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OVID | Ovid Therapeutics Inc.

IndexRUT P/E- EPS (ttm)-0.70 Insider Own2.50% Shs Outstand70.53M Perf Week-8.31%
Market Cap248.58M Forward P/E- EPS next Y-0.80 Insider Trans0.00% Shs Float55.92M Perf Month-4.71%
Income-49.20M PEG- EPS next Q-0.19 Inst Own53.20% Short Float / Ratio3.72% / 7.22 Perf Quarter-2.41%
Sales0.20M P/S1242.88 EPS this Y-143.70% Inst Trans2.32% Short Interest2.08M Perf Half Y46.77%
Book/sh1.57 P/B2.32 EPS next Y-5.30% ROA-32.80% Target Price5.67 Perf Year89.58%
Cash/sh1.41 P/C2.58 EPS next 5Y- ROE-38.90% 52W Range1.40 - 4.14 Perf YTD95.70%
Dividend- P/FCF- EPS past 5Y25.50% ROI-42.00% 52W High-12.05% Beta1.10
Dividend %- Quick Ratio10.10 Sales past 5Y- Gross Margin- 52W Low159.07% ATR0.24
Employees40 Current Ratio10.10 Sales Q/Q- Oper. Margin- RSI (14)48.76 Volatility7.45% 6.50%
OptionableYes Debt/Eq0.00 EPS Q/Q15.10% Profit Margin- Rel Volume0.38 Prev Close3.61
ShortableYes LT Debt/Eq0.00 EarningsAug 04 BMO Payout- Avg Volume288.29K Price3.64
Recom1.80 SMA20-1.27% SMA501.13% SMA20022.40% Volume108,683 Change0.83%
Date Action Analyst Rating Change Price Target Change
Apr-20-21Downgrade Cantor Fitzgerald Buy → Neutral $4
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Dec-02-20Downgrade Citigroup Buy → Neutral $10 → $4
Sep-04-19Initiated RBC Capital Mkts Outperform $12
Apr-20-18Initiated Ladenburg Thalmann Buy $27
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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, currently under preclinical stage, that focuses on the mutations associated with KIF1A-associated neurological disorder (KAND); OV825, currently under preclinical stage, which has advanced to potential candidate lead identification for the rare neurodevelopmental condition HNRNPH2 (Bain Syndrome); and OV882, currently under preclinical stage, 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, and Northwestern University, as well as Marinus Pharmaceuticals, Inc. The company was incorporated in 2014 and is headquartered in New York, New York.