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Gene Editing for Haematological Disorders

This session examines the use of gene editing technologies (such as CRISPR-Cas9) to cure haematological illnesses like thalassemia and sickle cell disease. Correcting the genetic variations causing these conditions through gene editing may allow patients to receive curative medicines to enhance their quality of life.

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Innovations in Gene Editing
The Cell Therapy in Cancer Treatment
Ethical Considerations in Germline Gene Editing
Stem Cell Therapy: From Bench to Bedside
Ex Vivo Gene Editing: Techniques, Applications, and Challenges
Manufacturing Challenges in Cell and Gene Therapy
Clinical Trials and Real World Applications of Gene Therapy
Overcoming Challenges in AAV Based Gene Therapy
Ethical Considerations in Genetic Engineering and Therapy
Gene Therapy for Neurodegenerative Diseases
Advancements in Non Viral Gene Delivery Systems
Cell Therapy Manufacturing: Overcoming Scalability Issues
Gene Editing for Haematological Disorders
Future Trends: AI and Machine Learning in Cell and Gene Therapy Development
Immune System Modulation and Cell Therapy: Balancing Efficacy and Safety
Longitudinal Studies of Cell and Gene Therapy Outcomes
Non Viral Gene Delivery Strategies
Pharmacovigilance in Cell and Gene Therapy
Advances in CAR T Cell Therapies
Manufacturing and Process Analytics in Cell and Gene Therapy
Gene Editing for Haematological Disorders
Hematopoietic Stem Cell based Cell and Gene Therapy
Data Integrity and Clinical Trial Design in Cell and Gene Therapy
Next Generation Gene Therapy
Regulatory Landscape for Cell and Gene Therapies: Global Perspectives
Targeting Rare Genetic Diseases with Gene Therapy
In Vivo Gene Therapy: Current Approaches and Future Directions
Personalized Medicine and Cell Therapy: Customizing Treatments for Individuals
Ethics of Gene Therapy in Children and Vulnerable Populations
Ethical Implications of Using Gene Therapy for Non Lethal Conditions
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