$ALDX

Aldeyra Therapeutics, Inc.

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No SEC Form 4 filings for $ALDX in the last 30 days.

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EyeWorld Weekly, October 2, 2026

Rayner's RayOne Galaxy IOLs received FDA approval. Aldeyra plans to appeal FDA's rejection of reproxalap for dry eye disease. Sydnexis' SYD-101 for myopia will be reviewed at an FDA Advisory Committee meeting. Kodiak Sciences reported positive Phase 3 trial results for Zenkuda and KSI-501 in wet AMD. 4D Molecular Therapeutics began a Phase 3 trial for DME treatment with 4D-150. A study found a 16.1% increase in corneal transplants over 10 years, but supply-demand gap remains severe.

Rapid Dry Eye Relief With Investigational Reproxalap Drop

A pooled analysis of two trials found that reproxalap eye drops reduced dry eye symptoms more than a vehicle drop, with benefits seen in the first week. The most common side effect was irritation at the drop site. The study was funded by Aldeyra Therapeutics and published in Ophthalmology and Therapy.

ALDX sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 1 news story mentioning ALDX (Aldeyra Therapeutics, Inc.). Coverage has skewed bearish: 0 bullish, 0 neutral, and 1 bearish.

Recent ALDX coverage spans regulation, technology and corporate actions.

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AlphAI scores every news story that mentions ALDX with an AI model for sentiment and relevance, and aggregates insider trades from Aldeyra Therapeutics, Inc.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $ALDX

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$ALDXHighAI 8/10

EyeWorld Weekly, October 2, 2026

Rayner's RayOne Galaxy IOLs received FDA approval. Aldeyra plans to appeal FDA's rejection of reproxalap for dry eye disease. Sydnexis' SYD-101 for myopia will be reviewed at an FDA Advisory Committee meeting. Kodiak Sciences reported positive Phase 3 trial results for Zenkuda and KSI-501 in wet AMD. 4D Molecular Therapeutics began a Phase 3 trial for DME treatment with 4D-150. A study found a 16.1% increase in corneal transplants over 10 years, but supply-demand gap remains severe.

$ALDXHighAI 8/10

Aldeyra Therapeutics Stock Surges as It Files an FDA Dispute Resolution - Aldeyra Therapeutics (NASDAQ:AL

Aldeyra Therapeutics (ALDX) shares rose 13.79% after the company announced plans to submit a formal dispute resolution request to the FDA regarding its reproxalap program for dry eye disease. The FDA previously issued a Complete Response Letter citing insufficient evidence of efficacy. The move is seen as company-specific rather than sector-wide.

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Reproxalap for the Potential Treatment of Dry Eye Disease: Regulatory Update CONFERENCE CALL September 29, 2026 Nasdaq: ALDX

Aldeyra Therapeutics, Inc. (ALDX) filed an SEC Form 8-K — Other Events. Reproxalap for the Potential Treatment of Dry Eye Disease: Regulatory Update CONFERENCE CALL September 29, 2026 Nasdaq: ALDX © Aldeyra Therapeutics, Inc. 2026 Exhibit 99.1 Disclaimers and Forward-Looking Statements This presentation contains forward-looking statements within the

$ALDXLow

Aldeyra Therapeutics, Inc. (ALDX): Entry into a Material Definitive Agreement

Aldeyra Therapeutics, Inc. (ALDX) filed an SEC Form 8-K — Entry into a Material Definitive Agreement. Item 1.01. Entry into a Material Definitive Agreement. On July 28, 2026, Aldeyra Therapeutics, Inc. (“Aldeyra” or the “Company”) executed a lease agreement (the “Office Lease”) with Bradford Street, L.L.C. (“Bradford Street”) for approximately 4,067 square feet of office space lo

$ALDXLow

Aldeyra Therapeutics, Inc. (ALDX): Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers

Aldeyra Therapeutics, Inc. (ALDX) filed an SEC Form 8-K — Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers. 8-K false 0001341235 Massachusetts 0001341235 2026-06-09 2026-06-09 UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event report

$ALDXMed

[10-Q] Aldeyra Therapeutics, Inc. Quarterly Earnings Report

Aldeyra Therapeutics, Inc. (ALDX) has filed its quarterly earnings report (10-Q) for the period ended March 31, 2026, revealing a net loss of $3.5 million, a significant improvement from $9.9 million in the same period last year due to decreased research and development and general and administrative expenses. The company's cash and cash equivalents stood at $65.0 million, and it anticipates these funds will be sufficient to cover operating expenses and debt obligations into the second half of 2028. Aldeyra is highly reliant on the successful commercialization of reproxalap, currently awaiting potential FDA approval, and acknowledged risks associated with regulatory hurdles, intense competition, and the necessity of securing additional funding for future development and commercialization efforts.

$ALDXHigh

REMINDER: Aldeyra Therapeutics, Inc. Investors With Significant Losses Must Act By May 29, 2026

Kirby McInerney LLP reminds investors of Aldeyra Therapeutics, Inc. (NASDAQ: ALDX) about the May 29, 2026 deadline to become a lead plaintiff in a federal securities class action lawsuit. The lawsuit alleges that Aldeyra failed to disclose inconsistent results from clinical trials of its drug candidate, reproxalap, leading to a significant stock price drop following a Complete Response Letter from the FDA. Investors who purchased Aldeyra securities between November 3, 2023, and March 16, 2026, are encouraged to contact the firm to discuss their rights.

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