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Pfizer (NYSE:PFE) Advances Oncology Portfolio with PADCEV + Keytruda Regimen

Pfizer Inc. (NYSE:PFE) and Astellas Pharma Inc. announced that the U.S.Food and Drug Administrationhas granted approval for PADCEV (enfortumab vedotin-ejfv) in combination with Merck’s Keytruda (pembrolizumab) or Keytruda QLEX. The therapy is now cleared for perioperative use in adults with muscle-invasive bladder cancer (MIBC) …

Team Kalkine | 24 November 2025

Gilead Sciences (NASDAQ:GILD) Finalizes Acquisition of TREX1 Program from Sprint Bioscience

Gilead Sciences (NASDAQ:GILD) has completed the acquisition of the TREX1 cancer program from Sprint Bioscience AB. The agreement includes an upfront payment of USD 14 million and future potential milestone payments that could reach as high as USD 400 million.

Team Kalkine | 24 November 2025

Veeva Systems (NYSE:VEEV) Reports 16% Q3 Revenue Growth as Cloud Demand Expands

Veeva Systems (NYSE:VEEV) reported a meaningful revenue increase for its fiscal third quarter ended October 31, 2025, supported by steady demand for its cloud-based solutions tailored to the life sciences sector. Totalrevenuerose 16%year-over-yearto USD 811.2 million, compared with USD 699.2 million in Q3 FY25. …

Team Kalkine | 21 November 2025

Crinetics (NASDAQ:CRNX) Begins Pivotal Trial Evaluating Paltusotine in Carcinoid Syndrome

Crinetics Pharmaceuticals Inc. (NASDAQ:CRNX) has initiated its Phase 3 CAREFNDR clinical trial evaluating paltusotine in adults with carcinoid syndrome, marking a major step toward expanding the therapeutic reach of its flagship drug. Carcinoid syndrome affects roughly 20 percent of people with neuroendocrine tumors, most …

Team Kalkine | 21 November 2025

SynCardia Systems (NASDAQ:PMI) Reaches Milestone with First Implantations of Emperor Artificial Heart

SynCardia Systems, LLC, a subsidiary of Picard Medical Inc. (NASDAQ:PMI), has reached a defining moment in the advancement of artificial organ technology. The company confirmed the first successful in vivo implantations of its fully implantable Emperor Total Artificial Heart, marking a pivotal milestone in …

Team Kalkine | 21 November 2025

Regeneron (NASDAQ:REGN) EYLEA HD Gains FDA Nod for RVO; Enhanced Dosing Flexibility

Regeneron Pharmaceuticals, Inc. (NASDAQ:REGN) announced that the U.S.Food and Drug Administrationhas approved EYLEA HD (aflibercept injection 8 mg) for adult patients with macular edema following retinal vein occlusion. This approval adds a monthly (every four-week) dosing option across all previously approved indications, including wet …

Team Kalkine | 20 November 2025

Amgen (NASDAQ:AMGN) Secures FDA Clearance for IMDELLTRA After Phase 3 Success

Amgen (NASDAQ:AMGN) has received full approval from the U.S.Food and Drug Administrationfor IMDELLTRA (tarlatamab-dlle), a targeted therapy for adults with extensive-stage small cell lung cancer (ES-SCLC) whose disease has progressed on or after platinum-based chemotherapy. This decision upgrades IMDELLTRA’s initial accelerated approval, marking a …

Team Kalkine | 20 November 2025

Gilead (Nasdaq:GILD) Lenacapavir Arrives in Eswatini and Zambia in Major HIV Prevention Milestone

Gilead Sciences, Inc. (Nasdaq:GILD) has taken a crucial step in global HIV prevention with the first deliveries of its twice-yearly injectable PrEP medicine, lenacapavir, to Eswatini and Zambia. These shipments signify an important moment for communities in sub-Saharan Africa, a region that accounts for …

Team Kalkine | 19 November 2025

Zymeworks (Nasdaq:ZYME) Strategic Initiative Targets Expansion of Revenue-Generating Healthcare Assets

Zymeworks Inc. (Nasdaq:ZYME) has launched a strategic initiative designed to maximize long-term value from its growing roster of licensed biotherapeutics and healthcare assets. This decision follows encouraging developments across key programs, including positive topline data from the pivotal Phase 3 HERIZON-GEA-01 trial for Ziihera …

Team Kalkine | 19 November 2025

Arrowhead Pharmaceuticals (NASDAQ:ARWR) Achieves First FDA Nod with REDEMPLO Therapy

Arrowhead Pharmaceuticals Inc. (NASDAQ:ARWR) has achieved a major regulatory milestone as the U.S.Food and Drug Administration approvedREDEMPLO (plozasiran) for the treatment of adult patients with familial chylomicronemia syndrome. This marks the company’s first FDA-approved medicine and represents a pivotal step in its evolution from …

Team Kalkine | 19 November 2025