India Launches BIRSA 101: A Game-Changer in Sickle Cell Disease Treatment

Context

India has unveiled its first home-grown CRISPR-based gene therapy for Sickle Cell Disease (SCD), named BIRSA 101, marking a breakthrough in accessible and affordable genomic medicine.


About BIRSA 101 Gene Therapy

What is It?

BIRSA 101 is India’s first indigenously developed CRISPR gene-editing therapy aimed at curing Sickle Cell Disease (SCD)—a serious hereditary blood disorder that disproportionately affects tribal communities.

  • Developed by: CSIR–Institute of Genomics & Integrative Biology (IGIB)
  • In partnership with: Serum Institute of India (SIIPL)
  • Named after: Birsa Munda, on his 150th birth anniversary

Objectives

  • Contribute to India’s goal of becoming Sickle Cell–Free by 2047
  • Provide a low-cost indigenous alternative to prohibitively expensive global therapies
  • Strengthen India’s Atmanirbhar Bharat vision in advanced healthcare

How It Works

  • Utilises CRISPR as precise genetic surgery to correct the gene mutation responsible for SCD
  • Restores the ability of the body to produce normal haemoglobin
  • Edited stem cells are reinfused into the patient, enabling a potential one-time, lifelong cure

Key Features

  • Built on IGIB’s fully indigenous enFnCas9 gene-editing platform
  • Offers a significantly more affordable option than global therapies
  • Backed by a strong public–private partnership ensuring scalability and regulatory readiness
  • Supported by a new advanced translational research facility at CSIR-IGIB

Significance

  • Positions India as a global leader in next-generation gene therapies
  • Offers hope to millions in tribal communities heavily affected by SCD
  • Demonstrates India’s ability to deliver cutting-edge treatments at world-leading affordability

Conclusion

BIRSA 101 represents a transformative step in India’s healthcare innovation—combining scientific excellence, affordability, and social equity. By making gene therapy accessible to vulnerable populations, it strengthens India’s path toward eliminating Sickle Cell Disease and showcases the nation’s growing leadership in advanced genomic medicine.

Source : PIB

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