A judge or­ders Mar­tin Shkre­li to zip it -- af­ter Twit­ter shuts down his lat­est on­line ac­count

A fed­er­al judge told Mar­tin Shkre­li to shut up about his se­cu­ri­ties fraud case while he’s in and around the cour­t­house. And just be­fore lawyers ar­gued over a prospec­tive gag or­der, Twit­ter shut and locked the back door Shkre­li had ev­i­dent­ly found to worm his way back on­to the so­cial me­dia plat­form.

Ear­ly this morn­ing I no­ticed that@BLM­Bro is now miss­ing in ac­tion, sus­pend­ed by the pow­ers that be at Twit­ter, which had banned Shkre­li af­ter he be­gan ha­rass­ing a free­lance jour­nal­ist.

Over the week­end, The New York Times iden­ti­fied @BLM­Bro as his lat­est Twit­ter han­dle, where he has en­joyed roast­ing crit­ics and be­ing praised by his fans for his opin­ions on vir­tu­al­ly every­thing. The 34-year-old is on tri­al for de­fraud­ing in­vestors, but he’s far bet­ter known for jack­ing the price of a gener­ic drug by more than 5000%.

Shkre­li man­aged to sur­prise just about every­one by am­bling in­to the press area on Fri­day to chat with re­porters cov­er­ing his tri­al, slam­ming the pros­e­cu­tors as “ju­nior var­si­ty,” mock­ing the first wit­ness for the pros­e­cu­tion and shred­ding the air of qui­et that the de­fense ex­pects from their clients dur­ing the course of a tri­al. Pros­e­cu­tors want it to stop, de­mand­ing that the de­fen­dant be gagged — some­thing that no one has yet man­aged to do.

“Un­for­tu­nate­ly, de­spite the as­sur­ances of de­fense coun­sel pri­or to tri­al—as well as ef­forts by de­fense coun­sel to con­trol Shkre­li—once the ju­ry was se­lect­ed and em­pan­eled, Shkre­li em­barked on a cam­paign of dis­rup­tion by com­ment­ing on tri­al ev­i­dence and wit­ness­es to the press and on so­cial me­dia, and by mak­ing a spec­ta­cle of him­self and the tri­al di­rect­ly on the cour­t­house grounds,” pros­e­cu­tors ar­gued, ac­cord­ing to The Dai­ly Beast.

Shkre­li’s at­tor­ney al­ready has pushed back against the gag or­der, ac­cord­ing to CN­BC, ar­gu­ing that the ex-Retrophin CEO isn’t try­ing to harm the in­tegri­ty of the pro­ceed­ings.

“Rather his com­ments are the some­what nat­ur­al, though un­for­tu­nate, con­se­quence of a young man with a demon­strat­ed his­to­ry of sig­nif­i­cant anx­i­ety be­ing at the cen­ter of a supreme­ly dif­fi­cult time in his life,” Ben­jamin Braf­man wrote, ac­cord­ing to CN­BC. Shkre­li feels he’s been un­fair­ly tar­get­ed by the feds, adds the at­tor­ney, and jour­nal­ists fre­quent­ly fo­cus on the neg­a­tive when it comes to their cov­er­age. “Hav­ing said that, we al­so note that Mr. Shkre­li is un­der enor­mous pres­sure that is com­pound­ed by his clear­ly frail emo­tion­al state.”

Pros­e­cu­tors al­so re­vealed this morn­ing that Shkre­li’s de­fense team had asked about a plea deal, the lat­est in a se­ries of con­tra­dic­tions Shkre­li has faced in the court­room.

Shkre­li, for his part, still rou­tine­ly takes to live streams and any oth­er pub­lic stages to ex­pound on the case, in­vest­ing, news cov­er­age of his tri­al and more.

But Twit­ter is once again off lim­its.

For now.

Hal Barron, GSK

Break­ing the death spi­ral: Hal Bar­ron talks about trans­form­ing the mori­bund R&D cul­ture at GSK in a crit­i­cal year for the late-stage pipeline

Just ahead of GlaxoSmithKline’s Q2 update on Wednesday, science chief Hal Barron is making the rounds to talk up the pharma giant’s late-stage strategy as the top execs continue to woo back a deeply skeptical investor group while pushing through a whole new R&D culture.

And that’s not easy, Barron is quick to note. He told the Financial Times:

I think that culture, to some extent, is as hard, in fact even harder, than doing the science.

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Aca­dia is mak­ing the best of it, but their lat­est PhI­II Nu­plazid study is a bust

Acadia’s late-stage program to widen the commercial prospects for Nuplazid has hit a wall. The biotech reported that their Phase III ENHANCE trial flat failed. And while they $ACAD did their best to cherry pick positive data wherever they can be found, this is a clear setback for the biotech.

With close to 400 patients enrolled, researchers said the drug flunked the primary endpoint as an adjunctive therapy for patients with an inadequate response to antipsychotic therapy. The p-value was an ugly 0.0940 on the Positive and Negative Syndrome Scale, which the company called out as a positive trend.

Their shares slid 12% on the news, good for a $426 million hit on a $3.7 billion market cap at close.

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Some Big Phar­mas stepped up their game on da­ta trans­paren­cy — but which flunked the test?

The nonprofit Bioethics International has come out with their latest scorecard on data transparency among the big biopharmas in the industry — flagging a few standouts while spotlighting some laggards who are continuing to underperform.

Now in its third year, the nonprofit created a new set of standards with Yale School of Medicine and Stanford Law School to evaluate the track record on trial registration, results reporting, publication and data-sharing practice.

Busy Gilead crew throws strug­gling biotech a life­line, with some cash up­front and hun­dreds of mil­lions in biobucks for HIV deal

Durect $DRRX got a badly needed shot in the arm Monday morning as Gilead’s busy BD team lined up access to its extended-release platform tech for HIV and hepatitis B.

Gilead, a leader in the HIV sector, is paying a modest $25 million in cash for the right to jump on the platform at Durect, which has been using its technology to come up with an extended-release version of bupivacaine. The FDA rejected that in 2014, but Durect has been working on a comeback.

In­tec blitzed by PhI­II flop as lead pro­gram fails to beat Mer­ck­'s stan­dard com­bo for Parkin­son’s

Intec Pharma’s $NTEC lead drug slammed into a brick wall Monday morning. The small-cap Israeli biotech reported that its lead program — coming off a platform designed to produce a safer, more effective oral drug for Parkinson’s — failed the Phase III at the primary endpoint.

Researchers at Intec, which has already seen its share price collapse over the past few months, says that its Accordion Pill-Carbidopa/Levodopa failed to prove superior to Sinemet in reducing daily ‘off’ time. 

Cel­gene racks up third Ote­zla ap­proval, heat­ing up talks about who Bris­tol-My­ers will sell to

Whoever is taking Otezla off Bristol-Myers Squibb’s hands will have one more revenue stream to boast.

The drug — a rising star in Celgene’s pipeline that generated global sales of $1.6 billion last year — is now OK’d to treat oral ulcers associated with Behçet’s disease, a common symptom for a rare inflammatory disorder. This marks the third FDA approval for the PDE4 inhibitor since 2014, when it was greenlighted for plaque psoriasis and psoriatic arthritis.

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Francesco De Rubertis

Medicxi is rolling out its biggest fund ever to back Eu­rope's top 'sci­en­tists with strange ideas'

Francesco De Rubertis built Medicxi to be the kind of biotech venture player he would have liked to have known back when he was a full time scientist.

“When I was a scientist 20 years ago I would have loved Medicxi,’ the co-founder tells me. It’s the kind of place run by and for investigators, what the Medicxi partner calls “scientists with strange ideas — a platform for the drug hunter and scientific entrepreneur. That’s what I wanted when I was a scientist.”

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Af­ter a decade, Vi­iV CSO John Pot­tage says it's time to step down — and he's hand­ing the job to long­time col­league Kim Smith

ViiV Healthcare has always been something unique in the global drug industry.

Owned by GlaxoSmithKline and Pfizer — with GSK in the lead as majority owner — it was created 10 years ago in a time of deep turmoil for the field as something independent of the pharma giants, but with access to lots of infrastructural support on demand. While R&D at the mother ship inside GSK was souring, a razor-focused ViiV provided a rare bright spot, challenging Gilead on a lucrative front in delivering new combinations that require fewer therapies with a more easily tolerated regimen.

They kept a massive number of people alive who would otherwise have been facing a death sentence. And they made money.

And throughout, John Pottage has been the chief scientific and chief medical officer.

Until now.

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Vlad Coric (Biohaven)

In an­oth­er dis­ap­point­ment for in­vestors, FDA slaps down Bio­haven’s re­vised ver­sion of an old ALS drug

Biohaven is at risk of making a habit of disappointing its investors.

Late Friday the biotech $BHVN reported that the FDA had rejected its application for riluzole, an old drug that they had made over into a sublingual formulation that dissolves under the tongue. According to Biohaven, the FDA had a problem with the active ingredient used in a bioequivalence study back in 2017, which they got from the Canadian drugmaker Apotex.

Apotex, though, has been a disaster ground. The manufacturer voluntarily yanked the ANDAs on 31 drugs — in late 2017 — after the FDA came across serious manufacturing deficiencies at their plants in India. A few days ago, the FDA made it official.

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