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iShares Health Innovation Active ETF

33.80

+0.02710.08%

Post-market: 33.77-0.0271-0.08%16:10 EDT

Volume:222

Turnover:8K

Market Cap:13.52M

PE:- -

High:33.80

Open:33.77

Low:33.80

Close:33.77

52wk High:34.98

52wk Low:27.25

Shares:400.00K

Float Shares:400.00K

Volume Ratio:0.14

T/O Rate:0.06%

Dividend:0.08

Dividend Rate:0.24%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Yahong Meditech's APL-2501 Doses First Patient in Phase I Study for Advanced Solid Tumors

Hong Kong Stock Flash | JW (Cayman) Therapeutics (02126) Surges Over 20% Intraday as CAR-T Therapy Makes Historic Debut in Basic Medical Insurance Negotiations

Insight Molecular Diagnostics Revises Chronix Royalty Agreement Terms

Biogen Inc. Stock Outperforms Competitors on Strong Trading Day

Estee Lauder Cos. Cl a Stock Outperforms Competitors on Strong Trading Day

Moderna Inc. Stock Climbs 12.3%, Outperforms Peers

Nvidia Corp., Merck Share Gains Lead Dow's 425-Point Climb

J&J says Caplyta Phase 3 study in bipolar I met primary endpoint

Pharma Sector Doubles Down on AI to Slash Costs, Timelines

Avalyn Pharma announces published results from Phase 1 trials of AP02

InspireMD Announces Amendments to Certain Series J and Series K Warrants, Providing Potential Gross Proceeds of Up to $11 Million

Johnson & Johnson Says Phase 3 Trial Shows Caplyta Cuts Bipolar I Mania Symptoms by Week 3

J&J - Caplyta Demonstrates Statistically Significant Rapid Reduction in Manic Symptoms at Week 3

THOMSON REUTERS

Caplyta® (Lumateperone) Shows Significant and Rapid Improvement in Bipolar Mania in Pivotal Phase 3 Study

THOMSON REUTERS

J&J - Caplyta Well-Tolerated; Dry Mouth and Nausea Most Common Adverse Events

THOMSON REUTERS

LIVE Markets-Big Beauty Faces Growing Threat from AI, Smaller Rivals

Japan Health Ministry Approves Merck’s Keytruda QLEX for Subcutaneous Use Across Keytruda Indications

Merck’s Keytruda Qlex™ (Pembrolizumab and Berahyaluronidase Alfa-Pmph) Approved in Japan for Subcutaneous Administration for All Keytruda® (Pembrolizumab) Indications Approved in Japan

THOMSON REUTERS

Ultragenyx price target raised to $35 from $32 at Barclays

Jiangsu Hengrui Pharmaceuticals Secures Clinical Trial Approval for SHR-4595 Injection

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