Af­ter sell­ing to Genen­tech, the old Je­cure team is back at an RNA-fo­cused start­up — and more en­thu­si­as­tic than ever

When Genen­tech swooped in to buy NASH-fo­cused Je­cure Ther­a­peu­tics back in 2018, a hand­ful of the start­up’s ex­ec­u­tives weren’t quite ready to dis­perse.

It had been just three years since Je­cure launched with a pre­clin­i­cal port­fo­lio of NL­RP3 in­hibitors — and the takeover came soon­er than any­one, in­clud­ing CEO Jeff Stafford, had ex­pect­ed. So he got talk­ing with James Veal and Gretchen Bain, two se­r­i­al en­tre­pre­neurs in charge of Je­cure’s R&D.

“We want­ed to do some­thing to­geth­er again,” Stafford told End­points News. “All of us share a high en­thu­si­asm for ear­ly stage drug dis­cov­ery, and had some ideas.”

Jeff Stafford

A year lat­er, they launched 858 Ther­a­peu­tics — named af­ter the San Diego area code — to fo­cus on the bur­geon­ing field of RNA mod­u­la­tion and the role it plays in can­cer. Right away, they snapped up Gotham Ther­a­peu­tics, a New York-based start­up that was cre­at­ing med­i­cines to drug key pro­teins that mod­u­late mR­NA, for an undis­closed amount.

And on Tues­day, they emerged from stealth mode with a $60 mil­lion Se­ries A round led by Ver­sant Ven­tures. NEA, Cor­morant As­set Man­age­ment and Lo­gos Cap­i­tal chipped in­to the round.

“We just found that space to be in­cred­i­bly dy­nam­ic where there have been, over the last few years, just a whole host of break­through dis­cov­er­ies,” Ver­sant part­ner Car­lo Riz­zu­to said.

Car­lo Riz­zu­to

While the in­dus­try was ini­tial­ly laser-fo­cused on mod­i­fy­ing DNA, ev­i­dence be­gan pil­ing up years ago that RNA mod­i­fi­ca­tions could help de­ter­mine to which de­gree genes are trans­lat­ed in­to pro­teins. The mod­i­fi­ca­tions play a big role in some can­cers — but un­til re­cent­ly, sci­en­tists have strug­gled to ad­dress those tar­gets due to a dearth of as­says and chal­lenges in cre­at­ing chem­i­cal mat­ter with drug-like prop­er­ties, Stafford said.

858’s plat­form re­volves around “spe­cial­ized know-how and spe­cial­ized as­says,” ac­cord­ing to Stafford. The Se­ries A mon­ey should be enough to get the team in­to the clin­ic by 2023 — but the CEO was care­ful not to dis­close the team’s tar­gets just yet. He says the com­pa­ny should be able to tack­le three to five pro­grams at a giv­en time.

Veal and Bain are on board as CSO and VP of bi­ol­o­gy, re­spec­tive­ly — the same roles they held at Je­cure. All three ex­ecs have ex­pe­ri­ence at Ver­sant-backed biotechs, in­clud­ing Quan­ti­cel and Ami­ra Phar­ma­ceu­ti­cals, which were bought by Cel­gene and Bris­tol My­ers Squibb, re­spec­tive­ly.

Stafford says he’s look­ing to ex­pand the 25-per­son team to 40 in the next 18 months, with head­quar­ters in San Diego and op­er­a­tions in New York.

“(It’s) I think very rare in this busi­ness to get to work with the same team over mul­ti­ple suc­cess­ful com­pa­nies,” Riz­zu­to said. “There are not many, you know, three-times suc­cess­ful teams that are do­ing their fourth com­pa­ny and so I think that’s a very clear point of dif­fer­en­ti­a­tion.”

Bio­mark­er 'roadmap­s' and the fu­ture of can­cer R&D; Cur­tain rais­es on #AS­CO22; Pfiz­er, No­var­tis tack­le drug ac­cess; and more

Welcome back to Endpoints Weekly, your review of the week’s top biopharma headlines. Want this in your inbox every Saturday morning? Current Endpoints readers can visit their reader profile to add Endpoints Weekly. New to Endpoints? Sign up here.

While this was not a week for earth-shattering news, there were certainly a lot of interesting tidbits. If you found this recap helpful, please recommend it to your friends and colleagues. We’ll see you on the other side of the long weekend.

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Keep­ing pres­sure on Am­gen, Mi­rati draws mixed re­views on lat­est cut of KRAS da­ta

As the close runner-up to Amgen’s Lumakras in the KRAS race, any data cut from Mirati’s adagrasib continues to draw scrutiny from analysts. And the latest batch of numbers from ASCO is a decidedly mixed bag.

While a quick comparison suggests that adagrasib spurred slightly more responses and led to a longer overall survival than Lumakras among a group of non-small cell lung cancer patients, its duration of response appears shorter and the safety profile continues to spark concern.

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Ann is one of ViiV Healthcare's newest spokespeople as the retired school administrator speaks up about her HIV status.

GSK's Vi­iV de­buts next evo­lu­tion in HIV med Dova­to cam­paign with new spokes­peo­ple and new mes­sage

When Ann saw the first TV commercials for HIV medicine Dovato, she didn’t see herself represented. So the 74-year-old retired school administrator who’s been living with HIV since 1998, reached out to GSK’s ViiV Healthcare and asked why not?

Now Ann is one of three people starring in ViiV’s latest Dovato campaign called “Detect This.” The next-step evolution in the branded campaign plays on the word “detect” — often used in describing HIV status under control as undetectable — but in this case, uses the word as a directive for people to understand they can use fewer medicines.

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Tran­si­tion to new Eu­ro­pean clin­i­cal tri­als in­fo sys­tem starts slow­ly

At the end of January, the European Medicines Agency officially launched its new clinical trials info system (CTIS), although the migration to the new platform has only really just begun, and sponsors have until the end of January 2023 before all initial trial applications must be submitted through CTIS.

Overall, 56 clinical trial applications have been submitted in CTIS during the first 3 months since the launch of the system on Jan. 31, according to new data posted by the EMA. By comparison, about 4,000 new trials are authorized each year across Europe.

Switzer­land to de­stroy over 600,000 ex­pired dos­es of Mod­er­na Covid vac­cine

As concerns related to uptake and distribution continue to linger, Switzerland is among the first countries that plans to destroy hundreds of thousands of expired and unused Covid-19 vaccine doses.

The European country said it plans to destroy more than 600,000 doses of Moderna’s Spikevax Covid-19 vaccine as the doses have reached their expiration date.

However, Moderna CEO Stéphane Bancel told the World Economic Forum in Davos, Switzerland that he’s in the process of throwing 30 million doses in the garbage, exclaiming, “We have a big demand problem.”

Nassim Usman, Catalyst Biosciences CEO

Af­ter $60M Ver­tex deal, group of Cat­a­lyst share­hold­ers claims biotech could’ve sold as­sets three years ago

Catalyst Biosciences was down to five employees in March, and the biotech needed to do something after two rounds of layoffs, a nixed collaboration and a culling of its hemophilia program.

In came Vertex, with $60 million to buy up the South San Francisco biotech’s preclinical complement drugs, which target the system that bridges the body’s innate and adaptive immune response and a class most known for Ultomiris and Soliris. The deal includes CB 2782-PEG, the dry AMD drug that Biogen no longer wanted in March.

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Lina Khan, FTC chair (Graeme Jennings/Pool via AP Images)

Pile-on over PBMs con­tin­ues with FTC com­ments and a new bi­par­ti­san Sen­ate bill

More than 500 stakeholders sent comments to the FTC on whether the commission should look further into pharma middlemen, known as PBMs, with many of the commenters calling for more federal oversight.

Similar to the critical open comment period in a deadlocked FTC session last February, pharmacies and pharmacy groups are continuing to call out the lack of transparency among the top 3 PBMs, which control about 80% of the market.

Pharma brands are losing their shine with US consumers who are now thinking about the economy and inflation instead of Covid. (Credit: Shutterstock)

Phar­ma brands fade in an­nu­al Har­ris con­sumer vis­i­bil­i­ty poll: Mod­er­na drops off and Pfiz­er dips

As Covid-19 concerns are fading in the US, so is biopharma visibility. The annual Axios Harris Poll survey to determine and rank the 100 most top-of-mind brands in the US finds Moderna, which was No. 3 last year, not on the list at all for 2022, and Pfizer sinking 37 spots.

However, it’s not that Moderna or Pfizer did anything wrong, it’s just that Americans have moved on to other worries beyond Covid.

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HHS Secretary Xavier Becerra (Jacquelyn Martin/AP Images)

HHS fin­ish­es off Trump-era rule that would've erased ba­sic FDA regs with­out fre­quent re­views

HHS on Thursday finalized its decision to withdraw a rule, proposed just before former President Donald Trump left office, that would’ve caused thousands of HHS and FDA regulations to automatically expire if they weren’t reviewed within two years, and every 10 years thereafter.

The decision follows the filing of a lawsuit last March, in which several nonprofits alleged that the outgoing administration planted “a ticking timebomb” for HHS, essentially forcing it to devote an enormous amount of resources to the unprecedented and infeasible task of reviewing thousands of regulations regularly.