In­Car­da grabs a $42M round to back PoC study for their in­haled car­dio drug

San Fran­cis­co-based In­Car­da Ther­a­peu­tics is tak­ing a big step for­ward to­day, un­veil­ing a $42 mil­lion B round af­ter get­ting the com­pa­ny launched on a shoe­string bud­get. The new mon­ey from a promi­nent group of in­vestors puts the com­pa­ny on track to ob­tain proof-of-con­cept da­ta for a new in­haled drug to treat in­ci­dents of parox­ys­mal atri­al fib­ril­la­tion. And they have some am­bi­tious plans to even­tu­al­ly take the tech out of a hos­pi­tal set­ting and in­to the streets.

Grace Colón

Their drug is an in­haled ver­sion of an old oral drug called fle­cainide, which has been sold out­side the US to treat PAF. The 15-mem­ber staff at In­Car­da is fo­cused on a rapid re­sponse to acute in­ci­dents, po­ten­tial­ly re­duc­ing the num­ber of car­dio events ex­pe­ri­enced by these pa­tients.

The mon­ey gives In­Car­da enough cash for the Phase II, cov­er­ing about 100 pa­tients with da­ta due at the end of H1 next year. Then they plan to push in­to Phase III with a few hun­dred pa­tients in search of an FDA OK for use in a su­per­vised set­ting.

“That’s the first in­di­ca­tion — a hos­pi­tal or ur­gent care set­ting,” where pa­tients can be su­per­vised, says CEO Grace Colón. “The big vi­sion is some­thing that pa­tients can use to treat them­selves.” Armed with neb­u­liz­ers and a portable com­pres­sor, this is some­thing the com­pa­ny be­lieves can be used by pa­tients to stop an at­tack of PAF in 3 to 5 min­utes.

“The oral drug was nev­er stud­ied for acute con­ver­sion,” she adds, with a small physi­cian-led study for acute care, “and it works fair­ly well 40-50% for that. It takes an hour or 2 for that con­ver­sion to be achieved.”

Colón cred­its Nek­tar vet John Pat­ton and a few oth­ers for bring­ing the orig­i­nal com­pa­ny to­geth­er and fo­cus­ing it on the IP avail­able. Pat­ton “hired me when the com­pa­ny had no mon­ey,” she re­calls rue­ful­ly. But with the help of an­gel mon­ey from the “friends and fam­i­ly” class, they got their first few hun­dred thou­sand in place for a launch, fol­lowed by a $5 mil­lion A round to get things boot­ed up.

This new syn­di­cate brings in some heavy hit­ters.

Sofinno­va Ven­tures and Health­Cap led the round, which al­so in­clud­ed new in­vestor Deer­field Man­age­ment and ex­ist­ing in­vestors Morn­ing­side Ven­ture and As­set Man­age­ment Ven­tures.

It’s fi­nal­ly over: Bio­gen, Ei­sai scrap big Alzheimer’s PhI­I­Is af­ter a pre­dictable BACE cat­a­stro­phe rais­es safe­ty fears

Months after analysts and investors called on Biogen and Eisai to scrap their BACE drug for Alzheimer’s and move on in the wake of a string of late-stage failures and rising safety fears, the partners have called it quits. And they said they were dropping the drug — elenbecestat — after the independent monitoring board raised concerns about…safety.

We don’t know exactly what researchers found in this latest catastrophe, but the companies noted in their release that investigators had determined that the drug was flunking the risk/benefit analysis.

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Pur­due Phar­ma files for bank­rupt­cy as first step in $10B opi­oid set­tle­ment

It’s settled. Purdue Pharma has filed for bankruptcy as part of a deal that would see the OxyContin maker hand over $10 billion in cash and other contributions to mitigate the opioid crisis — without acknowledging any wrongdoing in the protracted epidemic that’s resulted in hundreds of thousands of deaths.

The announcement came two weeks after news of a proposed settlement surfaced and largely confirm what’s already been reported.

Deborah Dunsire. Lundbeck

Deb­o­rah Dun­sire is pay­ing $2B for a chance to leap di­rect­ly in­to a block­buster show­down with a few of the world's biggest phar­ma gi­ants

A year after taking the reins as CEO of Lundbeck, Deborah Dunsire is making a bold bid to beef up the Danish biotech’s portfolio of drugs in what will likely be a direct leap into an intense rivalry with a group of giants now carving up a growing market for new migraine drugs.

Bright and early European time the company announced that it will pay up to about $2 billion to buy Alder, a little biotech that is far along the path in developing a quarterly IV formulation for a CGRP drug aimed at cutting back the number of crippling migraines patients experience each month.

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Lisa M. DeAngelis, MSKCC

MSK picks brain can­cer ex­pert Lisa DeAn­ge­lis as its next CMO — fol­low­ing José Basel­ga’s con­tro­ver­sial ex­it

It’s official. Memorial Sloan Kettering has picked a brain cancer expert as its new physician-in-chief and CMO, replacing José Baselga, who left under a cloud after being singled out by The New York Times and ProPublica for failing to properly air his lucrative industry ties.

His replacement, who now will be in charge of MSK’s cutting-edge research work as well as the cancer care delivered by hundreds of practitioners, is Lisa M. DeAngelis. DeAngelis had been chair of the neurology department and co-founder of MSK’s brain tumor center and was moved in to the acting CMO role in the wake of Baselga’s departure.

Penn team adapts CAR-T tech, reengi­neer­ing mouse cells to treat car­diac fi­bro­sis

After establishing itself as one of the pioneer research centers in the world for CAR-T cancer therapies, creating new attack vehicles to eradicate cancer cells, a team at Penn Medicine has begun the tricky transition of using the basic technology for heart repair work.

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Tal Zaks. Moderna

The mR­NA uni­corn Mod­er­na has more ear­ly-stage hu­man da­ta it wants to show off — reach­ing new peaks in prov­ing the po­ten­tial

The whole messenger RNA field has attracted billions of dollars in public and private investor cash gambled on the prospect of getting in on the ground floor. And this morning Boston-based Moderna, one of the leaders in the field, wants to show off a few more of the cards it has to play to prove to you that they’re really in the game.

The whole hand, of course, has yet to be dealt. And there’s no telling who gets to walk with a share of the pot. But any cards on display at this point — especially after being accused of keeping its deck under lock and key — will attract plenty of attention from some very wary, and wired, observers.

“In terms of the complexity and unmet need,” says Tal Zaks, the chief medical officer, “this is peak for what we’ve accomplished.”

Moderna has two Phase I studies it wants to talk about now.

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It's not per­fect, but it's a good start: FDA pan­elists large­ly en­dorse Aim­mune's peanut al­ler­gy ther­a­py

Two days after a fairly benign review from FDA staff, an independent panel of experts largely endorsed the efficacy and safety of Aimmune’s peanut allergy therapy, laying the groundwork for approval with a risk evaluation and mitigation strategy (REMS).

Traditionally, peanut allergies are managed by avoidance, but the threat of accidental exposure cannot be nullified. Some allergists have devised a way to dose patients off-label with peanut protein derived from supermarket products to wean them off their allergies. But the idea behind Aimmune’s product was to standardize the peanut protein, and track the process of desensitization — so when accidental exposure in the real world invariably occurs, patients are less likely to experience a life-threatening allergic reaction.

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Rit­ter bombs fi­nal PhI­II for sole lac­tose in­tol­er­ance drug — shares plum­met

More than two years ago Ritter Pharmaceuticals managed to find enough silver lining in its Phase IIb/III study — after missing the top-line mark — to propel its lactose intolerance toward a confirmatory trial. But as it turned out, the enthusiasm only set the biotech and its investors up to be sorely disappointed.

This time around there’s little left to salvage. Not only did RP-G28 fail to beat placebo in reducing lactose intolerance symptoms, patients in the treatment group actually averaged a smaller improvement. On a composite score measuring symptoms like abdominal pain, cramping, bloating and gas, patients given the drug had a mean reduction of 3.159 while the placebo cohort saw a 3.420 drop on average (one-sided p-value = 0.0106).

Ear­ly snap­shot of Ad­verum's eye gene ther­a­py sparks con­cern about vi­sion loss

An early-stage update on Adverum Biotechnologies’ intravitreal gene therapy has triggered investor concern, after patients with wet age-related macular degeneration (AMD) saw their vision deteriorate, despite signs that the treatment is improving retinal anatomy.

Adverum, on Wednesday, unveiled 24-week data from the OPTIC trial of its experimental therapy, ADVM-022, in six patients who have been administered with one dose of the therapy. On average, patients in the trial had severe disease with an average of 6.2 anti-VEGF injections in the eight months prior to screening and an average annualized injection frequency of 9.3 injections.