STAT+: Pharmalittle: We’re reading about a GSK deal for a drug from China, job losses in the U.S., and more

STAT PlusNewsletterPharmalot Pharmalittle: We’re reading about a GSK deal for a drug from China, job losses in the U.S., and more FDA urged to create clear safety ‌and access standards for psychedelics Manage alerts for this article Email this article Share this article By Ed SilvermanSept. 15, 2026 Pharmalot Columnist, Senior Writer Ed Silverman[email protected]Ed’s stories explore prescription drug pricing, affordability and access, as well issues surrounding patents, litigation, and legislation. He is also the author of the morning Pharmalittle newsletter and the afternoon Pharmalot newsletter.

Rise and shine, everyone, another busy day is on the way. And it is getting off to a pleasant start here on the Pharmalot campus, where clear blue skies and comfy breezes are greeting us. As for the official mascots, they are happily snoozing in their respective corners.

As for us, we are firing up the trusty kettle for another cuppa stimulation. Our choice today is ginger peach. Of course, you are invited to join us.

For the full experience, we are now hawking replicas — take a look. Meanwhile, here are a few items of interest. As always, do keep in touch.

We appreciate feedback, criticism, and tips. … Doctors, veterans, pharmacists, and therapists urged the U.S. Food and Drug Administration to establish clear safety ‌and access standards for psychedelic therapies during a four-hour public meeting on Monday convened by the agency amid efforts to speed development, Reuters reports.

The hearing was the latest in a months-long push by the Trump administration to bring qualified psychedelic drug programs to market. Discussions at the ​meeting focused on practical issues that could shape how psychedelic therapies are tested and delivered, including provider training ​and credentials, patient screening and monitoring, access and reimbursement, clinic capacity, and collecting long-term ⁠safety data.Advertisement GSK has continued its drive to bulk up its pipeline, taking global rights to a multiple myeloma treatment, which was developed by China’s Chimagen Biosciences, for up to $750 million, Pharmaphorum writes. The deal focuses on a “potential first-in-class” trispecific T-cell engager that, according to GSK, promises to combine good targeting of multiple myeloma cells but also offer improved safety compared to other TCEs for the blood cancer, which it says have suffered from “difficult tolerability profiles.” Chimagen’s unidentified candidate is currently in preclinical-stage development and due to start human testing next year.

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Subscribe Log In pharmalittle, STAT+ Submit a correction requestReprints Ed Silverman Pharmalot Columnist, Senior Writer Ed’s stories explore prescription drug pricing, affordability and access, as well issues surrounding patents, litigation, and legislation. He is also the author of the morning Pharmalittle newsletter and the afternoon Pharmalot newsletter. Newsletter Understand how science, health policy, and medicine shape the world every day Recommended Pharmalot September 14, 2026 STAT Plus: Pharmalittle: We’re reading about another AstraZeneca trial failure, a Novo name change, and more Pharmalot September 13, 2026 STAT Plus: Trump’s secretive pharma deals may undermine ‘most-favored nation’ pricing, an analysis suggests Advertisement Pharmalot September 11, 2026 STAT Plus: Pharma wins a battle over the cost of wastewater treatment in Europe Pharmalot September 11, 2026 STAT Plus: Up and down the ladder: The latest comings and goings Pharmalot September 11, 2026 STAT Plus: Pharmalittle: We’re reading about anxious Novartis investors, patent expirations for biologics, and more Subscriber Picks