
HCPLive 5 Stories in Under 5: Week of 09/07
Key Takeaways
- The FDA opted not to convene an advisory committee for sparsentan's sNDA in FSGS, with a decision due in January 2026.
- Intercept is withdrawing obeticholic acid from the US PBC market after an FDA request and clinical trial holds.
An audio recap of the top 5 stories in healthcare news from the week of 9/5-9/13.
Welcome to HCPLive's 5 Stories in Under 5—your quick, must-know recap of the top 5 healthcare stories from the past week, all in under 5 minutes. Stay informed, stay ahead, and let’s dive into the latest updates impacting clinicians and healthcare providers like you!
Interested in a more traditional, text rundown?
Top 5 Healthcare Headlines for September 5-September 13, 2025:
1.
The FDA determined no advisory committee is needed for sparsentan’s sNDA in FSGS, which remains under review with a January 2026 decision date.
2.
Intercept will withdraw obeticholic acid from the US PBC market after an FDA request and related clinical trial holds.
3.
The FDA accepted a proposal to qualify FibroScan liver stiffness measurement as a surrogate endpoint for MASH trials, supported by multiple industry partners.
4.
eGenesis received FDA clearance to begin clinical testing of a genetically engineered porcine kidney transplant in patients with ESKD.
5.
Regeneron reported phase 3 success for novel allergen-blocking antibodies targeting cat and birch allergies, with confirmatory trials planned.















































































