Vertex and CRISPR Therapeutics gain FDA approval for CASGEVY - World’s first sickle cell treatment using CRISPR gene editing technology
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Vertex and CRISPR Therapeutics gain FDA approval for CASGEVY - World’s first sickle cell treatment using CRISPR gene editing technology
Vertex and CRISPR Therapeutics have announced FDA approval for CASGEVY in treating sickle cell disease. Utilizing cutting edge CRISPR/Cas9 gene editing technology, a patient’s own genes are extracted, edited, and then reinserted to eliminate sickle cell in this new therapy.
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Bahrain This Week on Instagram: "His Royal Highness Prince Salman bin Hamad Al Khalifa, the Crown Prince and Prime Minister, visited the Royal Medical Services - Bahrain Oncology Center today, where he met the world’s first sickle cell disease patient outside the United States to successfully complete treatment with Casgevy (exagamglogene autotemcel). This groundbreaking CRISPR-based gene-editing therapy, utilizing bone marrow transplantation technology, marks a significant milestone in Bahrain’
Bahrain This Week on Instagram: "His Royal Highness Prince Salman bin Hamad Al Khalifa, the Crown Prince and Prime Minister, visited the Royal Medical Services - Bahrain Oncology Center today, where he met the world’s first sickle cell disease patient outside the United States to successfully complete treatment with Casgevy (exagamglogene autotemcel). This groundbreaking CRISPR-based gene-editing therapy, utilizing bone marrow transplantation technology, marks a significant milestone in Bahrain’
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FDA greenlights first gene-editing treatment, Casgevy, for sickle cell disease
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The US Food and Drug Administration approved two treatments, Casgevy and Lyfgenia, representing the first cell-based gene therapies for treating sickle cell disease (SCD) in patients 12 years and older. This video highlights the Casgevy treatment option. Treatment of SCD typically is lifelong and has multiple aspects ranging from managing symptoms and vasoocclusive episodes, preventing infections, pa!n control, and even blood transfusions. Before this new development, a “bone marrow transplant”
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The US Food and Drug Administration approved two treatments, Casgevy and Lyfgenia, representing the first cell-based gene therapies for treating sickle cell disease (SCD) in patients 12 years and older. This video highlights the Casgevy treatment option. Treatment of SCD typically is lifelong and has multiple aspects ranging from managing symptoms and vasoocclusive episodes, preventing infections, pa!n control, and even blood transfusions. Before this new development, a “bone marrow transplant”
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FDA greenlights first gene-editing treatment, Casgevy, for sickle cell disease
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FDA greenlights first gene-editing treatment, Casgevy, for sickle cel…
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