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Angiocrine Bioscience Announces Oral Presentation of Intravenous AB-205 Data during the Annual Transplantation & Cellular Therapy Meetings of ASCT and CIBMTR

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SAN DIEGO, Feb. 5, 2021 /PRNewswire/ Angiocrine Bioscience Inc., a clinical-stage biopharmaceutical company today announced that the American Society for Transplantation and Cellular Therapy (ASTCT) and the Center for International Blood & Marrow Transplant Research (CIBMTR) has selected Angiocrine s AB-205 Phase 1b/2 study results for an oral presentation. Intravenous AB-205 is being developed to treat diffuse damage of vascular niches of multiple organs caused by off-target cytotoxicity from high-dose chemotherapy (HDT) in the course of conditioning patients undergoing autologous hematopoietic cell transplantation to effect a cure of aggressive lymphomas. Treating the damaged vascular niches enable prompt repair of multiple organs. In case of HDT, the most severely and frequently affected organ systems are oral-gastrointestinal and hematopoietic. By enabling multi-organ repair, AB-205 has the potential of substantially reducing ....

United States , Lihua Budde , Johnr Jaskowiak , Paul Finnegan , Angiocrine Bioscience , Prnewswire Angiocrine Bioscience Inc , Drug Administration , Angiocrine Bioscience Inc , American Society For Transplantation , International Blood Marrow Transplant Research , Bioscience Inc , American Society , Cellular Therapy , International Blood , Marrow Transplant Research , Oral Abstract , Regimen Related Toxicity , Open Label Dose Escalation Trial , Lymphoma Undergoing High Dose Therapy , Autologous Hematopoietic Cell Transplantation , Severe Toxicities , Autologous Hematopoietic Cell Transplant , Regenerative Medicine Advanced Therapy , Orphan Drug Designation , ஒன்றுபட்டது மாநிலங்களில் , பால் ஃபிநிகெந் ,

Transplantation & Cellular Therapy Annual Meetings

Transplantation & Cellular Therapy Annual Meetings
Last Modified, February 05, 2021
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Medexus Pharmaceuticals and medac GmbH enter into a License Agreement for First-in-Class Conditioning Agent for Hematopoietic Stem Cell Transplantation, Treosulfan, in the United States

Medexus Pharmaceuticals and medac GmbH enter into a License Agreement for First-in-Class Conditioning Agent for Hematopoietic Stem Cell Transplantation, Treosulfan, in the United States
February 02, 2021 14:21 ET
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Medexus Pharmaceuticals Inc
Medexus Pharmaceuticals Inc
Orphan Designated Drug with August 2021 PDUFA date
Management to host conference call at 10:00 AM Eastern Time on February 3, 2021 and
Key Opinion Leader webinar to be held at 2:00 PM Eastern Time on February 5, 2021
TORONTO and CHICAGO and MONTREAL and WEDEL, Germany, Feb. 02, 2021 (GLOBE NEWSWIRE) Medexus Pharmaceuticals Inc. (“
Medexus”) (TSXV: MDP) (OTCQX: MEDXF)
(Frankfurt: P731) is pleased to announce that it and its wholly-owned United States-based subsidiary, Medexus Pharma, Inc. (“ ....

United States , Nordrhein Westfalen , H Joachim Deeg , Medexus Pharma , Miklos Kohary , Natalia Zimonyi Kohary , Tina Byers , Mary Horowitz , Roland Boivin , Marrow Transplant Research , Roberta Uihlein Professor Of Hematologic Research , Deputy Cancer Center , International Blood , International Blood Marrow Transplant Research , University Of Bonn School Medicine , Cancer Research , Medexus Pharmaceuticals , Professor Of Clinical Research , University Of Rochester , Seattle Cancer Care Alliance , University Of Washington School Medicine , Marrow Clinical Trials Network , Venture Exchange , Symphony Health , Regulation Services Provider , Medexus Pharma Inc ,