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Grafa
Health

Bristol Myers Squibb announces positive Phase 3 results for Mezigdomide in MM

Bristol Myers Squibb reached a major milestone in its next-generation protein degradation program on Monday, reporting that its oral CELMoD agent, mezigdomide, significantly extended the time patients lived without their cancer progressing in a pivotal Phase 3 study.

Read more: Bristol Myers Squibb announces positive Phase 3 results for Mezigdomide in MM
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Health

Pfizer's Tilrekimig hits primary endpoint in atopic dermatitis Phase 2 trial

Pfizer announced positive topline results for its investigational trispecific antibody, tilrekimig, which demonstrated significant skin clearance in adults with moderate to severe eczema and paved the way for a pivotal Phase 3 study later this year.

Read more: Pfizer's Tilrekimig hits primary endpoint in atopic dermatitis Phase 2 trial
Grafa
Technology

Korn Ferry fee revenue surges 7% as digital and consulting demand diversifies

Korn Ferry (NYSE:KFY) reported a strong third quarter for fiscal 2026, with fee revenue reaching $717.4 million as the global consulting firm successfully leveraged high-growth digital services and long-term contracts to offset broader economic shifts.

Read more: Korn Ferry fee revenue surges 7% as digital and consulting demand diversifies
Grafa
Technology

BETA Technologies post-IPO revenue surges 135% on electric motor deliveries

BETA Technologies reported a significant jump in full-year 2025 revenue following its market debut, as the electric aerospace pioneer scales its charging infrastructure and begins high-volume deliveries of its proprietary propulsion systems.

Read more: BETA Technologies post-IPO revenue surges 135% on electric motor deliveries
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Health

FDA grants priority review to Enhertu for high-risk early breast cancer

AstraZeneca (NASDAQ:AZN) and Daiichi Sankyo moved a step closer to a major label expansion for their blockbuster cancer therapy, Enhertu, after the U.S. FDA fast-tracked an application to treat patients with early-stage breast cancer at high risk of recurrence.

Read more: FDA grants priority review to Enhertu for high-risk early breast cancer
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Health

Adial Pharmaceuticals narrows 2025 loss, clears regulatory hurdles for AD04

Adial Pharmaceuticals (NASDAQ:ADIL) reported a significant reduction in annual net losses for 2025, as the clinical-stage biotech firm secures FDA alignment and strategic partnerships to transition its lead alcohol-use disorder candidate into Phase 3 trials.

Read more: Adial Pharmaceuticals narrows 2025 loss, clears regulatory hurdles for AD04
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Halozyme partner J&J wins FDA nod for myeloma combo featuring ENHANZE tech

Halozyme Therapeutics (NASDAQ:HALO) shares were in focus Friday after partner Johnson & Johnson secured U.S. regulatory approval for a subcutaneous combination therapy that significantly reduces the risk of disease progression in patients with relapsed multiple myeloma.

Read more: Halozyme partner J&J wins FDA nod for myeloma combo featuring ENHANZE tech
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Health

PMV Pharmaceuticals secures orphan drug status as ovarian cancer data strengthens

PMV Pharmaceuticals (NASDAQ:PMVP) reported significant clinical momentum for its lead candidate, rezatapopt, bolstered by a fresh FDA Orphan Drug Designation and clinical results showing high response rates in late-stage ovarian cancer patients.

Read more: PMV Pharmaceuticals secures orphan drug status as ovarian cancer data strengthens