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Goldman Sachs Future Health Care Equity ETF

36.52

0.0000

Volume:10

Turnover:365.61

Market Cap:19.17M

PE:- -

High:36.52

Open:36.52

Low:36.52

Close:36.52

52wk High:38.66

52wk Low:31.32

Shares:525.00K

Float Shares:525.00K

Volume Ratio:0.03

T/O Rate:0.00%

Dividend:0.11

Dividend Rate:0.31%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Huihe Medical's STAR Market IPO Application Terminated; Company Focuses on Innovative Medical Devices in Panvascular Intervention

UnitedHealth Adds Jodee Kozlak as Chief Administrative Officer Effective Sept. 28, 2026

UnitedHealth Group Announces Addition to Leadership Team

THOMSON REUTERS

UnitedHealth - Appoints Jodee Kozlak as Chief Administrative Officer Effective Sept. 28, 2026

THOMSON REUTERS

Lifetech Scientific's SureCham Aortic Arch Single-Branch Stent Graft System Enters Special Review Pathway for Innovative Medical Devices

Milestone Pharmaceuticals Enrolls First Canadian Study Participant in ReVeRA-301 Phase 3 Pivotal Trial Evaluating Etripamil Nasal Spray for AFib-RVR

Merck's Drug for Diabetes-Related Eye Disease Meets Trial Goal

Eli Lilly Gets FDA OK for Onswik Once-Weekly Insulin Injection

Merck Says Remigromig Meets Primary Endpoint in Pivotal Brunello Trial for Diabetic Macular Edema

Eli Lilly - Onswik Kwikpen to be Available in U.S. in 500 Units/Ml and 1,000 Units/Ml Concentrations

THOMSON REUTERS

U.S. Food and Drug Administration (FDA) Approves Lilly's Onswik™ (Insulin Efsitora Alfa-Gobe), a Once-Weekly Basal Insulin Injection Treatment for Adults Living with Type 2 Diabetes

THOMSON REUTERS

Merck & Co - Higher Rates of Pdr, Vitreous Hemorrhage, and Discontinuations with Remigromig

THOMSON REUTERS

Merck’s Remigromig, a Tri-Specific Agonist of the Wingless-Related Integration Site (Wnt) Pathway, Met Primary Endpoint in the Pivotal Phase 2B/3 Brunello Study of Adults with Diabetic Macular Edema

THOMSON REUTERS

Merck & Co Inc: Both Doses of Remigromig were Generally Well Tolerated

THOMSON REUTERS

Merck & Co - Both Remigromig Doses Show Non-Inferiority to Ranibizumab at 52 Weeks

THOMSON REUTERS

MediciNova completes LPLV in Phase 2b/3 clinical trial evaluating MN-166

MediciNova Announces Completion of Last Patient, Last Visit in the Double-Blind Portion of the Phase 2b/3 COMBAT-ALS Trial of MN-166 (Ibudilast)

Bioperfectus Secures Two Medical Device Registration Certificates

Maccura Biotechnology Secures Three Medical Device Registration Certificates

RBC Capital Sticks to Their Buy Rating for Eli Lilly & Co (LLY)

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