QURE ALERT: FDA Reportedly Accuses uniQure of Pushing "Distorted" and "Manipulated" Data For "Failed" AMT-130 Drug Amid Pending Securities Class Action - Hagens Berman
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Federal Officials Condemn uniQure in WSJ Report: "Company Lied"
On
According to the report, "[a] senior FDA official said in a call with reporters Thursday that the data from the testing of
Worse, the WSJ reported "[t]he official also said a
The next day, STAT reported "[w]hat started months ago as a scientific disagreement between the FDA and
The reports follow a series of devastating reports, beginning
The uniQure N.V. (QURE) Securities Class Action:
Class Period:
Lead Plaintiff Deadline:
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Summary of Allegations: The "Pivitol" Study Mirage
The complaint alleges that throughout the Class Period defendants misrepresented and failed to disclose that:
- The design of uniQure's Pivotal Study – including comparison of the Pivotal Study results to the ENROLL-HD external historical data set – was not fully approved by the
U.S. Food and Drug Administration ("FDA"); and - Defendants downplayed the likelihood that, despite purportedly highly successful results from the AMT-130 Pivotal Study, uniQure would have to delay its Biologics License Application ("BLA") timeline to perform additional studies to supplement its BLA submission.
The truth was allegedly revealed on
As a result, uniQure allegedly stated that "the timing of the BLA submission for AMT-130 is now unclear," but that uniQure "plans to urgently interact with the FDA to find a path forward for the timely accelerated approval of AMT-130."
On this news, the price of uniQure ordinary shares fell more than 49%.
"The core of our investigation is the potential delta between what uniQure told investors about its interactions with the FDA and the details revealed in the recent Type A meeting minutes," said
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