The Cost of Orphan Drugs
Karanveer Singh has Duchenne’s Muscular Dystrophy (DMD). His family has discovered an experimental therapy that skips the missing exon in the DMD gene, allowing dystrophin production. Despite bureaucratic obstacles, the Central Licensing Authority permitted a clinical trial across India. If successful, the treatment, developed by the Dystrophy Annihilation Research Trust (DART), will be available at a fraction of the cost of Western alternatives, offering hope to thousands of families.