To apply cord blood market research to business decisions, a thorough understanding of the marketplace is required. There are a number of emerging trends, perinatal tissue types, and cell expansion technologies that are affecting the marketplace, but to fully understand their impact, historical context must be introduced. The global cord blood industry came into existence in the early 1990’s with the formation of several leading cord blood banks in the USA, followed by the establishment of cord blood banks across the globe. The mid-2000s were a growth period for the U.S. cord blood market, but that trend has since subsided and the market in now in a phase of maturation and consolidation. [Read more…]
PlumCare Announced Partnership With Cordlife and Additional Funding to Scale Operations
New agreement with Cordlife expands testing and monitoring service to eight new countries in Asia as company helps families make better decisions for their long term health
ALAMEDA, Calif., Feb. 28, 2018 — PlumCare, a DNA advisory service for families, today announced the company reached a partnership agreement with Cordlife Group Limited, a Singapore Exchange mainboard listed consumer healthcare company, as it expands access to the first-ever lifetime DNA testing and advisory service to help families take control of their health. To further support commercialization and access to its proprietary tests and services, PlumCare has secured an additional $750,000 in seed funding, with Steuart Ventures as the lead investor in this early stage financing round. [Read more…]
Cord Blood Industry Survival May Depend on Mass Affordability of Treatments Through Specialized Insurance Coverage
[Alexandra Romero, Guest Author] Recently, I had the opportunity to attend one of the largest events related to the Stem Cell and Regenerative Medicine Industry – Phacilitate/World Stem Cell Summit 2018. During the Plenary Super Session, Co-Chair Anthony Davies heavily discussed on a series of “fireside chats” the extremely high cost of some of the new stem cell-based treatments that have been recently approved. These conversations set the tone for one of the most discussed topics throughout the conference that gathered a great number of leaders not only from the medical and research fields, but also from the business sector. The “elephant in the room” seemed to finally be acknowledged, at least to some extent.
On the other hand, at the Cord Blood and Perinatal Stem Cells sessions, the big question on everybody’s mind was whether there is anything remarkably new and promising in the horizon that will allow the industry to stop its slow but steady decline caused by the lack of recent advancements. It was clear to the attendees (cord blood banks, investors, and research scientists), that the market has been experiencing a slow and chronic decline over the past 5 years, and there is a serious need to offer more options in terms of innovative and accessible treatments in order for the industry to remain sustainable in upcoming years. There has been a rapid evolution in the sources to obtain and utilize stem cells, which have been thoroughly addressed by Bioinformant in previous articles. [Read more…]
Cellenkos Achieves FDA Registration of GMP Manufacturing Facility for Cord Blood-Derived Therapeutics
Cellenkos, Inc. Announces FDA Registration of GMP Manufacturing Facility for Universal Donor Cell Therapeutics Derived from Cord Blood
HOUSTON, Feb. 6, 2018 — Cellenkos, Inc., a clinical-stage biotechnology company focused on developing universal donor cell therapeutics derived from cord blood (CB) for the treatment of autoimmune diseases and inflammatory conditions, today announced the successful registration of its stand-alone, manufacturing facility as GMP (good manufacturing practice) compliant with U.S. Food and Drug Administration (FDA). [Read more…]
Magenta Therapeutics’ Expanded Stem Cell Product, MGTA-456, Engrafts in 100% of Patients
– Data show rapid and durable engraftment with MGTA-456, an expanded cord blood stem cell product, in all 18 patients with hematologic malignancies across all conditioning regimens tested –
– MGTA-456 achieves clinical benefits of cord blood transplant –
– Clinically validated process to expand the numbers of CD34+ cells by >300 fold in single cord blood units significantly increases probability of identifying better HLA-matched stem cell donors for patients
December 11, 2017, CAMBRIDGE, Mass.–Magenta Therapeutics, a biotechnology company developing therapeutics to improve and extend the use of curative bone marrow transplant for more patients, today reported Phase 2 clinical data from its MGTA-456 hematopoietic stem cell (HSC) expansion program at the 59th annual meeting of the American Society of Hematology (ASH) in Atlanta, Ga. MGTA-456 is a single umbilical cord blood unit expanded with an aryl hydrocarbon receptor (AHR) antagonist. It is currently being studied in adult and pediatric patients with hematologic malignancies.
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