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BIRSA 101: India's 1st Indigenous CRISPR-Based Gene Therapy for Sickle Cell Disease
CSIR-IGIB’s CRISPR Gene Therapy Breakthrough for Sickle Cell Disease in India. India has launched its first indigenous CRISPR-based gene therapy for Sickle Cell Disease (SCD) . The therapy is named BIRSA 101 . The therapy is dedicated to Bhagwan Birsa Munda , a renowned tribal freedom fighter. BIRSA 101 has been developed by the CSIR–Institute of Genomics and Integrative Biology (IGIB) . About Gene Therapy Gene therapy is a medical technique that uses genes to treat, preve
Nov 212 min read
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