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AbbVie Wins FDA Approval for Pediatric Skyrizi, First IL-23 for Kids
The U.S. Food and Drug Administration (FDA) approved AbbVie's Skyrizi (risankizumab-rzaa) for children aged 6 and older. This approval covers pediatric...
Sandoz Challenges Eli Lilly With Generic Mounjaro and Zepbound Filings
The FDA accepted two applications from Swiss drugmaker Sandoz for generic versions of Eli Lilly’s tirzepatide medications, Mounjaro and Zepbound. These...
Merck KGaA Buys Bio-Techne for $11.3 Billion, Expanding Research Tools
Merck KGaA will acquire U.S. biotech firm Bio-Techne for $11.3 billion. The all-cash offer provides $73 per share to Bio-Techne investors. This price...
🟢 IYH is trading 3% up today on defensive rotation and healthcare M&A activity
IYH is trading 3% up today as investors rotate toward defensive, non-tech sectors following recent pressure in technology and AI-related names. • A volatile...
Merck KGaA Buys Bio-Techne for $11.3 Billion, Expanding High-Growth Life Sciences
Merck KGaA entered a definitive agreement to acquire Bio-Techne Corp. for $73 per share in cash. The transaction represents a total enterprise value of...
Merck Gains EU Approval for Keytruda-Padcev, Cutting Bladder Cancer Death Risk 50%
Merck received European Commission approval for KEYTRUDA in combination with the antibody-drug conjugate Padcev. The regimen treats adult patients with...
REGENXBIO Clears FDA Hurdle for NAVSUNLI™, No New Trials Needed
REGENXBIO reached an agreement with the FDA on a path to resubmit its Biologics License Application (BLA) for NAVSUNLI™. This one-time gene therapy targets...
U.S. Probes German Drug Pricing, Threatening Tariffs Following Eli Lilly Investment Cuts
The U.S. government initiated a formal trade investigation into Germany’s proposed drug-pricing reforms under Section 301 of the Trade Act of 1974. This probe...
FDA Issues High-Risk Alert for Johnson & Johnson's Abiomed Heart Pump
The U.S. Food and Drug Administration (FDA) has issued an alert for a 'potentially high-risk' leakage issue with Abiomed's Impella heart pump introducer kits....
Merck Wins FDA Approval for CAPVAXIVE in At-Risk Children
Merck received FDA approval for an expanded indication of its CAPVAXIVE vaccine. The approval covers children and adolescents aged 2 through 17 with underlying...
uniQure Surges as FDA Eases Path for Huntington’s Gene Therapy
The FDA reversed its stance to allow uniQure to file for accelerated approval of AMT-130, a Huntington's disease gene therapy. The agency will accept...
Pfizer settles 5,000 lawsuits, resolving Depo-Provera brain tumor claims
Pfizer reached a settlement in principle to resolve more than 5,000 lawsuits involving its Depo-Provera birth control shot. A Monday court filing confirmed the...
Johnson & Johnson invests $1B in ACUVUE, strengthening domestic supply chains
Johnson & Johnson will invest over $1 billion to expand its Vision operations in Jacksonville, Florida. The capital will scale domestic manufacturing,...
Legend Biotech Reports 100% Response Rate for In Vivo CAR-T Therapy
Legend Biotech (NASDAQ: LEGN) released clinical proof-of-concept data for LB2501, an investigational in vivo CAR-T cell therapy. The company presented the...
Johnson & Johnson Myeloma Combo Slashes Progression Risk by 72%
Johnson & Johnson announced Phase 3 MonumenTAL-3 study results for its TALVEY (talquetamab-tgvs) and DARZALEX FASPRO combination. The trial evaluated the...
J&J Reports Positive IMAAVY Data, Eyeing First-Ever Rare Blood Disorder Treatment
Johnson & Johnson reported positive initial results from its Phase II/III ENERGY trial for IMAAVY (nipocalimab-aahu). The investigational treatment targets...
Takeda’s zasocitinib beats BMS’s Sotyktu, showing 2.5x higher skin clearance
Takeda reported positive topline results from the LATITUDE Atlas Phase 3 study. The oral TYK2 inhibitor zasocitinib proved statistically superior to Bristol...
Eli Lilly widens obesity lead, sending rival Novo Nordisk shares lower
Eli Lilly presented detailed trial data for its experimental obesity drug, retatrutide, at the American Diabetes Association (ADA) conference. The data...
GSK acquires Nuvalent for $10.6B, targeting blockbuster lung cancer drugs
GSK signed a definitive agreement to acquire Nuvalent for $10.6 billion. The transaction secures a portfolio of next-generation precision cancer therapies and...
Eli Lilly surges, fueled by 30% weight loss for retatrutide
Eli Lilly released late-stage clinical trial data for its next-generation weight-loss drug, retatrutide. The drug led to a 30.3% average reduction in body...