India's Potential in Developing Gene Therapy for Thalassemia and Sickle Cell Disease
Dr. Gaurav Kharya

India has the capability to develop its own innovative gene therapy solutions for thalassemia and sickle cell disease

Date 20-Feb-2024 | India has the capability to develop its own innovative gene therapy solutions for thalassemia and sickle cell disease

Dr Gaurav Kharya, Founder & Director of Delhi-based startup Cellogen Therapeutics, is working intensively on developing indigenous CAR T cell therapy for blood cancers in India so that the cost of treatment can be brought down. Also working as a Clinical lead at the Centre for Bone Marrow Transplant and Cellular Therapy & Senior consultant- paediatric hematology, oncology and immunology, Apollo Hospitals, New Delhi, Dr Kharya spoke to BioSpectrum about how Cell and Gene therapy is the future of medicine.