Endpoints News
Tariffs, drug-pricing deals 'worrisome' for small biotechs: Rhythm CEO Read in browser
Endpoints News
Thank you for reading, dupa dupackia!
basic
UPGRADE
Mon T W Th F
13 April, 2026
US Deals Outlook 20226: What's ahead for pharma and life sciences
US biopharma still leads the world in high-risk drug development, but the road from innovation to access has never been harder to predict. Hear from top executives and investors on how they’re navigating what’s next. Join us.
top stories
1. Exclusive: FDA narrows in on search for new biologics and vaccines leader
2. White House policies are ‘incredibly worrisome’ for small biotechs, Rhythm CEO says 
3. Revolution Medicines' pancreatic cancer drug doubles survival time in Phase 3
4.
news briefing
Neomorph raises $100M for molecular glues; Spyre's ulcerative colitis data
more stories
 
Lydia Ramsey Pflanzer
.

FDA is narrowing its search for a CBER director to replace outgoing leader Vinay Prasad. Zachary Brennan, Max Bayer and Drew Armstrong have the scoop on a leading candidate for today's newsletter.

.
Lydia Ramsey Pflanzer
Deputy Editor, Endpoints News
Houman Hemmati (Novateur Ventures)
1
by Zachary Brennan, Max Bayer, Drew Armstrong

The FDA is get­ting clos­er to an­nounc­ing a di­rec­tor of the Cen­ter for Bi­o­log­ics Eval­u­a­tion and Re­search, sources told End­points News, fol­low­ing the con­tro­ver­sial tenure of out­go­ing leader Vinay Prasad.

A lead­ing can­di­date for the post is Houman Hem­mati, peo­ple who spoke on con­di­tion of anonymi­ty told End­points. Hem­mati is a long­time biotech ex­ec­u­tive and oph­thal­mol­o­gist who has served in more than a dozen in­dus­try roles, posts heav­i­ly on so­cial me­dia and has raised ques­tions about the Covid-19 vac­cine.

Hem­mati didn’t re­spond to a re­quest for com­ment on Mon­day. An HHS spokesper­son told End­points, "No de­ci­sion has been made on the se­lec­tion of the next CBER di­rec­tor. We con­tin­ue to vet high­ly qual­i­fied can­di­dates."

Click here to continue reading
Drug Discovery Day 2026
AI has gone from buzzword to pipeline strategy — but are the results a mixed bag? We're talking to the researchers in the thick of it about what's moving the needle, what's stalling out and what comes next. Join us for a free virtual program, then continue the conversation at an in-person-only fireside and happy hour in Boston. Choose your pass.
Rhythm Pharmaceuticals CEO David Meeker
2
by Anna Brown

Biotechs with sin­gle prod­ucts in the mar­ket are like­ly on edge about how Pres­i­dent Don­ald Trump’s phar­ma tar­iffs and “most fa­vored na­tion” pric­ing will play out, Rhythm Phar­ma­ceu­ti­cals CEO David Meek­er told End­points News in an in­ter­view.

The Boston-based rare dis­ease biotech mar­kets Im­civree for weight man­age­ment in pa­tients with cer­tain rare ge­net­ic dis­or­ders. Meek­er said sim­i­lar com­pa­nies with one com­mer­cial prod­uct may al­so have con­cerns that if they launched their drugs over­seas first, that typ­i­cal­ly low­er price would al­so be­come the list price in the US un­der po­ten­tial MFN pric­ing ne­go­ti­a­tions.

Trump an­nounced 100% phar­ma levies this month, but on­ly some phar­ma com­pa­nies are like­ly to shoul­der those tar­iffs in full. MFN pric­ing deals be­tween drug­mak­ers and the White House ex­empt com­pa­nies from phar­ma tar­iffs.

Click here to continue reading
Mark Goldsmith, Revolution Medicines CEO (Mark Kauzlarich/Bloomberg via Getty Images)
3
by Lei Lei Wu

Rev­o­lu­tion Med­i­cines re­port­ed Mon­day that its ex­per­i­men­tal RAS in­hibitor called darax­on­ra­sib suc­ceed­ed in a reg­is­tra­tional tri­al for pan­cre­at­ic can­cer.

And now, the com­pa­ny plans to ask the FDA to ap­prove the ther­a­py un­der the agency’s Com­mis­sion­er’s Na­tion­al Pri­or­i­ty Vouch­er pro­gram that’s meant to speed up re­view times for a small num­ber of se­lect­ed drugs.

In a Phase 3 tri­al, darax­on­ra­sib led pa­tients with metasta­t­ic pan­cre­at­ic duc­tal ade­no­car­ci­no­ma to sur­vive for a me­di­an 13.2 months com­pared to 6.7 months with chemother­a­py, the com­pa­ny said. That means darax­on­ra­sib cut the risk of death by 60% ver­sus chemother­a­py.

“Break­ing the one-year bar­ri­er in pan­cre­at­ic can­cer is an enor­mous achieve­ment,” Rev­o­lu­tion Med­i­cines CEO Mark Gold­smith told End­points News.

Click here to continue reading
News Briefing: Quick hits from the biopharma web
4
by ENDPOINTS

Plus, news about Ab­b­Vie, Syn­Ox, Eli Lil­ly's Jaypir­ca, Im­a­geneBio, Nx­era Phar­ma, Neu­ro­crine and No­var­tis:

Neo­morph rais­es $100M more for mol­e­c­u­lar glues: San Diego-based Neo­morph has raised a $100 mil­lion Se­ries B round led by its found­ing in­vestor, Deer­field Man­age­ment. The start­up dosed its first pa­tient in Feb­ru­ary in a tri­al of NEO-811, its lead mol­e­c­u­lar glue de­grad­er that tar­gets a hard-to-drug dri­ver of a type of kid­ney can­cer. Neo­morph has al­so signed re­search deals with Bio­gen, Ab­b­Vie and No­vo Nordisk since emerg­ing from stealth in De­cem­ber 2020 with a $109 mil­lion Se­ries A round. — An­drew Dunn

Click here to continue reading
Endpoints News
2029 Becker Drive; Lawrence, Kansas 66047 USA Privacy and deletion: help@endpointsnews.com
web twitter linkedin