Company profile

MESOBLAST LTD

NASDAQ:MESOBiotechnology: Biological Products (No Diagnostic Substances)

Drug pipeline (2)

AssetStageRevenueTrialsStatus
RYONCILapproved—0—
REMESTEMCEL-Lphase3—9no active trials

Revenue is the latest quarter the company reported for that product, from SEC filings; a fourth quarter is the year less nine months when no filing states one. Trial counts are of the product's ingredients, deduplicated by trial, so products sharing an ingredient share trials.

Clinical trials (34)

NCT IDPhaseStatusStartCompletionSponsor nameTitle
NCT01851070phase2completed2013-07-012016-05-01Mesoblast, Ltd.A Multi-center Study a Single IV Infusion of Allogeneic MPCs in Patients With Rheumatoid Arthritis and Incomplete Response to at Least One TNFα Inhibitor
NCT00225095phase1_2completed2005-09-012008-04-01Mesoblast International SàrlA Phase I/II Study of Chondrogen Delivered by Intra-Articular Injection Following Meniscectomy
NCT00721045phase2completed2008-08-012011-06-01Mesoblast, Ltd.A Phase II Dose-escalation Study to Assess the Feasibility and Safety of Transendocardial Delivery of Three Different Doses of Allogeneic Mesenchymal Precursor Cells (MPCs)in Subjects With Heart Failure
NCT02336230phase3completed2015-06-042018-04-09Mesoblast, Inc.A Prospective Study of Remestemcel-L, Ex-vivo Cultured Adult Human Mesenchymal Stromal Cells, for the Treatment of Pediatric Participants Who Have Failed to Respond to Steroid Treatment for Acute Graft-Versus-Host Disease (aGVHD)
NCT07568535phase3not_yet_recruiting2026-08-312028-02-28Mesoblast, Ltd.A Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase III Trial of Remestemcel-L-rknd Added to Ruxolitinib for Grade III-IV Steroid-Refractory Acute Graft-Versus-Host Disease

FDA applications (1)

ApplicationApprovedTypeApplicantProducts
BLA 1257062024-12-18BLAMESOBLAST, INC.