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Unlocking the genetic code: The future of gene therapy for genetic disorders

What is gene therapy? Gene therapy acts as the lighthouse of contemporary medicine by offering to help correct hereditary afflictions at their very roots—the genome itself. Such treatment involves ...

The history and evolution of gene therapy

History and Evolution of Gene Therapy The history and development of gene therapy, a radically new medical intervention that intends to treat or prevent diseases by modifying the genetic material wit...

Gene therapy in China

Genetic disorders and gene therapy Gene therapy has transformed the concept of treatment for a genetic disorder, thus giving hopes to millions across the globe. Therefore, regarding biomedical resear...

FDA approves gene therapy to treat beta thalassemia

FDA approval of gene therapy The FDA has made it possible for people 12 years of age and older who have transfusion-dependent beta-thalassemia (TDT) to use exagamglogene autotemcel (Casgevy, Vertex)....

First gene therapy approved by the USFDA to treat sickle cell disease

USFDA approved gene therapy for sickle cell disease The U.S. Food and Drug Administration has granted approval for two significant medications, Casgevy and Lyfgenia, which are the first gene therap...

Gene Therapy for Thalassemia

Gene Therapy Applied to Thalassemia: An Overview Thalassemia is one such blood disorder characterized by the body being unable to produce enough hemoglobin, making life unusually challenging for both...

Repotrectinib has received accelerated approval from the USFDA for adult and pediatric patients with NTRK gene fusion-positive solid tumors

  June 2024: The Food and Drug Administration (FDA) has given accelerated approval to repotrectinib (AUGTYRO, Bristol-Myers Squibb Company) for the treatment of solid tumors in adult and pedia...

Imetelstat is approved by FDA for low- to intermediate-1 risk myelodysplastic syndromes with transfusion-dependent anemia

  May 2024: Imetelstat (Rytelo, Geron Corporation), an oligonucleotide telomerase inhibitor, has been approved by the Food and Drug Administration for use in adults with low- to intermediate-1...

Tovorafenib has been granted accelerated approval by the FDA for patients with relapsed or refractory BRAF-altered pediatric low-grade glioma

April 2024: The Food and Drug Administration (FDA) granted accelerated approval to tovorafenib (Ojemda, Day One Biopharmaceuticals, Inc.). This approval is specifically for patients aged 6 months and ...

Lutetium Lu 177 dotatate is approved by USFDA for pediatric patients 12 years and older with GEP-NETS

Lutetium Lu 177 dotatate is approved by USFDA for pediatric patients The Food and Drug Administration has approved lutetium Lu 177 dotatate (Lutathera, Advanced Accelerator Applications USA, Inc., a ...

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