Endpoints News
A blueprint for generative AI in healthcare Read in browser
Endpoints News
Thank you for reading, dupa dupackia!
basic
UPGRADE
M T W Thu F
10 September, 2026
sponsored by katalyze
Stop Searching Through COAs and Batch Records. Start Asking Them Questions.
Katalyze digitizes COAs, paper batch records, and PDFs, then creates an ontology tailored to your operation and builds a knowledge graph connecting those records with relevant system data. Your teams can search that knowledge and ask questions in plain language, with every answer traceable to its original source. Built for GxP environments, Katalyze puts fragmented records to work across Yield Optimization, Deviation Investigation, and Raw Material Characterization, with your experts in control.
Book a Demo
top stories
1. FDA suggests regulatory flexibility for assessing psychedelics
2. The blueprint for clinical AI
3. FDA places partial hold on Biohaven's ion channel drug
4. Pharma investment in UK picks up after last year’s lull, trade group says
5. How past Endpoints 11 winners fared as the biotech industry rebounded
6.
news briefing
Shionogi's stroke drug fails mid-stage; Bayer's Hyrnuo gets expanded label in NSCLC
more stories
 
Nicole DeFeudis
.

CAR-Ts have been generating a lot of excitement in oncology. But recently disclosed trial deaths have raised questions about their use in autoimmune disease. In an interview with Merck, I asked why it doesn't have any CAR-Ts in its core pipeline. Oncology clinical development head Marjorie Green cited logistical issues and the challenges of scaling the personalized therapies for patients. (In contrast, the production of its Moderna-partnered personalized cancer vaccine is an “easier process,” she said.)

.
Nicole DeFeudis
Senior Reporter, Endpoints News
@Nicole_DeFeudis
1
by Nicole DeFeudis

FDA reg­u­la­tors said they’re open to “in­no­v­a­tive ap­proach­es” for study­ing the ef­fects of psy­che­del­ic ther­a­pies, in­clud­ing the use of com­para­tors oth­er than place­bo.

The com­ments...

Read the full story
2
by Shelby Livingston

ARPA-H, a fed­er­al agency that funds break­through health tech­nolo­gies, just kicked off a new pro­gram called AD­VO­CATE that pro­vides mil­lions of dol­lars to health tech...

Read the full story
Health Tech Day 2026
The entire healthcare ecosystem is more Silicon Valley-ified than ever before. What tech has actually changed? Is biopharma behind? Find out, join us for Health Tech day.
3
by Max Gelman

The FDA has placed a trou­bled Bio­haven pro­gram on par­tial clin­i­cal hold, the com­pa­ny dis­closed Wednes­day.

An epilep­sy study of the ex­per­i­men­tal drug called BHV-7000...

Read the full story
4
by Anna Brown

The UK gov­ern­men­t's move to pay more for med­i­cines and fos­ter a clos­er re­la­tion­ship with drug­mak­ers ap­pears to have led to an in­crease in the...

Read the full story
5
by Kyle LaHucik

We'll be un­veil­ing this year's End­points 11 in Boston on the night of Sept. 24. Join us.

The bio­phar­ma in­dus­try feels much dif­fer­ent than...

Read the full story
News Briefing: Quick hits from the biopharma web
6
by ENDPOINTS

Plus news about Tevard Bio­sciences, Disc Med­i­cine, InduPro, EMD Serono and Fra­zier Life Sci­ences.

Sh­iono­gi fails mid-stage stroke tri­al: The com­pa­ny’s ex­per­i­men­tal drug redasemtide didn’t...