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Akebia Therapeutics Reports Second Quarter 2021 Financial Results and Highlights Recent Company Milestones

Akebia Therapeutics Reports Second Quarter 2021 Financial Results and Highlights Recent Company Milestones
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Merck s KEYTRUDA® Significantly Prolonged Recurrence-Free Survival Compared to Placebo as Adjuvant Therapy for Patients With Stage II Resected High-Risk Melanoma in Phase 3 KEYNOTE-716 Trial

Merck s KEYTRUDA® Significantly Prolonged Recurrence-Free Survival Compared to Placebo as Adjuvant Therapy for Patients With Stage II Resected High-Risk Melanoma in Phase 3 KEYNOTE-716 Trial
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Amgen Reports Second Quarter 2021 Financial Results

Amgen Reports Second Quarter 2021 Financial Results Amgen today announced financial results for the second quarter of 2021. Key results include: Total revenues increased 5% to $6.5 billion in comparison to the second quarter of 2020, driven by higher unit demand, partially offset by lower net selling prices. Product sales increased 3% globally, driven by double digit volume growth across a number of our products including Prolia ® Repatha ® and our biosimilar … – Amgen (NASDAQ:AMGN) today announced financial results for the second quarter of 2021. Key results include: Total revenues increased 5% to $6.5 billion in comparison to the second quarter of 2020, driven by higher unit demand, partially offset by lower net selling prices.

These Are The Top Priorities Challenges For New CDER Director Patrizia Cavazzoni MD

These Are The Top Priorities & Challenges For New CDER Director Patrizia Cavazzoni, M.D. By Lowell M. Zeta and Lynn Mehler, Hogan Lovells Scientific breakthroughs have revolutionized the development of new and more personalized therapies to address unmet medical needs through enhanced technologies and data-informed capabilities. Advances in data infrastructure, clinical trial design, and other medical product technologies and the 21st Century Cures Act and other legislation aim to bring new innovations to patients who need them faster. These developments are requiring the FDA to rethink the ways it applies and interprets the law and to speed up its efforts to adopt innovative scientific approaches to inform regulatory decisions that make products more effective, safer, and available sooner.

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