FirstWord Pharma
Coverage by FirstWord Pharma as tracked by Newsylist.
‘Greg, you’ve got to bring back this platform’: How LifeMine won over Gates and Bezos for $188M series E
Takeda’s narcolepsy drug approved by the FDA, seen as a boon for new class of treatments
Amgen drops ph. 1 obesity drug, upping pressure on MariTide
Eli Lilly to allow more patients to apply for special access to unapproved obesity drug
AstraZeneca holds talks with Bristol Myers Squibb over $400bn tie-up
Novo Nordisk shares dive after heart medicine fails trial, dealing another blow to its pipeline
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FDA Panel Votes In Favor of Replimune’s Melanoma Treatment
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Argenx to Buy Forte Biosciences for $2.2 Billion
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Ahead of hearing, FDA questions the efficacy of Capricor’s Duchenne drug
Capricor Therapeutics shares have plunged after FDA staff raised concerns regarding the efficacy and data of its Duchenne heart disease therapy.
Earnings live: AstraZeneca stock rises to kick off a busy earnings week
AstraZeneca shares rise after Q2 2026 earnings beat driven by strong cancer drug sales.
FDA Approves Centanafadine for ADHD in Children, Adolescents, and Adults
Patients aged six and older now have access to SIMTRIYO, the first new-class ADHD medication approved by the FDA in decades.
Sanofi abandons plan to seek approval for eczema drug from $1.1B Kymab buyout
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Eli Lilly’s Anticipated Weight Loss Drug Helped People Lose 56 Pounds On Average
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The 'Best-Case Scenario' That Shot Arrowhead Stock Sky-High
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Alzheimer's: Real-world study confirms Leqembi therapy benefits
FDA approval of an at-home subcutaneous injection for Leqembi marks a shift in the delivery of early Alzheimer's disease treatment.
Johnson & Johnson CFO Says Guidance Hike Is Just the Start
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Roche Lung-Cancer Drug Candidate Beats Existing Therapies in Late-Stage Trial
Roche's drug candidate divarasib outperformed rival therapies in a Phase 3 trial for KRAS-driven lung cancer.
Ipsen to Buy Kartos Therapeutics for Up to $1.75 Billion
French biotech Ipsen is acquiring Kartos Therapeutics in a deal valued at up to $1.75 billion to expand its hemato-oncology pipeline.
European Regulator Calls for Amgen’s Tavneos to Have Authorization Revoked
European regulators are recommending the revocation of marketing authorization for Amgen's rare-disease drug Tavneos following new data.
New Drugs Are Replacing Chemo for Aggressive Breast Cancer
The FDA has granted broad first-line approval for Gilead's Trodelvy, signaling a shift away from traditional chemotherapy for aggressive breast cancer.
Ophthalmology venture grabs investors’ attention, raises $330 million
Sangamo to put ‘substantially all’ assets for sale in bankruptcy, lines up Lilly and Astellas as buyers
Closely watched Pfizer lung cancer drug falls short in clinical trial
HHS Launches Unprecedented Department-Wide Effort to Restore American Leadership in Clinical Trials
The U.S. Department of Health and Human Services is launching a department-wide effort to accelerate clinical trials and restore American leadership in medical research.