News|Podcasts|March 19, 2026

Pharmaceutical Executive Daily: Analysis on TrumpRx List Pricing

In today's Pharmaceutical Executive Daily, a new analysis finds that TrumpRx is listing prices for roughly a third of its featured drugs higher than what patients in the United Kingdom pay, two biotech companies focused on next-generation T-cell engager therapies close significant funding rounds, and Pharmaceutical Executive sits down with Jeanne Marrazzo of the Infectious Diseases Society of America on the worsening U.S. measles outbreak and what it means for the future of vaccine confidence.

Welcome to Pharmaceutical Executive Daily, your quick briefing on the top news shaping the pharmaceutical and life sciences industry.

In today's Pharmaceutical Executive Daily, a new analysis finds that TrumpRx is listing prices for roughly a third of its featured drugs higher than what patients in the United Kingdom pay, two biotech companies focused on next-generation T-cell engager therapies close significant funding rounds, and Pharmaceutical Executive sits down with Jeanne Marrazzo of the Infectious Diseases Society of America on the worsening U.S. measles outbreak and what it means for the future of vaccine confidence.

A Reuters comparison of TrumpRx pricing against UK National Health Service data found that prices for approximately a third of the 54 drugs listed on the administration's direct-to-consumer platform were lower in the UK, including several medications that were between 67% and 82% cheaper abroad. Critics have noted that the most-favored-nation agreements underlying TrumpRx are voluntary and carry no enforcement mechanisms, and that the platform reflects cash prices rather than what most insured Americans actually pay at the pharmacy.

In funding news, Excalipoint Therapeutics has emerged with an oversubscribed $68.7 million seed round, one of the largest early-stage raises for a Chinese biotech, to advance six T-cell engager programs targeting solid tumors and difficult-to-treat cancers across three proprietary platforms. Separately, Crossbow Therapeutics has closed a $77 million Series B to continue its Phase 1 trial of CBX-250, a first-in-class TCE targeting a peptide HLA complex found on myeloid cancer cells, with initial data expected by the end of 2026.

Finally, in a Q&A with Pharmaceutical Executive, Jeanne Marrazzo, CEO of the Infectious Diseases Society of America, describes the current measles outbreak as the largest the United States has seen in decades, one large enough that the country has already lost its measles elimination status. Marrazzo attributes the resurgence to a growing pool of unvaccinated individuals, the extreme transmissibility of the virus, and conflicting messaging from federal health officials that has eroded public trust in vaccines.

Thanks for listening to Pharmaceutical Executive Daily. For more updates and in-depth analysis, visit PharmExec.com.


Related to this article

Pharmaceutical Executive Daily
FDA approves Ultragenyx's Fayuvi as the first treatment for Sanfilippo syndrome type A, Lisata Therapeutics acquires Marea Therapeutics as mAbxience partners with Sandoz on a hemophilia A biosimilar, and Joe Cunningham argues that executive drug-pricing deals alone won't fix costs.
Pharmaceutical Executive daily
FDA approves Kerendia as the first new treatment for kidney disease in type 1 diabetes in decades, Novo, Roche, and Aethlon Medical strike major deals and mergers with Orbis Medicines, Dualitas Therapeutics, and North Immunology, and Thani Jambulingam of Saint Joseph's University examines the fight to control the GLP-1 patient journey.
Pharmaceutical executive daily
GSK is acquiring a trispecific T-cell engager from Chimagen Biosciences and Sanofi expanding its manufacturing partnership with Cheplapharm, Stewart Gandolf discusses why pharma marketing now has to write for both people and AI, and Dr. Elena Christofides explains why cortisol dysregulation may be the hidden reason some diabetes patients fail to respond to incretin therapies.