As Shkre­li at­tor­ney Greebel heads to his own prison cell, the bad boy of biotech is still skew­er­ing en­e­mies in new blog

Late last week Evan Greebel was sen­tenced to 18 months in prison for his role in Mar­tin Shkre­li’s scheme to de­fraud in­vestors. And he’s be­ing forced to pay more than $10 mil­lion in resti­tu­tion to Retrophin, a biotech Shkre­li had found­ed which fed­er­al pros­e­cu­tors would go on to al­lege was turned in­to Shkre­li’s own per­son­al pig­gy­bank as he sought to pump up the stock and re­pay those same in­vestors he was con­vict­ed of ly­ing to.

“I will re­gret every day of my life the day I met Mar­tin Shkre­li,” Greebel told the court, ac­cord­ing to the Wall Street Jour­nal. And he’ll have lots of time to think on that con­nec­tion.

Shkre­li, now serv­ing a 7-year sen­tence for fraud at the low-se­cu­ri­ty fed­er­al cor­rec­tion­al in­sti­tute at Fort Dix, will have to spend much more time be­hind bars. But he’s al­ready found an out­let for en­ter­tain­ing a much larg­er au­di­ence than he can find in prison.

Shkre­li’s been post­ing a reg­u­lar blog piece at mar­tin­shkre­, and it’s giv­en the “most hat­ed man in Amer­i­ca” with the no­to­ri­ous smirk a fo­rum while of­fer­ing peo­ple a chance to take their own shots back — or of­fer up some cheers from the dis­tant side­lines of the pen­i­ten­tiary sys­tem.

This is a much tamer Shkre­li than the bad boy of biotech who was re­peat­ed­ly boot­ed from Twit­ter for stalk­ing a fe­male jour­nal­ist with creepy mes­sages, or who once got a kick out of send­ing me an ob­scen­i­ty-laced rap song and added email warn­ings about my “loss-of-func­tion mu­ta­tion – do not re­pro­duce” and oth­er per­ceived short­com­ings.

In or­der to avoid ril­ing prison au­thor­i­ties, who con­trol these things, Shkre­li is of­fer­ing up a steady stream of toned down seg­ments rang­ing from in­vest­ment ad­vice, both long and short, to his list of fa­vorite busi­ness books, the oc­ca­sion­al jibe at Hillary Clin­ton — “un­trust­wor­thy par­a­site” — and in­struc­tions for send­ing him mail.

He still en­joys tar­get­ing peo­ple, aside from Clin­ton, but the lan­guage is sig­nif­i­cant­ly less provoca­tive. One ex­am­ple:

Sarah Jeong join­ing the New York Times is a dis­grace.

And there’s lots of time to read at Fort Dix, with no short­age of read­ing ma­te­ri­als.

I’ve re­ceived around 500 books by mail since I en­tered the prison sys­tem. There is a Twi­light Zone episode, “Time Enough At Last” (I think that’s what it is called!), that sum­ma­rizes my feel­ings on hav­ing a lot of time to read. It’s a joy, but I don’t ex­act­ly have the shelf space. I prob­a­bly have around 50 books here at Fort Dix.

Shkre­li has about 6 more years of blog posts com­ing, if he serves the full time. That should be about 300 or so more blog posts. It’s un­like­ly he’ll tire of it.

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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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.

Alex Ar­faei trades his an­a­lyst's post for a new role as biotech VC; Sanofi vet heads to Vi­for

Too often, Alex Arfaei arrived too late. 

An analyst at BMO Capital Markets, he’d meet with biotech or pharmaceutical heads for their IPO or secondary funding and his brain, trained on a biology degree and six years at Merck and Endo, would spring with questions: Why this biomarker? Why this design? Why not this endpoint? Not that he could do anything about it. These execs were coming for clinical money; their decisions had been made and finalized long ago.

Arde­lyx bags its first FDA OK for IBS, set­ting up a show­down with Al­ler­gan, Iron­wood

In the first of what it hopes will be a couple of major regulatory milestones for its new drug, Ardelyx has bagged an FDA approval to market Ibsrela (tenapanor) for irritable bowel syndrome.

The drug’s first application will be for IBS with constipation (IBS-C), inhibiting sodium-hydrogen exchanger NHE3 in the GI tract in such a way as to increase bowel movements and decrease abdominal pain. This comes on the heels of two successful Phase III trials.