3 Low-Beta Stocks to Minimize Portfolio Risk: LQDA, ET & PBF
Liquidia, Energy Transfer and PBF Energy offer low-beta exposure as oil-driven volatility rises, backed by growth, stable fees and refining demand.
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EU Clears AZN's Etcamah Combo for First-Line ER-Positive Breast Cancer
AstraZeneca secures EU approval for Etcamah in combination with a CDK4/6 inhibitor for first-line treatment of advanced ER-positive breast cancer patients.
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Liquidia vs. United Therapeutics: Which PAH Stock Is the Better Buy Now?
Liquidia's Yutrepia launch is fueling rapid growth, outperforming United Therapeutics on estimates and share gains despite a higher valuation.
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FDA Accepts BridgeBio's Filing for Rare Genetic Disease Drug
BBIO's FDA filing for encaleret in ADH1 has been accepted, moving the rare disease candidate closer to a decision expected by May 2027.
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PFE's Talzenna sNDA Gets FDA Priority Tag in Wider Prostate Cancer Use
Pfizer's Talzenna plus Xtandi combo wins FDA priority review for HRR gene-mutated metastatic castration-sensitive prostate cancer.
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Repligen to Expand Cell Therapy Capabilities With BioLife Buyout
RGEN's $1.5 billion BioLife acquisition aims to expand its cell therapy capabilities, adding biopreservation products and expected revenue and EPS benefits.
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Insider Decision: Stephen M Bloch Offloads $6.29M Worth Of Liquidia Stock
On July 22, a recent SEC filing unveiled that Stephen M Bloch, Board Member at Liquidia (NASDAQ:LQDA) made an insider sell.
What Happened: Bloch's decision to sell 78,596 shares of Liquidia was revealed in a Form 4read more...
Benzinga
Dr. Reddy's Q1 Earnings and Revenues Miss Estimates, Stock Down
RDY's fiscal Q1 earnings and revenues miss estimates as weaker North America generics sales hurt results, sending shares down 9%.
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GSK Lands FDA Approval for Nuvalent-Acquired Jideytro for NSCLC
GSK secures early FDA approval for Jideytro, its first lung cancer therapy, backed by strong ARROS-1 data, and strengthens its precision oncology portfolio.
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AGIO Shares Sink Nearly 7% After Scrapping the Tebapivat SCD Program
Agios drops after ending tebapivat development for SCD as phase II data confirmed PK activation but failed to show sufficient clinical differentiation.