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iShares Health Innovation Active ETF

34.41
-0.1816-0.53%
Volume:1K
Turnover:46.45K
Market Cap:13.76M
PE:- -
High:34.41
Open:34.24
Low:34.24
Close:34.59
52wk High:34.79
52wk Low:25.79
Shares:400.00K
Float Shares:400.00K
Volume Ratio:0.36
T/O Rate:0.34%
Dividend:0.08
Dividend Rate:0.24%
ROE:--
ROA:--
PB:--
PE(LYR):- -

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Analysts Offer Insights on Healthcare Companies: GE Healthcare Technologies Inc (GEHC), Biogen (BIIB) and BeOne Medicines (ONC)

TIPRANKS
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8 mins ago

Merck price target raised to $180 from $155 at Wolfe Research

TIPRANKS
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52 mins ago

Merck (MRK) Stock May Be 35% Undervalued After Cancer Vaccine Data

Simply Wall St.
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11 hours ago

US FDA Expands Approval for J&J's Drug for Rare Blood Disorder

Reuters
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12 hours ago

FDA Approves J&J Imaavy for Warm Autoimmune Hemolytic Anemia Treatment

Reuters
·
12 hours ago

FDA Approves Imaavy® as First-Ever Treatment for Warm Autoimmune Hemolytic Anemia (Waiha), Representing a Landmark Advancement for Patients

THOMSON REUTERS
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12 hours ago

Moderna Inc. Stock Slides 4.3%, Underperforms Peers

Dow Jones
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14 hours ago

Lakefront Biotherapeutics Wins FDA Orphan Drug Status for Gamgertamig in Pemphigus

Reuters
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14 hours ago

Syngenis banks R&D refund to fuel biotech build-out

The West Australian
·
Yesterday

Moderna is Betting Big on Its Cancer Vaccine. This is What Wall Street Wants to See.

Dow Jones
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Yesterday

Renalytix Discloses Director’s Link to Trellus Administration as KidneyIntelX Rollout Advances

TIPRANKS
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Yesterday

Biogen, Eisai's LEQEMBI IQLIK Now Available in US for Early Alzheimer's Disease

MT Newswires Live
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Yesterday

Eisai, Biogen announces once weekly lecanemab-irmb availability in the U.S.

TIPRANKS
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Yesterday

Eisai Co., Ltd.: Leqembi Iqlik (Lecanemab-Irmb) Autoinjector for Initiation of Therapy NOW Available in U.S. for Early Alzheimer's Disease

THOMSON REUTERS
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Yesterday

CF PHARMTECH (02652) Secures Expanded Clinical Trial Approval for ICF001 Across Additional Indications

Stock News
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Yesterday

Barclays Raises Moderna PT on 'transformative' Melanoma Vaccine Potential

Reuters
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Yesterday

EU Commission Approves Gilead Trodelvy-Keytruda Combo for First-Line PD-L1+ Metastatic TNBC

Reuters
·
Yesterday

Gilead - EU Grants Marketing Authorization for Trodelvy with Keytruda in First-Line Pd-L1-Positive Metastatic Tnbc

THOMSON REUTERS
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Yesterday

European Commission Expands Role of Gilead’s Trodelvy® in First-Line Metastatic Triple-Negative Breast Cancer Across Pd-L1 Status

THOMSON REUTERS
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Yesterday

BAO PHARMA-B (02659) Receives US FDA Clearance for KJ015 Injection Clinical Trial Application

Stock News
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Yesterday