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Aldeyra Therapeutics

1.77

-0.0700-3.80%

Post-market: 1.770.0003+0.02%19:35 EDT

Volume:2.61M

Turnover:4.66M

Market Cap:106.49M

PE:-3.14

High:1.84

Open:1.81

Low:1.76

Close:1.84

52wk High:6.73

52wk Low:1.07

Shares:60.16M

Float Shares:48.48M

Volume Ratio:0.40

T/O Rate:5.38%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-0.5636

EPS(LYR):-0.5636

ROE:-58.73%

ROA:-24.95%

PB:2.41

PE(LYR):-3.14

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Overview Company News Filings

Insider Makes Bold Move on Aldeyra Therapeutics Stock

Aldeyra Therapeutics Principal Financial Officer Michael Alfieri acquires USD 7,100 of common shares

What's Going On With Aldeyra Therapeutics Stock On Thursday?

Benzinga_recent_news

Levi & Korsinsky probes Aldeyra Therapeutics over potential securities fraud claims

Aldeyra Therapeutics Cut to Neutral From Buy by HC Wainwright & Co.

HC Wainwright Downgrades Aldeyra Therapeutics to Neutral From Buy, Adjusts PT to $2 From $10

MT Newswires Live

Aldeyra downgraded to Neutral from Buy at H.C. Wainwright

U.S. RESEARCH ROUNDUP-Factset, Lensar, Starbucks

BUZZ-U.S. STOCKS ON THE MOVE -Steel Dynamics, Aldeyra, Cencora

Aldeyra Therapeutics Shares Hit Record Low After US FDA Declines to Approve Eye Disorder Drug, Last Down 70%

THOMSON REUTERS

Aldeyra Therapeutics Shares Fall as Drug Rejected by Regulator on Efficacy Concerns

FDA issues Aldeyra CRL saying reproxalap NDA failed to demonstrate efficacy

How Did the FDA Shatter Investor Confidence In Aldeyra Therapeutics Stock (ALDX) Today?

Aldeyra Therapeutics Shares Down 73% Premarket After US FDA Declines to Approve Eye Disorder Drug

THOMSON REUTERS

FDA issues complete response letter for Aldeyra’s reproxalap dry eye NDA

Aldeyra Therapeutics Inc - No Safety or Manufacturing Concerns Identified in Reproxalap Nda Review

THOMSON REUTERS

Aldeyra Therapeutics Inc - FDA States Reproxalap Nda Failed to Demonstrate Efficacy for Dry Eye Disease

THOMSON REUTERS

Aldeyra Therapeutics Receives Complete Response Letter From the U.S. Food and Drug Administration for the Reproxalap New Drug Application for the Treatment of Signs and Symptoms of Dry Eye Disease

THOMSON REUTERS

Aldeyra Therapeutics Inc - to Request Type a Meeting With FDA Within 30 Days per Pdufa Goals

THOMSON REUTERS

Aldeyra Therapeutics Inc - FDA Recommends Exploring Trial Failures; No Additional Trials Requested for Reproxalap

THOMSON REUTERS

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While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 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The agency also said the data doesn't support the drug's effectiveness, though it raised no safety or manufacturing concerns.Aldeyra noted that the FDA didn't recommend conducting additional trials or request submission of additional confirmatory evidence.In the meantime, Aldeyra won't pursue any new clinical trials, but said it plans to meet with the FDA to understand th","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":"Aldeyra Therapeutics Shares Fall as Drug Rejected by Regulator on Efficacy Concerns","news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","ALDX"],"gpt_icon":0},{"id":"2620695420","title":"FDA issues Aldeyra CRL 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The FDA also said inconsistency of study results raised concerns about the reliability and meaningfulness of positive findings, and that the totality of evidence from completed clinical trials did not support effectiveness. Aldeyra reported cash, cash equivalents, and marketable securities of USD 70 million as of Dec. 31, 2025, and said it expects this to support operations into 2028.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 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