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Articles


In a confirmatory trial, Exkivity did not meet the primary endpoint in treating patients with non-small cell lung cancer with EGFR exon 20 mutations. It will remain available while Takeda works with the FDA on withdrawal timing.


Takeda to Withdraw Oncology Drug Exkivity from U.S. Market

Director of Nonprofit Strategy, Patient Advocacy, IQVIA

Patient organizations should focus on how they can be the most effective by leveraging their strengths to uncover new research opportunities.

Maximizing Impact Through Strategic Research Investments That Address Unmet Needs


The FDA has approved several new therapies this week, including a new two-component Pompe therapy, an extended-release drug for major depression without sexual side effects, and an eye drop for drug-induced dilation. Additionally, the agency has set review dates for several products, including odronextamab for blood cancers, sotatercept for pulmonary arterial hypertension, and Dupixent in young children with eosinophilic esophagitis.


FDA Updates for the Week of Sept. 25, 2023

Senior Vice President of Risk Adjustment Solutions for PopHealthCare and Emcara Health.

Jeremy Berk, senior vice president of Risk Adjustment Solutions for PopHealthCare and Emcara Health, shares how plans must conduct a detailed analysis of how changes to risk adjustment models impact your plan in order to set an effective go-forward strategy.

CMS Has Changed the Game for Medicare Advantage Reimbursement. Here’s How Plans Can Respond Effectively.

Managed Healthcare Executive provides C-suite executives at health plans and provider organizations with news, analysis, insights, and strategies to pursue value-driven solutions.

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Straying from the popular opinion of the industry, a handful of medical device manufactures have aligned with Obama's proposed investment in comparative effectiveness research.

Comparative effectiveness needs reimbursement reform

Scott Huennekens

Articles