LLY

1,107.1

+0.49%↑

JNJ

240.14

+2.2%↑

ABBV

234.01

-0.14%↓

UNH

402.54

-0.87%↓

MRK

119.77

+1.35%↑

LLY

1,107.1

+0.49%↑

JNJ

240.14

+2.2%↑

ABBV

234.01

-0.14%↓

UNH

402.54

-0.87%↓

MRK

119.77

+1.35%↑

LLY

1,107.1

+0.49%↑

JNJ

240.14

+2.2%↑

ABBV

234.01

-0.14%↓

UNH

402.54

-0.87%↓

MRK

119.77

+1.35%↑

LLY

1,107.1

+0.49%↑

JNJ

240.14

+2.2%↑

ABBV

234.01

-0.14%↓

UNH

402.54

-0.87%↓

MRK

119.77

+1.35%↑

LLY

1,107.1

+0.49%↑

JNJ

240.14

+2.2%↑

ABBV

234.01

-0.14%↓

UNH

402.54

-0.87%↓

MRK

119.77

+1.35%↑

Search

Ovid therapeutics Inc

Open

SectorGezondheidszorg

2.42 7.08

Overzicht

Wijziging aandelenprijs

24u

Huidig

Min

2.26

Max

2.42

Belangrijke statistieken

By Trading Economics

Inkomsten

-27M

-17M

EPS

-0.125

Winstmarge

-2,366.017

Werknemers

23

EBITDA

-4.7M

-17M

Aanbevelingen

By TipRanks

Aanbevelingen

Strong Buy

12 Maanden Prognose

+136.89% upside

Dividenden

By Acuity

Volgende Winsten

12 aug 2026

Marktinformatie

By TradingEconomics

Marktkapitalisatie

-58M

425M

Vorige openingsprijs

-4.66

Vorige sluitingsprijs

2.42

Nieuwssentiment

By Acuity

50%

50%

143 / 342 Rangschikking in Healthcare

Ovid therapeutics Inc Grafiek

Eerdere prestaties zijn geen betrouwbare indicator voor toekomstige resultaten.

Over Ovid therapeutics Inc

Ovid Therapeutics Inc., 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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