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Aldeyra Therapeutics

4.72
-0.0700-1.46%
Volume:762.00K
Turnover:3.62M
Market Cap:283.97M
PE:-6.55
High:4.84
Open:4.81
Low:4.68
Close:4.79
52wk High:7.20
52wk Low:1.14
Shares:60.16M
Float Shares:48.48M
Volume Ratio:0.91
T/O Rate:1.57%
Dividend:- -
Dividend Rate:- -
EPS(TTM):-0.7210
EPS(LYR):-0.9389
ROE:-64.31%
ROA:-28.94%
PB:5.77
PE(LYR):-5.03

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Aldeyra Therapeutics Inc - No Approved Treatment for Primary Vitreoretinal Lymphoma in EU

THOMSON REUTERS
·
Aug 28

Aldeyra Therapeutics Receives Orphan Designation From the European Medicines Agency for Adx-2191 for the Treatment of Primary Large B-Cell Lymphomas of Immune-Privileged Sites, Including Primary Vitreoretinal Lymphoma

THOMSON REUTERS
·
Aug 28

Aldeyra Therapeutics Receives FDA Fast Track Designation for ADX-2191 in Treating Retinitis Pigmentosa

Reuters
·
Aug 19

Aldeyra Therapeutics Inc - Phase 2/3 Trial of Adx-2191 Expected to Start in 2025

THOMSON REUTERS
·
Aug 19

Aldeyra Therapeutics Receives Fast Track Designation for Adx‑2191 for the Treatment of Retinitis Pigmentosa

THOMSON REUTERS
·
Aug 19

Michael Alfieri, Principal Financial Officer, Reports Acquisition of Common Shares of Aldeyra Therapeutics Inc

Reuters
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Aug 16

Stephen Machatha, Chief Development Officer, Reports Disposal of Aldeyra Therapeutics Inc. Common Shares

Reuters
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Aug 14

Aldeyra Therapeutics Inc expected to post a loss of 25 cents a share - Earnings Preview

Reuters
·
Aug 09

Aldeyra Therapeutics Unveils Innovative Therapies for Immune-Mediated and Metabolic Diseases in Latest Presentation

Reuters
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Aug 05

Aldeyra Therapeutics Inc expected to post a loss of 24 cents a share - Earnings Preview

Reuters
·
Jul 29

Aldeyra Therapeutics Secures Orphan Designation from European Medicines Agency for ADX-2191 to Treat Retinitis Pigmentosa

Reuters
·
Jul 24

Aldeyra Therapeutics Inc - Phase 2/3 Trial of Adx-2191 Expected in 2025

THOMSON REUTERS
·
Jul 24

Aldeyra Therapeutics Receives Orphan Designation From the European Medicines Agency for Adx-2191 for the Treatment of Inherited Retinal Dystrophies Including Retinitis Pigmentosa

THOMSON REUTERS
·
Jul 24

Aldeyra Therapeutics Announces FDA Acceptance of Reproxalap NDA for Dry Eye Disease with PDUFA Target Date Set for December 2025

Reuters
·
Jul 17

BRIEF-Aldeyra Therapeutics Receives Special Protocol Assessment Agreement Letter From The U.S. Food And Drug Administration For Adx-2191

Reuters
·
Jun 26

Aldeyra Therapeutics Resubmits New Drug Application for Reproxalap to FDA for Dry Eye Disease Treatment

Reuters
·
Jun 17

Aldeyra Therapeutics Inc. Concluded Annual Stockholders Meeting

Reuters
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Jun 12

Aldeyra Therapeutics to Participate in the Jefferies Global Healthcare Conference 2025

Reuters
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May 29

CORRECTED-US FDA approves Alcon's new dry-eye drug (May 28)

Reuters
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May 29

Aldeyra Therapeutics Price Target Maintained With a $10.00/Share by HC Wainwright & Co.

Dow Jones
·
May 19