Nusinersen Injection, the world’s first SMA (Spinal Muscular Atrophy) precision targeted therapy, was completed the intrathecal injection to the first SMA patients in China on Oct. 10, 2019, marking a new milestone of SMA treatment.
SMA is a rare genetic neuromuscular disease, with an incidence of about 1/6,000-1/10,000 in newborns. SMA is divided into SMA-I, II, III, and IV according to the onset age and motor milestone achieved. Most SMA-I infantile patients cannot survive to 2 years old if they are not treated. The disease did not have any therapy until the marketing of Nusinersen Injection. Therapeutic measures for SMA in China and worldwide were only limited to adjuvant therapies such as respiratory support, nutritional support, and orthopedics.
Nusinersen Injection (registered trade name: SPINRAZA in the U.S. and the EU) is developed by Biogen Idec Ltd and was first approved in the U.S. on Dec. 23, 2016, being the world’s first SMA precision targeted therapy. The drug has so far been approved in the EU, Brazil, Japan, South Korea, and Canada, etc. for treating SMA. Nusinersen Injection was officially approved by the National Medical Products Administration of China (NMPA) on Feb. 22, 2019, to treat 5q SMA and become the first SMA drug in China.
Nusinersen (Spinraza) is an antisense oligonucleotide that can alter SMN2 splicing and increase the production of full-length SMN protein, being a gene therapy drug. Nusinersen Injection can directly deliver the drug to the cerebrospinal fluid around the spinal cord through intrathecal injection, to improve the motor function, increase survival and change SMA progress. The drug won the "Best Biotechnology Product" in the 2018 International Prix Galien awarded in Nov. 2018.
Nusinersen Injection (Spinraza) is quite expensive in the U.S.: it is priced at USD125,000/injection and requires 6 injections in the first year, costing about USD750,000, and the cost for the second year is halved to USD375,000. The unit selling price of the drug is RMB697,000 in China, which has set a new record of pharmaceutical selling prices in China, and patients have to pay at their own expense. We look forward to that the SMA drug could be included in China’s national or local medical insurance drug catalog soon, to help SMA patients’ families solve the burden of treatment and make guaranteeing the drug access of rare disease patients become a reality.
Figure: Sales Data of Spinraza (source: Pharmcube, NextPharma)
Nusinersen Injection (Spinraza) has obtained the Orphan Drug Designation both in the U.S. and the EU. SMA was listed in the First List of Rare Diseases jointly issued by departments including the National Health Commission of China (NHC), etc. in May 2018. The entire approval cycle of Spinraza was less than 6 months (173 days) in China, and its approval date was also only 2 years and 2 months (794 days) from its first approval in the U.S. Such fast approval speed was thanks to China’s series of policies for rare diseases and overseas new drugs catering to clinical urgent needs:
In Dec. 2017, the former China Food and Drug Administration issued the Opinions of the China Food and Drug Administration on Encouraging Priority Review and Approval for Drug Innovation, clearly proposing to add rare disease drugs to the scope of priority review.
In May 2018, the NMPA and NHC issued the Announcement on Matters concerning the Optimization of Drug Registration Review and Approval, clearly proposing that for the pharmaceutical products already marketed overseas for prevention and treatment of diseases that are seriously life-threatening and have no effective treatment means, and rare diseases, if applicants for registration of these imported pharmaceutical products have confirmed after study there is no any ethnic difference, they can directly apply for drug marketing registration via submitting the clinical trial data obtained overseas.
The executive meeting of the State Council of China on June 20, 2018 proposed to orderly accelerate the marketing approval of overseas marketed new drugs in China and simplify the marketing requirements for some pharmaceutical products that treat ...
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