---
title: "GSK licenses Chinese trispecific T‑cell engager for multiple myeloma; FDA urged on psychedelic sta"
id: "stat-news-2-stat-pharmalittle-we-re-reading-about-a-gsk-deal-for-a-drug-from-china-job"
canonical_url: "https://medichelpline.com/clinical-feed/stat-news-2-stat-pharmalittle-we-re-reading-about-a-gsk-deal-for-a-drug-from-china-job"
content_type: "clinical_feed_article"
specialty: "Oncology"
source_name: "STAT News"
source_url: "https://www.statnews.com/pharmalot/2026/09/15/gsk-china-drug-licensing-deal-job-losses/?utm_campaign=rss"
published_at: "2026-09-15T13:29:47.000Z"
evidence_level: "Verified Feed"
license: "CC-BY-NC-4.0 / Informational Use"
---
# GSK licenses Chinese trispecific T‑cell engager for multiple myeloma; FDA urged on psychedelic sta
## Provenance & Clinical Metadata
- **Canonical URL:** https://medichelpline.com/clinical-feed/stat-news-2-stat-pharmalittle-we-re-reading-about-a-gsk-deal-for-a-drug-from-china-job
- **Specialty:** [Oncology](https://medichelpline.com/clinical-feed/oncology.md)
- **Primary Source:** STAT News
- **Source URL:** [Original Journal Publication](https://www.statnews.com/pharmalot/2026/09/15/gsk-china-drug-licensing-deal-job-losses/?utm_campaign=rss)
- **Published At:** 2026-09-15T13:29:47.000Z
- **Evidence Rating:** Verified Feed
## Executive GIST (TL;DR)
- The U.S. FDA held a four‑hour public meeting where clinicians and others urged the agency to establish clear safety and access standards for **psychedelic therapies**, addressing provider training, patient screening and monitoring, reimbursement, clinic capacity, and long‑term safety data collection. The meeting occurred amid an administration push to accelerate psychedelic programs. - **GSK** struck a deal to acquire global rights to a multiple myeloma candidate developed by China’s Chimagen Biosciences for up to $750 million. The candidate is described as a “potential first‑in‑class” **trispecific T‑cell engager** currently in preclinical development. - GSK says the trispecific TCE aims to provide targeted activity against **multiple myeloma** cells with improved safety compared with existing TCEs, which have had challenging tolerability profiles. Human testing for the candidate is expected to begin next year, according to the reporting. - Details beyond these items — including the identity of the candidate and additional transactional specifics — were not reported in the source story excerpt and the full Pharmalot piece is available behind a STAT+ paywall. - Coverage drew on reporting by Reuters for the FDA hearing and Pharmaphorum for the GSK‑Chimagen licensing transaction; the STAT excerpt notes additional content is subscriber‑gated.
## Clinical Analysis & Structured Key Points
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Test your knowledge with our new weekday mini crossword [ Start solving ](https://www.statnews.com/stat-mini-crossword/) [STAT Plus](https://www.statnews.com/stat-plus/)Newsletter[Pharmalot](https://www.statnews.com/category/pharma/pharmalot/) # 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](https://www.statnews.com/my-account/edit/#emails) * Email this article * [Share this article](https://www.statnews.com/pharmalot/2026/09/15/gsk-china-drug-licensing-deal-job-losses/?utm_campaign=rss) ![an anthropomorphized red and blue pill illustrated in the style of the famous american gothic painting](https://www.statnews.com/wp-content/uploads/2015/11/PHARMALOT_LITTLE-copy-645x645.jpg) Alex Hogan/STAT ![](https://www.statnews.com/wp-content/uploads/2021/02/ed-s-avatar-small4-80x80.png) By [Ed Silverman](https://www.statnews.com/staff/ed-silverman/) Sept. 15, 2026 Pharmalot Columnist, Senior Writer ![](https://www.statnews.com/wp-content/uploads/2021/02/ed-s-avatar-small4-80x80.png) [Ed Silverman](https://www.statnews.com/staff/ed-silverman/) 1. [](https://www.linkedin.com/in/edsilverman/ "Linkedin") 2. [](https://x.com/Pharmalot "X") ed.silverman@statnews.com 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](https://www.statnews.com/signup/pharmalittle/) and the afternoon [Pharmalot newsletter](https://www.statnews.com/signup/pharmalot/). 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](https://store.bostonglobe.com/collections/stat-news/products/pharmalot-mug). 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](https://www.reuters.com/legal/litigation/fda-hold-public-hearing-psychedelic-drugs-trump-driven-push-gathers-pace-2026-09-14/) 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](https://pharmaphorum.com/news/gsk-wagers-750m-chimagen-multiple-myeloma-therapy) 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. [![STAT+](https://www.statnews.com/wp-content/themes/stat/images/stat-plus-logo.svg)](https://www.statnews.com/stat-plus/) To read the rest of this story subscribe to STAT+. 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