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pharmaceuticals: Archive

Zacks Equity Research

NVS Ups Sales Projections as Key Drugs and Collaborations Fuel Growth

Novartis boosts long-term sales forecasts as blockbuster drugs like Kisqali and Scemblix drive strong momentum across its portfolio.

Zacks Equity Research

AZN Wins FDA Nod for Expanded Use of Rare Disease Drug, Koselugo

AstraZeneca secures FDA approval to expand Koselugo's use to treat adult NF1 patients with inoperable PN.

Sundeep Ganoria

Here's How ANIP's Rare Disease Portfolio Is Driving Top-line Growth

ANI Pharmaceuticals' rare disease surge, led by Cortrophin Gel, drives major 2025 revenue gains despite softer ophthalmology sales.

Kinjel Shah

PFE's New & Acquired Drugs Drive Non-COVID Comeback as LOE Test Looms

Pfizer's new and acquired drugs lift non-COVID revenue, with recent launches and Seagen products driving momentum into 2026 despite looming LOEs.

Mark Vickery

Top Analyst Reports for Visa, Merck & Southern Company

Visa sees solid volume growth and cross-border gains, while Merck and Southern Company navigate competitive and regulatory pressures.

Ekta Bagri

Will Librexia ACS Study Setback Dent BMY's Cardiovascular Portfolio?

BMY ends its Librexia ACS study after an interim review shows milvexian is unlikely to meet goals, while other late-stage studies continue.

Zacks Equity Research

COGT Stock Skyrockets 120% in a Month: Here's What You Need to Know

Cogent Biosciences soars as its bezuclastinib combo delivers strong phase III GIST results, driving momentum toward key regulatory filings.

Zacks Equity Research

VKTX Completes Enrollment in First Late-Stage Study on Obesity Drug

Viking Therapeutics completes enrollment in its phase III VANQUISH-1 obesity study, surpassing targets and marking rapid progress for its VK2735 program.

Zacks Equity Research

MRK HIV Regimen Meets Goal in New Study, Gains EU Nod for Keytruda SC

Merck reports strong new HIV study results showing non-inferiority of DOR/ISL to Gilead's Biktarvy and secures an EU approval for its faster-to-administer SC version of Keytruda.

Zacks Equity Research

REGN Gets EC Nod for Libtayo Label Expansion, FDA Clears Monthly Eylea HD

Regeneron gains EC approval to expand Libtayo's use in high-risk CSCC. The FDA approves Eylea HD the treatment of patients with macular edema following retinal vein occlusion.