The HUB Foundation for Organoid Technology and STEMCELL Technologies Sign Agreement on the Manufacturing of Cell Culture Media for Organoids The HUB Foundation for Organoid Technology announced that it has signed a licensing agreement with STEMCELL Technologies Inc. for the manufacturing and worldwide distribution of cell culture media for growing Organoids. Organoids are mini-organs grown in tissue culture from small pieces of tissue derived from patients with cancer and other diseases, and represent an exciting new tool for scientific research and drug discovery and validation. [STEMCELL Technologies Inc.] Press Release Biocon Collaborates with Advaxis for ‘ADXS-HPV’: A Novel Cancer Immunotherapy Biocon Ltd. and Advaxis, Inc. announced that they have entered into an exclusive licensing agreement for co-development and commercialization of ADXS-HPV, a novel cancer immunotherapy for the treatment of human papillomavirus-associated cervical cancer in women, for India and key emerging markets. [Biocon Ltd.] Press Release MD Anderson Announces Collaboration with Johnson & Johnson Innovation on Cancer Immunotherapy The University of Texas MD Anderson Cancer Center will collaborate with Johnson & Johnson Innovation, LLC, and its affiliate Janssen Biotech, Inc., to develop immunology-based cancer treatments through the MD Anderson Moon Shots Program immunotherapy platform. [University of Texas M. D. Anderson Cancer Center] Press Release Regeneus Partners with Lonza for Manufacturing CryoShot Canine Cell Therapy Product for US FDA Trial Regeneus, announced that Lonza will manufacture Regeneus’ off-the-shelf cell therapy, CryoShot® Canine, for registration in the US. The cells will be manufactured at the Lonza facility in Walkersville, Maryland and then distributed to the participating trial veterinarian clinics. [Regeneus Ltd] Press Release Minister Sherlock Opens Ireland’s First Human Use Stem Cell Manufacturing Facility at NUI Galway The Centre for Cell Manufacturing Ireland at NUI Galway is the first ever facility on the island of Ireland to receive a license from the Irish Medicines Board to manufacture culture-expanded stem cells for human use. [National University of Ireland, Galway] Press Release California Stem Cell Submits Phase II Clinical Trial Protocol to FDA for Treating Ovarian Cancer California Stem Cell, Inc. (CSC) announced it has submitted a Phase II protocol to the U.S. Food and Drug Administration for a randomized, double-blind study to evaluate CSC’s patient-specific cancer immunotherapy in women with Stage III or IV ovarian, fallopian tube or primary peritoneal cancer. [California Stem Cell, Inc.] Press Release TotipotentRX Corporation and ThermoGenesis Corp. Report Statistically Significant Phase Ib Clinical Trial Results in Critical Limb Ischemia ThermoGenesis Corp. and TotipotentRX Corporation announced their co-sponsored Phase Ib clinical trial safety and efficacy results treating no-option patients suffering from critical limb ischemia with Totipotent’s CLIRST (Critical Limb Ischemia Rapid Stem cell Therapy) treatment. [ThermoGenesis Corp.] Press Release BioLineRx Receives Orphan Drug Designation for Novel Stem Cell Mobilization Treatment BioLineRx announced that it has received notice from the U.S. Food & Drug Administration confirming an Orphan Drug Designation of BL-8040 as a treatment for stem cell mobilization, in addition to the Orphan Drug Designation previously granted to BL-8040 as a treatment for acute myeloid leukemia. [BioLineRx] Press Release apceth’s Ground-Breaking First-in-Man, First-in-Class Clinical Trial in Oncology with Genetically Modified Mesenchymal Stromal Cells Is Now Enrolling apceth announced that the TREAT ME Phase I/II clinical trial for patients suffering from advanced adenocarcinoma of the gastro-intestinal tract has commenced. This is the first clinical trial world-wide with genetically-modified mesenchymal stromal cells. [B3C Group GmbH] Press Release Pluristem’s Cell Manufacturing Facility Marks Major Milestone with German Regulatory Approval of New Scaled-Up 3D Manufacturing Process Pluristem Therapeutics, Inc. announced it has received approval from the Paul-Ehrlich-Institute, Germany’s health authority, to supply cells from its advanced, fully automated, and proprietary 3D cell expansion manufacturing platform implemented at its new state-of-the-art GMP facility. [Pluristem Therapeutics Inc.] Press Release Bioheart Announces Exclusive License in Veterinary Medicine for Patents for Cancer-Related Immunotherapy Products Bioheart, Inc. announced that it has entered into an agreement to license three different cellular based immunotherapy patents from inventor Allan Wu, M.D. [Bioheart, Inc.] Press Release |