HYDERABAD: A three-year-old Hyderabad boy with a rare genetic disorder was on Thursday administered a Rs 16-crore drugтАФsaid to be the worldтАЩs most expensive single-dose intravenous injection тАФas doctors attempted to cure his spinal muscular atrophy (SMA) type 1 condition that affects one in 8,000 children. Ayaansh Gupta got a shot of the US-manufactured drug Zolgensma, thanks to 62,450 people contributing Rs 14.84 crore through a crowdfunding site. The remaining Rs 1.2 crore came from an international crowdfunding initiative and his family
The Union government waived import duty of Rs 6 crore, without which the drug would have cost Rs 22 crore.
Children suffering from SMA type 1 rarely make it beyond two years of age without medical intervention. тАЬSMA is a progressive neuromuscular disease caused due to a defect in the SMN1 gene. Affected children show muscle weakness, involving upper and lower limbs initially, but overtime develop breathing and swallowing difficulty,тАЭ said Dr Ramesh Konanki, paediatric neurologist at Rainbow ChildrenтАЩs Hospital.
тАЬZolgensma is the single-dose intravenous injection of gene therapy, in which the defective SMN1 gene is replaced through adenoviral vector. Ayaansh is doing fine and will be under observation for a day.тАЭ
AyaanshтАЩs case had caught the attention of Bollywood celebrities and cricketers, with many of them donating to the fund and spreading the word. тАЬIt is heartening to witness the power of crowdfunding. A large number of donors came together to support Ayaansh GuptaтАЩs family in their journey of saving their child. The single highest donation received on the crowdfunding campaign is Rs 56 lakh and $7,000. We are super ecstatic at the moment,тАЭ said Piyush Jain, co-founder and CEO, ImpactGuru.com.
The Union government waived import duty of Rs 6 crore, without which the drug would have cost Rs 22 crore.
Children suffering from SMA type 1 rarely make it beyond two years of age without medical intervention. тАЬSMA is a progressive neuromuscular disease caused due to a defect in the SMN1 gene. Affected children show muscle weakness, involving upper and lower limbs initially, but overtime develop breathing and swallowing difficulty,тАЭ said Dr Ramesh Konanki, paediatric neurologist at Rainbow ChildrenтАЩs Hospital.
тАЬZolgensma is the single-dose intravenous injection of gene therapy, in which the defective SMN1 gene is replaced through adenoviral vector. Ayaansh is doing fine and will be under observation for a day.тАЭ
AyaanshтАЩs case had caught the attention of Bollywood celebrities and cricketers, with many of them donating to the fund and spreading the word. тАЬIt is heartening to witness the power of crowdfunding. A large number of donors came together to support Ayaansh GuptaтАЩs family in their journey of saving their child. The single highest donation received on the crowdfunding campaign is Rs 56 lakh and $7,000. We are super ecstatic at the moment,тАЭ said Piyush Jain, co-founder and CEO, ImpactGuru.com.
