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16 January, 2025
A year of contrasts: biotech investment soars, exit linger
New SVB report reveals a banner year for investments in biotech.
sponsored by Silicon Valley Bank
top stories
1.
in focus
Broad Institute paper offers potential new framework for treating Huntington’s disease
2. FDA rejects Atara's cell therapy for rare transplant complication, stock craters
3. Vaccine patch startup collects an additional $16M to Series A
4.
news briefing
Boehringer's schizophrenia asset fails Phase 3; GSK buys organoid biotech
5.
bioregnum
A mixed year for deals and dollars left biotech execs hungry for a better 2025
6. Eli Lilly's Omvoh earns FDA approval for Crohn's disease
7. FDA explains why it rejected Vanda's stomach drug in late 2024
more stories
 
 
 
Max Gelman
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Thanks to everyone who read our coverage and came out to our events at JPM this week! If you missed anything, be sure to read the live blogs our reporters put together over the last three days.

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Max Gelman
Senior Editor, Endpoints News
@MaxGelman
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Credit: Shutterstock
Endpoints In Focus
1
by Max Gelman

Most clin­i­cal tri­als for Hunt­ing­ton’s dis­ease have run aground in the last few years, but aca­d­e­m­ic re­searchers haven’t been dis­suad­ed from try­ing to shift how the rare ge­net­ic dis­or­der is un­der­stood.

A hand­ful of pa­pers re­leased in the last 12 months sug­gest those shifts are com­ing soon­er rather than lat­er. The lat­est sci­en­tif­ic study, pub­lished in Cell on Thurs­day, comes from re­searchers at the Broad In­sti­tute of MIT and Har­vard. They claim pre­vi­ous re­search may have been look­ing at the dis­ease the wrong way and of­fer a po­ten­tial new frame­work for treat­ments.

Led by Steve Mc­Car­roll and Sabi­na Berret­ta, the group looked at post­mortem brain tis­sue of Hunt­ing­ton’s pa­tients and com­pared it to tis­sue from in­di­vid­u­als with­out Hunt­ing­ton’s, aim­ing to see how a spe­cif­ic DNA mu­ta­tion in­flu­ences the dis­ease’s pathol­o­gy. They as­sert, con­trary to ear­ly as­sump­tions, that Hunt­ing­ton’s pa­tients don’t slow­ly de­te­ri­o­rate.

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2
by Lei Lei Wu, Max Gelman

US reg­u­la­tors have re­ject­ed a T cell ther­a­py for a rare and se­ri­ous trans­plant com­pli­ca­tion re­lat­ed to Ep­stein-Barr virus from Atara Bio­ther­a­peu­tics and Pierre Fab­re.

The ther­a­py, known as tab­ele­cleu­cel or tab-cel, was turned away af­ter the FDA in­spect­ed a third-par­ty man­u­fac­tur­ing site, Atara said in a Thurs­day press re­lease. FDA's re­jec­tion let­ter "did not iden­ti­fy any de­fi­cien­cies" re­lat­ed to the man­u­fac­tur­ing of the ther­a­py it­self, nor any con­cerns over ef­fi­ca­cy or safe­ty da­ta, Atara said. Ad­di­tion­al­ly, it will not be re­quired to run an­oth­er clin­i­cal tri­al.

Atara's stock price ATRA fell more than 45% on Thurs­day morn­ing.

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3
by Anna Brown

Vac­cine tech com­pa­ny Mi­cron Bio­med­ical has start­ed 2025 on a pos­i­tive note, rais­ing over $16 mil­lion in a Se­ries A ex­ten­sion round.

The fund­ing will be used to man­u­fac­ture its vac­cine “but­ton” tech­nol­o­gy as it gears up for a po­ten­tial com­mer­cial launch in 2027, CEO Steve Da­mon told End­points News. The com­pa­ny’s tech is a small coin-sized but­ton con­tain­