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First Trust Nasdaq Pharmaceuticals ETF

40.77

+0.03500.09%

Post-market: 40.770.00000.00%19:30 EDT

Volume:139.50K

Turnover:5.68M

Market Cap:1.05B

PE:- -

High:40.94

Open:40.57

Low:40.35

Close:40.73

52wk High:43.52

52wk Low:28.77

Shares:25.65M

Float Shares:25.65M

Volume Ratio:2.26

T/O Rate:0.54%

Dividend:0.29

Dividend Rate:0.71%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Bristol-Myers' Protocol Changes Add Risk, Keep Admilparant on Track, UBS Says

MT Newswires Live

BMY Expands Real-World Cancer Data With New AUGTYRO Study in Korea

Lilly’s Clazakizumab Trial Pushes Cardiovascular Inflammation Strategy Forward

AbbVie Wraps Key Early Trial on ABBV-722 Drug Interaction, Supporting Pipeline Confidence

AbbVie’s Bretisilocin Study Completion Signals Quiet Progress in Early-Stage Pipeline

Spyre Gains After Merck's Drug Succeeds in Skin Disease Trial

Eli Lilly Reports 'Positive' Results From EloraTZP Trial

MT Newswires Live

Weight-Loss Drug Developers Line up to Tap Lucrative Market as Competition Heats Up

Adding Lilly's New Drug to Zepbound Helped People Lose up to 23% of Their Weight. but There were More Side Effects.

Eli Lilly Says EloraTZP Combo Delivered 'Substantial' Weight Loss, A1C Reduction in Phase 2b Trial

MT Newswires Live

Lilly says participants on EloraTZP lost up to average 23.3% of weight in study

Lilly's Eloratzp (Combination of Eloralintide and Tirzepatide) Delivered Greater Weight Loss and A1c Reduction VS. Tirzepatide 15 Mg in Adults with Obesity and Type 2 Diabetes

THOMSON REUTERS

Eli Lilly: Plans to Initiate Phase 3 Studies of Eloratzp Co-Formulation Product by 2026 End Using Optimized Escalation Schedule

THOMSON REUTERS

Eli Lilly: at 48 Weeks, All Combinations of Eloratzp Met Primary & Secondary Endpoints

THOMSON REUTERS

Experimental Lilly Combination Drug Tops Zepbound in Weight-Loss Trial

Eli Lilly: Participants Taking Eloratzp Lost up to Average of 54.1 Lbs (23.3%) VS. 34.4 Lbs (14.8%) with Tirzepatide 15 Mg

THOMSON REUTERS

Merck Says Experimental Skin Disease Drug Meets Main Goal in Mid-Stage Study

Major Drugmakers Turn to China for Licensing Deals

Merck Says Tulisokibart Hits Primary Endpoint in Phase 2b Hidradenitis Suppurativa Trial

Merck & Co - Study Meets Primary Endpoint Hiscr50 at Week 16 for High- and Medium-Dose Tulisokibart

THOMSON REUTERS

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