Cell and Gene Therapies
Cell and gene therapies are transforming treatment approaches for genetic disorders, cancers, and rare diseases. This discussion will highlight recent breakthroughs in gene-editing technologies, particularly CRISPR, and their potential to offer cures for conditions once considered untreatable. It will also examine the regulatory and ethical challenges associated with these pioneering therapies.
Sub-Sessions:
- CRISPR and Gene Editing Technologies
- Stem Cell Therapies
- Regulatory Landscape for Gene Therapies
- Ethical Considerations in Gene Editing
- Patient Access and Affordability