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Aptus Drawdown Managed Equity ETF

56.68

+0.39000.69%

Post-market: 56.680.00000.00%19:30 EDT

Volume:13.56K

Turnover:768.14K

Market Cap:311.27M

PE:- -

High:56.83

Open:56.71

Low:56.52

Close:56.29

52wk High:57.35

52wk Low:48.24

Shares:5.49M

Float Shares:5.49M

Volume Ratio:1.39

T/O Rate:0.25%

Dividend:0.20

Dividend Rate:0.36%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

ADM Energy Faces Extended AIM Trading Suspension Amid Reporting Delays

ADM Energy Secures Adjournment in HMRC Winding-Up Case as AIM Suspension Persists

Erasca Announces Multiple Presentations at the Upcoming 38th EORTC-NCI-AACR Symposium

AI Hardware Stocks Surge Despite Strong Jobs Report Weighing on Wall Street

Press Release: Anavex Life Sciences Reports Preliminary Second Quarter 2026 Financial Results and Provides Business Update

ADM Energy gains adjournment in HMRC winding-up case as tax claim is cut

Hedge Fund Manager Ackman Sees Meta and Amazon as Undervalued, Claims Broader Market Not Overpriced

ADM Energy Faces HMRC Winding-Up Petition as It Scrambles for Funding

AstraZeneca’s AZD1390 ADME Study Lays Groundwork for Future Oncology Upside

InnoCare Announce First Subject Dosed in Phase 1 Clinical Trial of ICP-054, a Novel Potentially Best-in-Class Oral IL-17AA/AF Inhibitor

Erasca Announces Positive Preliminary Phase 1 Dose Escalation Data for Potentially Best-in-Class Pan-RAS Molecular Glue ERAS-0015 in KRAS-Mutant Solid Tumors

Erasca to Host Conference Call and Webcast to Discuss Preliminary Phase 1 Dose Escalation Data for Potentially Best-in-Class Pan-RAS Molecular Glue ERAS-0015

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The strategy concentrates resources on. blarcamesine across three CNS indications: early Alzheimer's disease and. Rett syndrome, where the Company's clinical and regulatory foundation is. most advanced, and Fragile X, where FDA Orphan Drug Designation,supportive preclinical and biomarker data, and the absence of any. approved therapy may lead to a promising regulatory path with the FDA.Alzheimer's Disease Program-- At the end of March 2026, the Company opened an Investigational New Drug.  application for early Alzheimer's disease with the FDA. 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