Ver­sant-backed Chi­nook gets a $65M launch round for its dis­cov­ery quest in a resur­gent kid­ney field

Ver­sant is once again step­ping off the beat­en track in biotech to see if they can blaze a trail of their own in a field that has looked too thorny to many in­vestors for years.

The ven­ture group and their part­ners at Ap­ple Tree are bring­ing their lat­est cre­ation out of stealth mode to­day. Born in Ver­sant’s In­cep­tion Sci­ences’ Chi­nook Ther­a­peu­tics is bet­ting that its pre­clin­i­cal take on kid­ney dis­ease can get an ear­ly lead among the com­pa­nies start­ing up in the field.

Head­ed by Er­ic Dob­meier, who left his post as COO of Seat­tle Ge­net­ics to take up the life of a biotech en­tre­pre­neur, Chi­nook is pur­su­ing a pipeline of pre­clin­i­cal pro­grams born in the be­lief that a bet­ter un­der­stand­ing of bi­ol­o­gy, new tech tools and a sup­port­ive FDA of­fer­ing ac­cel­er­at­ed path­ways is all a new recipe for suc­cess in the pur­suit of pre­ci­sion med­i­cines fo­cused on unique pa­tient pop­u­la­tions.

We don’t know what these drugs are, or specif­i­cal­ly what they are tar­get­ing, yet. But Ver­sant and the Chi­nook team be­lieve they will be in the clin­ic in 2021 when it can say a lot more.

For now, they’re hap­py to stay fo­cused on a resur­gent field lit­tered with the corpses of failed drugs.

Jer­el Davis Ver­sant

“It re­minds me of NASH and liv­er dis­ease 4-plus years ago,” says Ver­sant man­ag­ing di­rec­tor Jer­el Davis. Now phar­ma has be­gun set­ting up its own groups to tack­le the field, and he wants in on the ground floor.

Dob­meier has a $65 mil­lion A round and a team of 25 to lead for­ward. You may re­call that Dob­meier’s first biotech gig out of Seat­tle Ge­net­ics was with a com­pa­ny called Sil­ver­back. But they ex­pe­ri­enced an ear­ly set­back, says the biotech ex­ec, and he ex­it­ed the com­pa­ny — join­ing Chi­nook back in April.

Ver­sant and Ap­ple Tree were joined by Sam­sara Bio­Cap­i­tal on the launch round.

The Ver­sant team has made a habit of try­ing to get an ear­ly jump on emerg­ing R&D fields. That strat­e­gy, which in­volves cre­at­ing dis­cov­ery teams in some off-beat places like Van­cou­ver, in­clud­ed their re­gen­er­a­tive stem cell play Blue­Rock, which Bay­er just bought out at a uni­corn val­u­a­tion.

They’re fol­low­ing in the foot­steps of com­pa­nies like Goldfinch, a Third Rock start­up in the class of 2016 that re­cent­ly teamed with Gilead on its ap­proach to kid­ney dis­ease. That heav­i­ly back-end­ed deal helped in­spire Ver­sant to go deep­er. An­oth­er com­pa­ny in the field is Rea­ta, which was once al­lied with Ab­b­Vie — ahead of a clin­i­cal im­plo­sion that they’ve been work­ing to re­cov­er from. 

In a stun­ning set­back, Amarin los­es big patent fight over Vas­cepa IP. And its high-fly­ing stock crash­es to earth

Amarin’s shares $AMRN were blitzed Monday evening, losing billions in value as reports spread that the company had lost its high-profile effort to keep its Vascepa patents protected from generic drugmakers.

Amarin had been fighting to keep key patents under lock and key — and away from generic rivals — for another 10 years, but District Court Judge Miranda Du in Las Vegas ruled against the biotech. She ruled that:
(A)ll the Asserted Claims are invalid as obvious under 35 U.S.C.§ 103. Thus, the Court finds in favor of Defendants on Plaintiff’s remaining infringementclaim, and in their favor on their counterclaims asserting the invalidity of the AssertedClaims under 35 U.S.C. § 103.

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UP­DAT­ED: Have a new drug that promis­es to fight Covid-19? The FDA promis­es fast ac­tion but some de­vel­op­ers aren't hap­py

After providing an emergency approval to use malaria drugs against coronavirus with little actual evidence of their efficacy or safety in that setting, the FDA has already proven that it has set aside the gold standard when it comes to the pandemic. And now regulators have spelled out a new approach to speeding development that promises immediate responses in no uncertain terms — promising a program offering the ultimate high-speed pathway to Covid-19 drug approvals.

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Once fu­ri­ous over No­var­tis’ da­ta ma­nip­u­la­tion scan­dal, the FDA now says it’s noth­ing they need to take ac­tion on

Back in the BP era — Before Pandemic — the FDA ripped Novartis for its decision to keep the agency in the dark about manipulated data used in its application for Zolgensma while its marketing application for the gene therapy was under review.

Civil and criminal sanctions were being discussed, the agency noted in a rare broadside at one of the world’s largest pharma companies. Notable lawmakers cheered the angry regulators on, urging the FDA to make an example of Novartis, which fielded Zolgensma at $2.1 million — the current record for a one-off therapy.

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Covid-19 roundup: GSK, Am­gen tai­lor R&D work to fit the coro­n­avirus age; Doud­na's ge­nomics crew launch­es di­ag­nos­tic lab

You can add Amgen and GSK to the list of deep-pocket drug R&D players who are tailoring their pipeline work to fit a new age of coronavirus.

Following in the footsteps of a lineup of big players like Eli Lilly — which has suspended patient recruitment for drug studies — Amgen and GSK have opted to take a more tailored approach. Amgen is intent on circling the wagons around key studies that are already fully enrolled, and GSK has the red light on new studies while the pandemic plays out.

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The race to de­vel­op Covid-19 drugs and vac­cines is on — here’s what’s hap­pen­ing in the UK

Weeks away from the results of ongoing US and China trials testing its experimental antiviral remdesivir, Gilead is going to trial the failed Ebola drug in a small group of coronavirus patients in England and Scotland. The United Kingdom is also home to a range of other therapeutic efforts, as the pandemic rages on across the globe.

On Tuesday, Southampton, UK-based startup Synairgen kicked off a mid-stage placebo-controlled study testing its experimental drug, SNG001 — an inhaled formulation of interferon-beta-1a — that has previously shown to be safe and effective in improving lung function in asthma patients with a respiratory viral infection in a pair of Phase II trials.

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As­traZeneca says its block­buster Farx­i­ga proved to be a game-chang­er in CKD — wrap­ping PhI­II ear­ly

If the FDA can still hold up its end of the bargain, AstraZeneca is already on a short path to scooping up a cutting-edge win with a likely approval for their SGLT2 drug Farxiga in cutting the risk of heart failure. Now the pharma giant says it can point to solid evidence that the drug — initially restricted to diabetes — also works for chronic kidney disease, potentially adding a blockbuster indication for the franchise.

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‘There was a grow­ing weari­ness’: Rush­ing against a pan­dem­ic clock, As­pen Neu­ro­sciences se­cures $70M Se­ries A

Just before Christmastime, Howard Federoff got a tip from Washington: There was a new virus in China. And this one could be bad.

News report of the virus had not yet appeared. Federoff, a neuroscientist, was briefed because years before, he was vetted as part of a group — he didn’t give a name for the group — to consult for the US government on emerging scientific issues. His day job, though, was CEO of Aspen Neurosciences, a Parkinson’s cell therapy startup that days before had come out of stealth mode and gave word to investors they were hoping to raise $70 million. That, Federoff realized, would be difficult if a pandemic shut down the global economy.

FDA puts pe­di­atric aGVHD drug on pri­or­i­ty re­view lane — will they go vir­tu­al with the ad­comm?

Despite worries about regulatory delays due to new work arrangements under Covid-19, the FDA appears intent to go full speed ahead with its everyday work, not only granting priority review to a stem cell therapy for acute graft versus host disease but also plotting an advisory committee meeting for it.

With a PDUFA date of September 30, the journey of the drug — remestemcel-L, or Ryoncil — could shed light on the agency’s capacity to facilitate drug development unrelated to Covid-19.

Covid-19 roundup: Trump push­es his new fa­vorite, untest­ed drug; CRISPR out­lines crip­pling im­pact of Covid-19

President Trump has a new favorite Covid-19 drug.

After a conversation with Japanese Prime Minister Shinzo Abe, Politico reports, the president is pressuring the FDA to issue emergency use authorization for favipiravir, a flu drug that showed glimpses of success in China but remains unproven and carries a list of worrying side effects. The push comes after a week-plus in which the White House touted a potentially effective but unproven malaria medication despite the concerns of scientific advisors such as NIAID director Anthony Fauci. And Trump ally Rudy Giuliani has been talking up unproven cell therapy efforts on Twitter.

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