New & Notable
FTC’s PBM insulin price case stalled after Trump firings
FTC’s suit over PBM insulin pricing is stalled after Trump fired two Democratic FTC commissioners, leaving the agency without enough members to forward.
FDA winds down GLP-1 compounding policies
With semaglutide and tirzepatide shortages resolved, the FDA has set firm deadlines ending temporary compounding policies, marking a major shift as the GLP-1 market stabilizes.
Expanding orphan drug access for rare conditions
Incentives have accelerated orphan drug development, turning rare disease treatments into one of the fastest-growing and most innovative sectors in the biopharmaceutical industry.
Orphan drugs will double their market share by 2030
By 2030, orphan drugs will double their market share to 20% of the $1.6 trillion global drug market, with a CAGR of over 10%, outperforming the 7.5% of non-orphan drugs.
Insights
Insights is research conducted by and for TechTarget Xtelligent Healthcare. Our work aims to leverage Xtelligent’s diverse readership of healthcare professionals across various sectors of the industry to understand real-world challenges and identify effective solutions.
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Healthcare Strategies: A Podcast
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A podcast for healthcare professionals seeking solutions to today's and tomorrow's top challenges. Hosted by the editors of Xtelligent Healthcare Media, this podcast series focuses on real-world use cases that are leading to tangible improvements in care quality, outcomes, and cost.
Guests from leading provider, payer, government, and other organizations share their approaches to transforming healthcare in a meaningful and lasting way.
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Latest News
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Big Pharma's $13.8B DTC ad spend drives drug costs
A CSRxP report reveals Big Pharma spent $13.8B on direct-to-consumer advertising in 2023, prompting renewed calls to eliminate corporate tax deductions worth up to $1.7B annually.
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Medical device report delays raise safety concerns
A BMJ study finds nearly one-third of medical device makers submit adverse event reports late, with 54.8% linked to 3 manufacturers and 13 devices, raising safety concerns.
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AI prior authorization denials threaten patient care
AMA survey warns that 61% of physicians are alarmed by AI-driven prior authorization, with denials delaying care and contributing to serious patient harm.
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FDA approves Merilog, first NovoLog biosimilar for diabetes
The FDA approved Merilog (insulin-aspart-szjj), the first biosimilar to NovoLog, enhancing insulin accessibility and competition while potentially lowering costs.
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Emerging vision risks linked to semaglutide, tirzepatide
Recent data points to potential ophthalmic complications, including optic neuropathy and maculopathy, in patients treated with semaglutide and tirzepatide.
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FDA approves Journavx, a safer painkiller alternative
The FDA's approval of Journavx, a first-in-class non-opioid analgesic for acute pain, marks a breakthrough that could reshape pain management and reduce reliance on opioids.
Features
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Understanding spread pricing, how PBMs influence drug costs
PBM spread pricing raises drug costs by keeping the difference between insurer charges and pharmacy payouts, fueling demand for transparency and alternative pricing models.
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Optimizing prior authorization with AI-driven efficiency
As prior authorization poses a hurdle in healthcare, AI-driven solutions are reshaping the process by reducing delays, improving efficiency and minimizing administrative burdens.
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Exploring FDA-approved biosimilar insulin products
FDA-approved biosimilar insulin products, such as Semglee, Rezvoglar and Merilog, expand access and provide cost-effective alternatives to reference biologics.
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How AI is revolutionizing clinical trials, drug development
AI is transforming clinical trials by enhancing patient recruitment, site selection and data analysis. These advancements accelerate drug development while reducing costs.