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Agency ‘not convinced’ UniQure Huntington’s therapy has benefit

UniQure has accused the agency of reversing its stance on AMT-130, but hopes to settle on the parameters of a new trial.

BusinessBy Catherine ChenMarch 3, 20262 min read

Last updated: March 18, 2026, 2:25 AM

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Agency ‘not convinced’ UniQure Huntington’s therapy has benefit

Company accuses agency of reversal but hopes to settle on parameters of a new trial

Adam Feuerstein, a senior writer and biotech columnist, is the author of Adam’s Biotech Scorecard, a subscriber-only newsletter about the crossroads of drug development, business, Wall Street, and biotechnology.

Adam Feuerstein is a senior writer and biotech columnist, reporting on the crossroads of drug development, business, Wall Street, and biotechnology. He is also a co-host of the weekly biotech podcast The Readout Loud and author of the newsletter Adam’s Biotech Scorecard. You can reach Adam on Signal at stataf.54.

The Food and Drug Administration has concluded that an experimental treatment for Huntington’s disease developed by UniQure was not providing benefit for patients based on existing clinical data, a senior FDA official told STAT, explaining the agency’s decision to block the company from submitting a marketing application.

Agency reviewers “are not convinced there’s any therapeutic benefit of the product,” the official said, speaking on condition of anonymity.

“If we felt there was any therapeutic benefit, we, of course, would approve it. But they’re not persuaded,” the official added.

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Catherine Chen

Financial Correspondent

Catherine Chen covers finance, Wall Street, and the global economy with a focus on business strategy. A former financial analyst turned journalist, she translates complex economic data into clear, actionable reporting. Her coverage spans Federal Reserve policy, cryptocurrency markets, and international trade.

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