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Bristol Myers Squibb to Present Data at ASCO & EHA from More Than 130 Studies Across 25 Diseases Supporting Expansion into New Indications, Demonstrating Long-Term Survival, and Highlighting Novel Modalities and Research Platforms

Bristol Myers Squibb (NYSE: BMY) today announced the presentation of data across its oncology and hematology portfolio at the upcoming 2024 American Society of Clinical Oncology (ASCO) Annual Meeting ....

United States , South Korea , Pushkar Mutha , Mariat Bourlon , Tycel Jovelle Phillips , Tony Mok , Lin Wang , Peter Robert Galle , Charlene Mantia , Marc Hoffmann , Eric Christenson , Suzanne Trudel , Manali Kirtikumar Kamdar , Guillermo Garcia Manero , Martin Reck , Tina Cascone , Jonathan Spicer , Elena Elimova , Jeremy Abramson , Bristol Myers Squibb , Daniel Lin , Williamg Wierda , Andrewh Wei , Ian Chau , Francesco Passamonti , Antonis Kattamis ,

PK Modulator Shows Promise in Thalassemia

In small study, mitapivat increased hemoglobin in 80% of non-transfusion-dependent patients ....

United States , Mike Bassett , Antonis Kattamis , Kevinhm Kuo , University Of Toronto , Kapodistrian University Of Athens School Medicine , Kapodistrian University , Athens School , North America ,

Outcomes in Nontransfusion-Dependent β-Thalassemia With Luspatercept or Placebo

Researchers determined luspatercept may improve outcomes in patients with nontransfusion-dependent β-thalassemia. ....

United States , Antonis Kattamis , American Society Of Hematology , Item Short Form Health Survey , University Of Athens , American Society , Annual Meeting , Reported Outcomes , Component Summary , Patient Global Impression ,

Bristol Myers Squibb to Highlight More than 80 Abstracts at ASH 2021 Demonstrating Strength of Innovative Therapeutic Platforms Improving Outcomes for a Broad Range of Hematologic Diseases

Bristol Myers Squibb to Highlight More than 80 Abstracts at ASH 2021 Demonstrating Strength of Innovative Therapeutic Platforms Improving Outcomes for a Broad Range of Hematologic Diseases
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United States , Idecabtagene Vicleucel Karmma , Yumi Nakayama , Maciej Garbowski , Christopher Parker , Leslie Kean , Uwe Platzbecker , Henry Chan , Paula Rodriguez Otero , Vikas Gupta , Nina Shah , Antonis Kattamis , John Godwin , Idecabtagene Vicleucel , Jeremy Abramson , Bristol Myers Squibb , Sundar Jagannath , Hemophagocytic Lymphohistiocytosis , Jean Marie Michot , Franck Morschhauser , Lisocabtagene Maraleucel , Jerill Thorpe , Michel Delforge , Manali Kamdar , Paul Richardson , Julien Lazarovici ,

CRISPR technology to cure sickle cell disease at UIC

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University of Illinois Chicago is one of the U.S. sites participating in clinical trials to cure severe red blood congenital diseases such as sickle cell anemia or Thalassemia by safely modifying the DNA of patients blood cells.
The first cases treated with this approach were recently published in an article co-authored by Dr. Damiano Rondelli, the Michael Reese Professor of Hematology at the UIC College of Medicine. The article reports two patients have been cured of beta thalassemia and sickle cell disease after their own genes were edited with CRISPR-Cas9 technology. The two researchers who invented this technology received the Nobel Prize in Chemistry in 2020. ....

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