---
title: "U.S. Plans Rules to Preserve Most Pharma Licensing Deals With China, Plus Reports on Post‑Market S"
id: "stat-news-2-stat-pharmalittle-we-re-reading-about-licensing-deals-with-china-making-drugs"
canonical_url: "https://medichelpline.com/clinical-feed/stat-news-2-stat-pharmalittle-we-re-reading-about-licensing-deals-with-china-making-drugs"
content_type: "clinical_feed_article"
specialty: "Pharmacology"
source_name: "STAT News"
source_url: "https://www.statnews.com/pharmalot/2026/09/18/rules-for-china-licensing-deals-making-drugs-in-space/?utm_campaign=rss"
published_at: "2026-09-18T13:29:38.000Z"
evidence_level: "Verified Feed"
license: "CC-BY-NC-4.0 / Informational Use"
---
# U.S. Plans Rules to Preserve Most Pharma Licensing Deals With China, Plus Reports on Post‑Market S
## Provenance & Clinical Metadata
- **Canonical URL:** https://medichelpline.com/clinical-feed/stat-news-2-stat-pharmalittle-we-re-reading-about-licensing-deals-with-china-making-drugs
- **Specialty:** [Pharmacology](https://medichelpline.com/clinical-feed/pharmacology.md)
- **Primary Source:** STAT News
- **Source URL:** [Original Journal Publication](https://www.statnews.com/pharmalot/2026/09/18/rules-for-china-licensing-deals-making-drugs-in-space/?utm_campaign=rss)
- **Published At:** 2026-09-18T13:29:38.000Z
- **Evidence Rating:** Verified Feed
## Executive GIST (TL;DR)
- The U.S. Treasury Department is drafting rules that would likely allow U.S. pharmaceutical companies to pursue most **licensing deals with China**, while restricting investment related to pathogens or biotechnology that could be weaponized. The approach would be less restrictive than proposals from some lawmakers and differ from the Trump administration’s tighter posture on other industries. - A separate analysis of U.S. Food and Drug Administration data, reported by **KFF Health News**, found hundreds of **post‑market studies** listed as delayed; some delays span more than a decade or remain without a finalized plan. Reliance on post‑approval studies to resolve questions creates safety and cost risks for patients, payers, and public programs. - The piece notes reporting that **Anthropic** quietly established a laboratory to perform physical biology work as it expands into drug science; the source presents this development but the article text available here did not provide further operational or timeline details. - Much of the original Pharmalot column is behind a STAT+ paywall; additional items and in‑depth coverage referenced in the original are not accessible in the provided source text. Consequently, some story details and supplementary examples were not reported in the visible content. - Overall, the visible reporting highlights regulatory and safety concerns at the intersection of global biotech investment, post‑market surveillance, and emerging entrants from tech into drug science. The Treasury’s drafting signals an intent to balance commercial engagement with national security limits, while the KFF analysis raises questions about the enforcement and timeliness of post‑approval study commitments.
## Clinical Analysis & Structured Key Points
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[](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/). And so, another working week will soon come to a close. Not a moment too soon, yes? This is, you may recall, our treasured signal to daydream about weekend plans. Our agenda is still taking shape, but we plan on promenading with the official mascots, catching up on our reading, escorting Mrs. Pharmalot to a speakeasy and, if time permits, holding another listening party, where the rotation will likely feature [this](https://youtu.be/kvTbdUwBzZ0?si=kNEWIXVNyTSYBvBk), [this](https://youtu.be/UIkMeaAfIRw?si=CvRGiq8XpCnk8vKA), [this](https://youtu.be/51YIBK9Jdy0?si=mPZqCgDQmQn9si_7), [this](https://youtu.be/WHTxhiRkL84?si=LNHQ4FE1V8ZRu8PF) and [this](https://youtu.be/qHEPHPHuNis?si=eAqKn-d0__Wzp4ea). And what about you? Now that autumn is upon us, this is a fine time to jump in your jalopy to visit orchards and patches. If the weather fails to cooperate, you could binge-watch a few series on the telly or shop for warmer garb. Maybe a new sweater or two is needed. Or stop by the eatery that always appeared inviting. Well, whatever you do, have a grand time. But be safe. Enjoy, and see you on Tuesday, since we will be off again to observe ancient rituals and a pinch hitter will be in our stead on Monday. … **The U.S. is working on rules for pharmaceutical companies investing in China that would likely preserve their ability to strike most licensing deals for Chinese drugs,** [Reuters](https://www.reuters.com/world/us-weighs-allowing-most-pharma-licensing-deals-with-china-sources-say-2026-09-18/) reports. This would mark a departure for the Trump administration, which has sought to tighten business ties with China for other industries under new national security legislation, and would be looser than restrictions sought ‌by some lawmakers. The rules, being drafted by the U.S. Treasury Department, are likely to allow U.S. drugmakers to invest in promising new drugs being developed by Chinese companies as long as they are not related to pathogens or biotechnology that could be weaponized. Advertisement **An analysis of U.S. Food and Drug Administration data found hundreds of post-market studies listed as delayed and, in some cases, the work was delayed by more than a decade or the manufacturer was still developing a plan for the study** , [KFF Health News](https://kffhealthnews.org/health-industry/fda-approval-drugs-medical-devices-postmarket-studies-safety-delays-amgen-tavneos/?utm_campaign=KHN%3A%20First%20Edition&utm_medium=email&_hsenc=p2ANqtz-9rdWPP-zQkfORYej9NF_QZ0zzHS__Y0M54sCrHmgvBAkKr4Y2bD5dyRS28B-xDOupaN8eb8I65IrtpRPxiC4FgZdYjkg&_hsmi=439625386&utm_content=439625386&utm_source=hs_email) confides. Relying on post-approval studies to resolve questions risks exposing patients to products that do more harm than good. Whoever is paying the bills — patients, insurance companies, employers, or government health programs such as Medicare and Medicaid — can end up wasting money and rewarding manufacturers for useless or risky products. 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