AI Summary Scores: Intraday / Swing / Long scores are synthesized from multi-factor analysis for each timeframe. They summarize current conditions discussed in the report and do not constitute trading recommendations.
Intraday Trend Score: A 0–100 composite from the Trend Explorer™ analytics engine used for ranking and comparison. It describes current conditions and is not a forecast.
Trend Status: A rules-based label (Bullish / Mixed / Bearish) derived from signal confluence (trend structure, momentum, and positioning). It indicates alignment, not expected return.
At close
$15.32
−$0.31 (−2.01%) Close
Pre-market$15.80
+$0.48 (+3.16%) 9:05 PM ET
Prev closePrevC$15.63
OpenOpen$15.75
Day highHigh$16.28
Day lowLow$15.32
VolumeVol17,838
Avg volAvgVol2,560,819
On chart
Interval
Intervals apply to 1D & 5D.
Intervals apply to 1D & 5D.
Scale: Linear
Overlays
Panels
Style
Scale: Linear
Presets
Tools
Tickers only (no ^ indexes). Add up to 5.
Mkt cap
$973.62M
P/E ratio
-3.49
FY Revenue
$15.75M
EPS
-4.39
Gross Margin
-20.18%
Sector
Healthcare
AI report sections
MIXED
QURE
uniQure N.V.
No AI report section text found yet for this symbol.
NASDAQ: QURE: Kessler Topaz Meltzer & Check, LLP Files a Securities Fraud Class Action Lawsuit Against uniQure N.V. (QURE)
A securities fraud class action lawsuit has been filed against uniQure N.V. (NASDAQ: QURE) for allegedly making material misstatements about its Huntington's disease gene therapy drug AMT-130 and the FDA approval timeline. The lawsuit covers investors who purchased shares between September 24 and October 31, 2025. On November 3, 2025, uniQure revealed the FDA no longer agrees that Phase I/II study data may be adequate for a BLA submission, causing the stock to plummet 49% from $67.69 to $34.29 per share.
The company is the subject of a securities fraud lawsuit alleging material misstatements about its lead drug candidate AMT-130 and FDA approval prospects. The stock experienced a severe 49% price decline following disclosure that the FDA no longer agrees the trial data is adequate for BLA submission, indicating significant setbacks in the company's clinical development and regulatory timeline.
NegativeGlobeNewswire Inc.• Rosen Law Firm
ROSEN, NATIONAL TRIAL LAWYERS, Encourages uniQure N.V. Investors to Secure Counsel Before Important Deadline in Securities Class Action - QURE
Rosen Law Firm is notifying investors who purchased uniQure N.V. ordinary shares between September 24, 2025 and October 31, 2025 of an April 13, 2026 lead plaintiff deadline in an ongoing securities class action. The lawsuit alleges that uniQure misrepresented and failed to disclose that the design of its Pivotal Study for its Huntington's Disease drug candidate was not fully FDA-approved, and that the company downplayed the likelihood of delays to its Biologics License Application timeline.
QUREsecurities class actionlead plaintiff deadlineFDA approvalBiologics License ApplicationHuntington's Diseaseinvestor compensationmisrepresentation
Sentiment note
The company is the subject of a securities class action lawsuit alleging material misrepresentations regarding FDA approval status of its Pivotal Study and downplaying of BLA timeline delays. These allegations suggest management failed to disclose material risks to investors, resulting in investor losses.
NegativeGlobeNewswire Inc.• Rosen Law Firm
ROSEN, A LEADING NATIONAL FIRM, Encourages uniQure N.V. Investors to Secure Counsel Before Important Deadline in Securities Class Action - QURE
Rosen Law Firm is encouraging investors who purchased uniQure N.V. (NASDAQ: QURE) shares between September 24, 2025 and October 31, 2025 to join a securities class action lawsuit. The lawsuit alleges that uniQure misrepresented and failed to disclose that the design of its Pivotal Study for its Huntington's Disease drug candidate was not fully FDA-approved, and that the company downplayed the likelihood of delays to its Biologics License Application timeline. The lead plaintiff deadline is April 13, 2026.
QUREsecurities class actionFDA approvalBiologics License ApplicationHuntington's Diseasemisrepresentationinvestor lawsuit
Sentiment note
The company is the subject of a securities class action lawsuit alleging material misrepresentations and omissions regarding FDA approval status of its Pivotal Study and BLA timeline delays. These allegations suggest potential regulatory setbacks and investor losses, which are negative indicators for the company's credibility and stock performance.
NegativeGlobeNewswire Inc.• Claimsfiler
uniQure Shareholder Alert: ClaimsFiler Reminds Investors With Losses In Excess Of $100,000 Of Lead Plaintiff Deadline In Class Action Lawsuit Against uniQure N.V. - QURE
uniQure N.V. faces a securities class action lawsuit for failing to disclose material information about its drug candidate AMT-130. The company previously represented high likelihood of FDA accelerated approval, but on November 3, 2025, disclosed the FDA no longer agrees the Phase I/II data is adequate for a BLA submission. The stock plummeted 49% from $67.69 to $34.29 on the news. Investors with losses exceeding $100,000 have until April 13, 2026 to file lead plaintiff applications.
QUREsecurities class actionFDA approvalmaterial information disclosurestock price declinelead plaintiff deadlineAMT-130BLA submission
Sentiment note
Company faces securities litigation for allegedly failing to disclose material information about FDA approval prospects for its lead drug candidate. Stock experienced a severe 49% price decline following disclosure of FDA's rejection of trial data adequacy, indicating significant investor losses and loss of confidence in the company's drug development program.
UNIQURE CLASS ACTION ALERT: Bragar Eagel & Squire, P.C. Encourages uniQure N.V. Stockholders with Large Losses to Contact the Firm
A class action lawsuit has been filed against uniQure N.V. for allegedly making materially false and misleading statements during September 24 - October 31, 2025. The complaint alleges the company misrepresented FDA approval of its Pivotal Study design and downplayed the likelihood of delays in its BLA submission timeline. Investors who suffered losses can contact the law firm by April 13, 2026 to be appointed as lead plaintiff.
The company is the subject of a class action lawsuit alleging material misrepresentations and omissions regarding its Pivotal Study FDA approval status and BLA timeline delays, indicating serious regulatory and operational concerns that resulted in investor losses.
uniQure N.V. Securities Fraud Class Action Result of FDA Approval Delay and 49% Stock Decline - Investors may Contact Lewis Kahn, Esq, at Kahn Swick & Foti, LLC
Kahn Swick & Foti, LLC has filed securities fraud class action lawsuits against uniQure N.V., Corcept Therapeutics, and BellRing Brands for allegedly failing to disclose material information to investors. uniQure's stock declined 49% after the FDA rejected data supporting its drug candidate AMT-130's accelerated approval. Similar FDA approval issues and inventory problems caused significant stock declines at the other companies. Investors have until April 13, 2026 to file lead plaintiff applications.
QUREBRBRCORTsecurities fraudclass action lawsuitFDA approvalstock declinematerial information disclosure
Sentiment note
Company faces securities fraud allegations for misrepresenting FDA approval likelihood for drug candidate AMT-130. Stock declined 49% after FDA rejected supporting data, causing substantial investor losses.
Corcept Therapeutics Incorporated Securities Fraud Class Action Result of FDA Approval Issues and 50% Stock Decline - Investors may Contact Lewis Kahn, Esq, at Kahn Swick & Foti, LLC
Kahn Swick & Foti, LLC announced multiple securities fraud class action lawsuits against pharmaceutical and consumer companies. Corcept Therapeutics faces allegations of failing to disclose material information about its relacorilant drug candidate, which received a Complete Response Letter from the FDA instead of approval, causing a 50.4% stock decline. Similar lawsuits were filed against uniQure N.V. for FDA approval delays (49% decline) and BellRing Brands for inventory issues (52% decline). Investors have until April 21, 2026 to file lead plaintiff applications.
CORTQUREBRBRsecurities fraudclass action lawsuitFDA approvalstock declinematerial information disclosure
Sentiment note
Company involved in securities fraud class action related to FDA approval delays, resulting in a 49% stock decline.
BellRing Brands, Inc. Securities Fraud Class Action Result of Inventory Issues and 52% Stock Decline - Investors may Contact Lewis Kahn, Esq, at Kahn Swick & Foti, LLC
Kahn Swick & Foti, LLC has filed securities fraud class action lawsuits against BellRing Brands, uniQure N.V., and Corcept Therapeutics for allegedly failing to disclose material information. BellRing's stock declined 52% following inventory and retailer supply issues, uniQure's stock fell 49% due to FDA approval delays, and Corcept's stock dropped 50% related to FDA approval issues. Investors have until March 23, 2026 to file lead plaintiff applications.
QURECORTBRBRsecurities fraudclass action lawsuitstock declinematerial information disclosureFDA approval
Sentiment note
Stock declined 49% following FDA approval delays. Securities fraud class action filed for alleged failure to disclose material information related to regulatory approval issues.
Bronstein, Gewirtz & Grossman LLC Urges uniQure N.V. Investors to Act: Class Action Filed Alleging Investor Harm
A class action lawsuit has been filed against uniQure N.V. alleging that company defendants made materially false and misleading statements regarding FDA approval of their Pivotal Study design and the likelihood of delays to their BLA timeline. The lawsuit covers investors who purchased uniQure securities between September 24, 2025 and October 31, 2025, with a lead plaintiff deadline of April 13, 2026.
The company is the subject of a securities fraud class action lawsuit alleging material misrepresentations and omissions regarding FDA approval of study design and BLA timeline delays, which directly harms investor interests and indicates serious corporate governance and disclosure failures.
NegativeGlobeNewswire Inc.• Rosen Law Firm
ROSEN, NATIONAL TRIAL LAWYERS, Encourages uniQure N.V. Investors to Secure Counsel Before Important Deadline in Securities Class Action - QURE
Rosen Law Firm is soliciting investors who purchased shares of uniQure N.V., Vistagen Therapeutics, Inc., and Lufax Holding Ltd during specified periods to join securities class action lawsuits. The uniQure lawsuit alleges the company misrepresented FDA approval of its Pivotal Study design and downplayed delays to its Biologics License Application timeline. The lead plaintiff deadline for uniQure is April 13, 2026.
QUREVTGNLUsecurities class actionFDA approvalBiologics License ApplicationHuntington's Diseaseinvestor losses
Sentiment note
The company is accused of misrepresenting FDA approval status of its Pivotal Study and failing to disclose likelihood of BLA submission delays, resulting in investor damages when true details emerged.
NegativeGlobeNewswire Inc.• The Schall Law Firm
QURE Investors Have Opportunity to Lead uniQure N.V. Securities Fraud Lawsuit with the Schall Law Firm
The Schall Law Firm is seeking investors who purchased uniQure N.V. (NASDAQ: QURE) securities between September 24, 2025, and October 31, 2025, for a class action lawsuit alleging securities fraud. The company allegedly made false and misleading statements regarding FDA approval for its Pivotal Study and misrepresented the timeline for its BLA submission, resulting in investor losses.
The company is the subject of a securities fraud lawsuit alleging false and misleading statements about FDA approval and BLA timeline, which caused investor losses. This represents significant legal and reputational risk.
NegativeBenzinga• Prnewswire
QURE Investors Have Opportunity to Lead uniQure N.V. Securities Fraud Lawsuit with the Schall Law Firm
The Schall Law Firm is seeking investors who purchased uniQure N.V. (NASDAQ: QURE) securities between September 24, 2025, and October 31, 2025, to join a class action lawsuit alleging securities fraud. The company allegedly made false and misleading statements regarding FDA approval for its Pivotal Study and misrepresented the likelihood of delays to its BLA timeline. Investors who suffered losses are encouraged to contact the firm before April 13, 2026.
The company is facing a securities fraud class action lawsuit for making false and misleading statements about FDA approval prospects and BLA timeline delays, resulting in investor losses and reputational damage.
News and sentiment labels describe article tone and are provided for research purposes only. They are not trading recommendations or forecasts.
Trade Ranks App
Trade Ranks, LLC is not a registered investment adviser or broker-dealer. All rankings and AI reports are for informational and educational purposes only and are not personalized advice. Investing involves risk. Policy Portal