News Archive

News Archive - Page 12 of 30 - Real Endpoints

May 12, 2023

Bristol-Myers Squibb’s Giovanni Caforio is handing the baton to Chris Boerner

With the news that Giovanni Caforio is handing the baton to Chris Boerner, I think we can say we called this one right. In all seriousness, it's no surprise to us that companies recognize the importance of putting people with deep market access roots into leadership positions. The commercial landscape is only growing more complex.

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Apr 13, 2023

Real Endpoints announces four biopharma clients have signed on as customers for RE Assist, a tech-enabled AI platform providing real-time foundation fund information to Medicare patients

Real Endpoints, the leading market-access platform and advisory firm, announces that four biopharma companies with combined 2022 sales of nearly $8 billion have signed contracts to offer Real Endpoint's RE Assist tool to support Medicare patients in need of deductible and copay assistance. RE Assist provides actionable, comprehensive foundation fund information in a compliant and easy to navigate format.

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Apr 12, 2023

Gene Therapies and Gene Editing – invitation-only meeting

The use of warranties – and more broadly, outcomes-based contracting - is a topic that’s sure to come up in an invitation-only meeting I am co-hosting with Roger Longman and Jeff Berkowitz from Real Endpoints, as well as LEK’s Pierre Jacquet and Orsini’s Nick Calla.

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Mar 27, 2023

Real Endpoints at AMCP

Thanks to AMCP for hosting a session on value based contracting in healthcare at this year's annual meeting in San Antonio. The packed house underscored how important it is to find alignment between payers and manufacturers to increase market access for transformative therapies. Thanks to Michael A. Ford, R.Ph. and moderator Dean Hakanson MD for joining Real Endpoints' Jane F. Barlow, MD, MPH, MBA in sharing their views.

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Mar 27, 2023

Drugmakers push back on a clever tactic employers use to avoid paying for specialty medicines.

Having just returned from the Informa Access USA conference, we can confirm that the so-called “specialty carve out” or “alternative funding” tactics being used by third-party brokers remain a hot topic of discussion.

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Mar 22, 2023

Top FDA official: Agency needs to start using accelerated approval for gene therapies.

At the recent annual meeting of the Muscular Dystrophy Association, Peter Marks, head of the Center for Biologics Evaluation and Research, noted the importance of using the accelerated approval channel for gene therapies: "We can’t be so careful about our approvals under accelerated approval that we prevent potentially lifesaving therapies from getting to market in a timely manner," he said.

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Mar 21, 2023

Visit Real Endpoints at Access USA

Stop by Booth #110 at Access USA to meet the Real Endpoints team! We're showcasing RE Assist, a tech-enabled platform that simplifies the process of finding copay assistance for Medicare patients.

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Mar 21, 2023

Yesterday, the Centers for Medicare & Medicaid Services updated its guidance for drug price negotiation under the Inflation Reduction Act

Seems like the biopharma industry, not just Caesar, should beware the ides of March. Yesterday, the Centers for Medicare & Medicaid Services updated its guidance for drug price negotiation under the Inflation Reduction Act clarifying that drugs with the same active ingredients will be groups together even if they are approved under different biologic license applications. That suggests that different formulations (say a sub-cue version of an infusion product developed earlier) would be subject to price negotiation at the earliest date of eligibility.

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