LLY

1,127.49

-0.31%↓

JNJ

233.13

-1.8%↓

ABBV

220.76

-0.61%↓

UNH

409.07

-0.34%↓

MRK

114.02

-1.81%↓

LLY

1,127.49

-0.31%↓

JNJ

233.13

-1.8%↓

ABBV

220.76

-0.61%↓

UNH

409.07

-0.34%↓

MRK

114.02

-1.81%↓

LLY

1,127.49

-0.31%↓

JNJ

233.13

-1.8%↓

ABBV

220.76

-0.61%↓

UNH

409.07

-0.34%↓

MRK

114.02

-1.81%↓

LLY

1,127.49

-0.31%↓

JNJ

233.13

-1.8%↓

ABBV

220.76

-0.61%↓

UNH

409.07

-0.34%↓

MRK

114.02

-1.81%↓

LLY

1,127.49

-0.31%↓

JNJ

233.13

-1.8%↓

ABBV

220.76

-0.61%↓

UNH

409.07

-0.34%↓

MRK

114.02

-1.81%↓

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Ovid therapeutics Inc

Avatud

SektorTervishoid

2.33 0.43

Ülevaade

Aktsiahinna muutus

24h

Praegune

Min

2.22

Max

2.33

Põhinäitajad

By Trading Economics

Sissetulek

-27M

-17M

Aktsiakasum

-0.125

Kasumimarginaal

-2,366.017

Töötajad

23

EBITDA

-5.5M

-18M

Soovitused

By TipRanks

Soovitused

Tugev "osta" hinnang

12 kuu keskmine prognoos

+131.74% upside

Dividendid

By Acuity

Järgmine tulemuste avaldamine

12. aug 2026

Turustatistika

By TradingEconomics

Turukapital

-42M

440M

Eelmine avamishind

1.9

Eelmine sulgemishind

2.33

Uudiste sentiment

By Acuity

50%

50%

162 / 342 Pingereas Healthcare

Ovid therapeutics Inc Graafik

Mineviku tootlus ei ole usaldusväärne näitaja tulevaste tulemuste kohta.

Ettevõttest 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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