Mesoblast - Increasingly positive on aGvHD
With a positive primary endpoint plus 180-day data in acute graft versus host disease (aGvHD), Mesoblast is on track for its first US approval. Mesoblast is targeting US approval in H120 for GvHD and other key clinical trial endpoints, such as in Class II–III congestive heart failure (CHF) and lower back pain, and over the next two years is set to transition, assuming clinical and market success, into a profitable pharmaceutical company.Mesoblast is engaged in the development of regenerative medicine products. Co. has leveraged its proprietary technology platform, based on specialized cells known as mesenchymal lineage adult stem cells ("MLCs"), to establish a portfolio of late-stage product candidates. Co.'s allogeneic, "off the shelf" product candidates target advanced stages of diseases with high, unmet medical needs including cardiovascular conditions, orthopedic disorders, immunologic and inflammatory disorders and oncology and hematologic conditions. Each MLC-derived product candidate has technical characteristics, target indications, reimbursement strategy, commercialization potential, and partnering opportunities.
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