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7 April, 2026
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Pre­sent­ing Your Gene Ther­a­py Man­u­fac­tur­ing Plan to In­vestors: What They Ex­pect in 2026 and How to De­liv­er It
top stories
1. Merck got a peek at Terns' leukemia data during its deal talks — and decided to lower its bid by $1B
2. Updated: Gilead continues dealmaking streak with $3.15B Tubulis buy for ADCs
3. ARPA-H selects three academic teams in $100M effort to repair and regrow ailing joints
4.
news briefing
Novo launches high-dose Wegovy in the US; Evotec pressured to list its US unit
5. BioNTech to shutter Singapore HQ after 'comprehensive review'
6. Sanofi bispecific sails through asthma, sinusitis trials, but disappoints in eczema
7. Proposed FDA budget aligns Makary, Trump behind rivaling China biotech
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Drew Armstrong
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New clinical data changed the outlook for Terns’ experimental oncology drug, reducing the biotech’s value to the pharma giant Merck. Read Kyle LaHucik's piece here.

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Drew Armstrong
Executive Editor, Endpoints News
@ArmstrongDrew
1
by Kyle LaHucik

Al­though Mer­ck and Terns Phar­ma­ceu­ti­cals are part of biotech's M&A surge, the $6.7 bil­lion deal did­n't near­ly play out the way ei­ther an­tic­i­pat­ed.

Mer­ck de­cid­ed to sig­nif­i­cant­ly low­er its of­fer for the biotech by about 13% af­ter see­ing up­dat­ed clin­i­cal da­ta that changed the out­look for Tern­s' in­ves­ti­ga­tion­al on­col­o­gy drug, called TERN-701, ac­cord­ing to SEC fil­ings on Tues­day. The doc­u­ments show one of the rare in­stances in which a com­pa­ny drops its of­fer price dur­ing ne­go­ti­a­tions.

The New Jer­sey phar­ma gi­ant will gain ac­cess to an ex­per­i­men­tal chron­ic myeloid leukemia (CML) med­i­cine that could one day com­pete with No­var­tis' block­buster treat­ment Scem­blix. But the da­ta led an­oth­er po­ten­tial ac­quir­er, an un­named "large phar­ma­ceu­ti­cal com­pa­ny" re­ferred to as "Par­ty C," to back out of deal talks. Pri­or to this, a few oth­er com­pa­nies — Par­ties A, B, D and E — had told Terns that they weren't in­ter­est­ed in a deal, ac­cord­ing to the reg­u­la­to­ry pa­per­work.

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Dominik Schumacher, Tubulis CEO (Sven Hoppe/picture alliance via Getty Images)
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by Kyle LaHucik

In its third ac­qui­si­tion of 2026, Gilead is spend­ing $3.15 bil­lion up­front to snag a next-gen­er­a­tion an­ti­body-drug con­ju­gate plat­form from Ger­man start­up Tubu­lis.

The Cal­i­for­nia bio­phar­ma could pay out an­oth­er $1.85 bil­lion down the road to Tubu­lis share­hold­ers if all goes well with the ac­qui­si­tion, which was an­nounced Tues­day morn­ing. Tubu­lis raised a $401 mil­lion Se­ries C last year, had its sights on a po­ten­tial IPO, and re­cruit­ed Roche on­col­o­gy ex­ec­u­tive Charles Fuchs as its chief med­ical of­fi­cer.

“To un­leash the full po­ten­tial of the plat­form, we need a lot of horse­pow­er. We need a lot of re­sources that we cur­rent­ly don’t have,” Tubu­lis CEO Do­minik Schu­mach­er said in an in­ter­view with End­points News. “I’m 100% sure that we could have built lots of those re­sources over time, but we just didn’t want to waste any time to get these med­i­cines to pa­tients.”

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TOP R&D TRENDS IN 2026:
John Carroll’s R&D 15 report is back — and this year, he’s bringing some of the industry’s top research chiefs into the conversation to break down what the data means, what’s shifting, and where biopharma R&D is headed. Join us to find out what comes next.
3
by Ryan Cross

Three aca­d­e­m­ic cen­ters be­lieve they may have dis­cov­ered new ways to heal ag­ing joints. Now the fed­er­al gov­ern­ment is fund­ing clin­i­cal tri­als to test these ex­per­i­men­tal re­gen­er­a­tive med­i­cines in os­teoarthri­tis.

Teams from Duke Uni­ver­si­ty, the Uni­ver­si­ty of Col­orado Boul­der and Co­lum­bia Uni­ver­si­ty could col­lec­tive­ly re­ceive more than $100 mil­lion from the Ad­vanced Re­search Projects Agency for Health (ARPA-H), a fed­er­al agency that funds high-risk and high-re­ward med­ical re­search.

The project, known as Nov­el In­no­va­tions for Tis­sue Re­gen­er­a­tion in Os­teoarthri­tis (NI­TRO), be­gan in 2024 dur­ing the Biden ad­min­is­tra­tion, and some of the fund­ing was al­ready doled out two years ago. While five groups were se­lect­ed for the ini­tial pre­clin­i­cal work, on­ly three will move in­to clin­i­cal stud­ies, which are ex­pect­ed to be­gin with­in 18 months.

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News Briefing: Quick hits from the biopharma web
4
by ENDPOINTS

Plus, news about Ver­tex and Halozyme, Were­wolf, and Re­gen­eron:

No­vo Nordisk launch­es high-dose We­govy in the US: The 7.2 mg in­jectable form of the GLP-1 ag­o­nist is now avail­able in the US to treat obe­si­ty pa­tients via tele­health providers in­clud­ing No­vo’s own Novo­Care Phar­ma­cy, as well as brick-and-mor­tar phar­ma­cies. It will cost $399 per month for cash-pay cus­tomers, but pa­tients will work their way up to this lev­el from low­er, cheap­er dos­es. The new dose was ap­proved swift­ly via the Com­mis­sion­er’s Na­tion­al Pri­or­i­ty Vouch­er pro­gram in March, based on piv­otal tri­al da­ta show­ing weight loss of about 19% at 72 weeks, us­ing an in­tent-to-treat analy­sis. — Eliz­a­beth Cairns