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Spark's blindness gene therapy reviewed by U.S. FDA
2017年10月10日 / 下午12点30分 / 10 天内

Spark's blindness gene therapy reviewed by U.S. FDA

Oct 10 (Reuters) - Spark Therapeutics Inc’s experimental gene therapy for a rare inherited form of blindness is effective, though it is unclear whether the benefit lasts over time, according to a preliminary review by the U.S. Food and Drug Administration.

The therapy, Luxturna, or voretigene neparvovec, would be the first ever gene therapy for an inherited disease to be approved in the United States.

The FDA’s review, posted on Tuesday on the agency’s website, comes two days ahead of a meeting of outside advisors who will discuss the treatment and recommend whether it should be approved.

Reporting by Toni Clarke in Washington

我们的标准:汤森路透“信任原则”
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