I love hearing the stories of patients discharged within days. Just stop and think about that for a moment. People on death's door, getting discharged days later!! That is unheard of in medical practice.
Its been a hard slog, but MSB are so close now. Experienced bio-tech holders would have told you regulatory approval is a tricky hurdle, but few would have called the GvHD decision. It will be a temporary delay.
I am the recipient of two successful stem cell procedures (tenocyte stem cells in a tendon and mesenchymal in the shoulder labrum - cartilige/tendon mix so tenocyte stem cells inappropriate.
Within ten years tenocyte stem cells will be the gold start treatment for tendons, chondrocyte stem-cells for cartilige and mesenchymal stem-cells in a host of inflammatory and other conditions. Patients with unmet needs will have options. This is a watershed time in history that MSB will be the bastion of.
Ann: COVID-19 ARDS & GVHD Update, Quarterly Report & Appendix 4C, page-53
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