NMDP BioTherapies to Present Data at ISCT 2024 on the Stability of Infectious Disease Marker Analytes During Donor Qualification for Allogeneic Cell Therapies

Study in conjunction with investigators from Labor Quade and the Johns Hopkins School of Medicine analyzed the longer-term stability of IDM analytes in uncentrifuged peripheral blood samples to allow for increased flexibility in donor sample processing. Study results indicate that broad use of blood processing parameters developed for the measure of metabolites appears to create…

NMDP BioTherapies Introduces Enhanced Cellular Materials for Allogeneic Cell Therapy Development

First of Its Kind Clinical-Grade Leukopak Now Facilitates Easier Regulatory Filing with Access to a DMF and Identification of Additional Characteristics Required to Qualify Cord Blood Units as Starting Material for Manufacture of Cell and Gene Therapies MINNEAPOLIS, April 16, 2024 — NMDP BioTherapiesSM (formerly known as the Be The Match BioTherapies), a leader in cell…

NMDP BioTherapies Appoints New President to Lead Next Phase in Life-Saving Therapy Development

Tom Hochuli will lead the organization as it renews its commitment to advancing cell and gene therapy MINNEAPOLIS , Jan. 30, 2024 — NMDP BioTherapies℠, formerly Be The Match BioTherapies, announced that Tom Hochuli will serve as president, leading the organization into its promising future phase. The appointment comes at a significant time for NMDP, which underwent…

International regulations for allogeneic cell source material

When you procure cellular starting material or distribute a cell or gene therapy product across international borders, you must consider the country or regional regulatory requirements at play and where they diverge. Allogeneic cell therapy sponsors face common challenges when treating a global patient population with therapies using healthy adult donor starting material.