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Goldman Sachs Future Health Care Equity ETF

36.49

-0.0328-0.09%

Post-market: 36.490.00000.00%16:10 EDT

Volume:129

Turnover:5K

Market Cap:19.16M

PE:- -

High:36.49

Open:36.49

Low:36.49

Close:36.52

52wk High:38.66

52wk Low:31.32

Shares:525.00K

Float Shares:525.00K

Volume Ratio:0.18

T/O Rate:0.02%

Dividend:0.11

Dividend Rate:0.31%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

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

Oura Files for Initial Public Offering on Nasdaq

MT Newswires Live

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

Smart Ring Maker Oura Eyes $15.6 Billion IPO Valuation in Fall Listings Demand Test

Oura - Eli Lilly Interested in Purchasing up to $100 Mln; Dragoneer up to $300 Mln in IPO - SEC Filing

THOMSON REUTERS

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

Novo Says Its Next-Gen Obesity Drug Tops Lilly Rival in Late-Stage Study

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

China-Singapore Suzhou Industrial Park Invests Up to RMB 20 Million in Medical Device and Biotech Fund

Citi Highlights Policy Boost for Innovative Drugs and Medical Devices, Names Key Sector Picks

Innovative Drug Sector Heats Up: Spotlight on Pure-Play R&D Developers

Analysts Offer Insights on Healthcare Companies: Merck & Company (MRK), Envista Holdings (NVST) and Ultragenyx Pharmaceutical (RARE)

Eli Lilly, Novo sued over risk of sudden vision loss, WSJ reports

Cue Biopharma announces Phase 2 trial of CUE-221 met primary endpoint

Cue Biopharma Announces Positive Topline Results from CUE-221 Phase 2 Study in Chronic Spontaneous Urticaria

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