FDA Acknowledges Pain Reduction Data Supporting Rexlemestrocel-L Efficacy
The US Food and Drug Administration (FDA) has acknowledged clinical data showing that Rexlemestrocel-L reduced pain intensity over 12 months, supporting the product’s efficacy in treating back pain. The agency also indicated that the approval label may include language related to opioid reduction.
Rexlemestrocel-L | 19/01/2026 | By News Bureau
Mesoblast Launches FDA-Approved Ryoncil for Pediatric Graft Versus Host Disease
Mesoblast has announced the commercial launch of Ryoncil (remestemcel-L-rknd) in the United States for the treatment of steroid-refractory acute graft versus host disease (SR-aGvHD) in pediatric patients aged two months and older.
Rexlemestrocel-L | 15/09/2025 | By Dineshwori | 142
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