulisokibart met endpoints in Phase 3 UC study
The anti-TL1A antibody showed clinical remission at 12 weeks, with no safety concerns identified.
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Research-intensive biopharmaceutical company
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In short: Merck secured several FDA approvals for vaccines and cancer therapies, while expanding its oncology and animal health portfolios through strategic deals.
The anti-TL1A antibody showed clinical remission at 12 weeks, with no safety concerns identified.
The vaccine is indicated for children aged 2-17 with increased pneumococcal disease risk, adding serotype coverage.
Approvals add WELIREG combinations for adjuvant treatment of intermediate‑high or high‑risk ccRCC after nephrectomy. Based on Phase 3 LITESPARK‑022 showing 28% reduced risk of recurrence, metastasis or death.
The acquisition includes TARGAN's biodevice technology for poultry performance improvement.
Before its fifty percent surge, the drug giant was repeatedly telling a story about its future that the market seemed to be ignoring.
Merck (NYSE:MRK) received FDA approval for expanded use of KEYTRUDA and KEYTRUDA QLEX with WELIREG as adjuvant treatment in certain renal cell carcinoma patients. The...
, opens new tab said on Monday its experimental drug met the main goal and key secondary goals in a ...
XLV falls as Moderna surges; CMS drug-price rule pressures Merck and J&J; Lilly and Biogen announce deals.
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