FDA RMAT Designation Granted to GLPG5101 for the Treatment of R/R MCL
“This designation reflects the promising clinical activity and safety profile observed in our ongoing Phase 1/2 study and supports our commitment to delivering an effective and timely treatment option to patients in need,” said Omotayo Fasan, M.D., Clinical Development Program Head at Galapagos. “With RMAT status allowing for closer collaboration with the FDA, this will enable additional opportunities for accelerated development and assessment timelines.”
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