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6 February, 2026
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2. Biogen CEO expects Alzheimer's drug Leqembi to sustain growth
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Drew Armstrong
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It looks like IPOs are back. The industry had the best week of new public offerings since 2021, Kyle LaHucik reports today, with $987 million raised.

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

Biotech IPOs are on the come­back trail.

Fi­bro­sis-fo­cused Agomab Ther­a­peu­tics and eye dis­ease com­pa­ny Spy­Glass Phar­ma will go pub­lic on Fri­day in re­spec­tive $200 mil­lion and $150 mil­lion Nas­daq de­buts. Those floats fol­low list­ings ear­li­er this week from two late-stage biotechs: Roger Perl­mut­ter-led Eikon Ther­a­peu­tics and oral Ro­gaine de­vel­op­er Ve­r­a­der­mics.

All told, the four biotechs ex­pect to reel in $987 mil­lion from their pri­vate-to-pub­lic tran­si­tions this week. That makes it the biggest week for biotech IPOs since a nine-list­ing, $1.03 bil­lion week in Ju­ly 2021, ac­cord­ing to an End­points News analy­sis.

The in­dus­try whip­sawed short­ly af­ter that sum­mer's fren­zy. Biotechs un­der­went a four-year down­swing in IPOs, hun­dreds of rounds of lay­offs, count­less pipeline culls, com­pa­ny shut­ter­ings, the rise of Chi­na's bio­med­ical R&D sec­tor, and a par­tic­u­lar­ly bru­tal sev­en-month IPO dry spell in 2025 that end­ed in Sep­tem­ber as the mar­ket be­gan to heat up.

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Chris Viehbacher, Biogen CEO (Suzanne Kreiter/The Boston Globe via Getty Images)
2
by Max Gelman

Bio­gen and Ei­sai's Alzheimer’s drug Leqem­bi ap­pears to have reached some sta­ble growth af­ter a bumpy cou­ple of years.

Leqem­bi gen­er­at­ed $134 mil­lion in fourth-quar­ter sales world­wide in 2025, jump­ing 54% from the pre­vi­ous year and 11% from the third quar­ter. The re­port comes af­ter Ei­sai last year slashed its Leqem­bi sales fore­casts for 2027 in half, cit­ing “de­layed up­take in the US mar­ket.”

Bio­gen CEO Chris Viehbach­er, speak­ing dur­ing his com­pa­ny’s fourth-quar­ter earn­ings call, at­trib­uted the rise to the pro­por­tion of pa­tients who kept tak­ing Leqem­bi af­ter the ini­tial 18-month treat­ment pe­ri­od. About 70% of pa­tients pro­ceed­ed in­to what’s known as the main­te­nance phase, Bio­gen es­ti­mates.

“We don't re­al­ly have clear da­ta about how many pa­tients ac­tu­al­ly go on to main­te­nance, since we re­al­ly on­ly know how many vials we sell,” Viehbach­er said. “But the da­ta that we do have sug­gests that there is this per­sis­ten­cy of about 70%.”

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News Briefing: Quick hits from the biopharma web
3
by ENDPOINTS

⏸️ UniQure paus­es mid- and high-dos­es in Fab­ry gene ther­a­py study: The com­pa­ny re­port­ed that two pa­tients who re­ceived a 4x1013 genome copies per kilo­gram (gc/kg) dose faced grade 3 liv­er en­zyme el­e­va­tions. That comes af­ter the com­pa­ny said last year that a pa­tient who re­ceived the high 6x1013 gc/kg dose al­so ex­pe­ri­enced el­e­vat­ed liv­er en­zyme lev­els. The biotech has paused dos­ing at both dose lev­els, though it is al­so study­ing a low­er 2x1013 gc/kg dose. UniQure re­port­ed at the WORLDSym­po­sium on Fri­day that six of 11 pa­tients treat­ed with its gene ther­a­py no longer re­quire en­zyme re­place­ment ther­a­py. — Lei Lei Wu

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Cell & Gene Day 2026
CGT has fresh momentum from new FDA frameworks and pharma deals, but do the latest advances in science, manufacturing, and regulation actually solve the core challenges? We’re asking the hard questions