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NASDAQ:OVID

Ovid Therapeutics Q4 2023 Earnings Report

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$0.29 +0.00 (+0.11%)
As of 10:23 AM Eastern
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Ovid Therapeutics EPS Results

Actual EPS
-$0.22
Consensus EPS
-$0.17
Beat/Miss
Missed by -$0.05
One Year Ago EPS
N/A

Ovid Therapeutics Revenue Results

Actual Revenue
$0.14 million
Expected Revenue
$0.10 million
Beat/Miss
Beat by +$40.00 thousand
YoY Revenue Growth
N/A

Ovid Therapeutics Announcement Details

Quarter
Q4 2023
Time
N/A
Conference Call Date
Friday, March 8, 2024
Conference Call Time
7:00AM ET

Earnings Documents

Ovid Therapeutics Earnings Headlines

What is B. Riley's Estimate for OVID Q2 Earnings?
How I profit during chaos…
This Guy THRIVES on Chaos Wall Street legend Larry Benedict has thrived through every major market crash. In the first quarter of this year, in one of the most volatile markets in history, he used his time-tested strategy to go 12 for 12. That's a 100% win–rate — while the rest of the world panics.
Wedbush Decreases Earnings Estimates for Ovid Therapeutics
Research Analysts Offer Predictions for OVID Q3 Earnings
See More Ovid Therapeutics Headlines
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About Ovid Therapeutics

Ovid Therapeutics (NASDAQ:OVID), a biopharmaceutical company, engages in the development of impactful medicines for patients and families with epilepsies and seizure-related neurological disorders in the United States. The company is developing soticlestat, a novel cholesterol 24 hydroxylase inhibitor, which is in Phase 3 clinical trials for the potential treatment of patients with resistant epilepsies; OV329, a GABA aminotransferase inhibitor which is in Phase 1 clinical trials for the treatment of seizures associated with tuberous sclerosis complex and infantile spasms; and OV350, a small molecule direct activator of the KCC2 transporter, which is in Phase 1 clinical trials for treating epilepsies. It also develops OV815, that focuses on the mutations associated with KIF1A-associated neurological disorder (KAND); OV888 (GV101), a highly selective rock2 inhibitor which is in Phase 1 double-blind multiple-ascending dose trial; OV825, has advanced to potential candidate lead identification for the rare neurodevelopmental condition HNRNPH2 (Bain Syndrome); and OV882, a short hairpin RNA gene therapy for the treatment of Angelman syndrome. The company has license and collaboration agreements with Healx, AstraZeneca AB, H. Lundbeck A/S, Northwestern University, and Graviton, as well as Marinus Pharmaceuticals, Inc. The company was incorporated in 2014 and is headquartered in New York, New York.

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