UniQure CEO Soland makes a quick ex­it as ex­ecs ham­mer out a new strat­e­gy

Dan Soland

Nine months af­ter land­ing a new job as CEO of the Dutch gene ther­a­py biotech uniQure, Dan Soland abrupt­ly quit on Thurs­day, say­ing the un­ex­pect­ed move was due “sole­ly” to fam­i­ly rea­sons. And the com­pa­ny says it doesn’t plan on re­plac­ing him im­me­di­ate­ly, pre­fer­ring to wait un­til af­ter it im­ple­ments a new cor­po­rate strat­e­gy now in the works.

CFO Matthew Ka­pus­ta will now take the helm as in­ter­im CEO, with for­mer pres­i­dent Philip Ast­ley-Sparke step­ping up as chair­man. In a state­ment, Ast­ley-Sparke praised Ka­pus­ta for his work “guid­ing an on­go­ing, com­pre­hen­sive strate­gic plan­ning process.”

I queried Ast­ley-Sparke — the CEO of BioVex when Am­gen bought it for $425 mil­lion up front, plus mile­stones — on what that cor­po­rate strat­e­gy will fo­cus on, but didn’t hear back im­me­di­ate­ly.

In­ter­im CEO Matt Ka­pus­ta

The change­up comes a few months af­ter uniQure fared poor­ly in the lat­est beau­ty con­test among the gene ther­a­pies be­ing de­vel­oped for he­mo­phil­ia B. A crowd­ed field, Spark Ther­a­peu­tics $ONCE drew praise for achiev­ing 27% to 35% Fac­tor IX (FIX) ac­tiv­i­ty among 4 pa­tients, while uniQure had to set­tle for a 2% to 6.3% range for a sin­gle in­fu­sion of AMT-060. Two months lat­er Shire opt­ed to drop its ri­val gene ther­a­py in the field, the one-time leader BAX 335, in fa­vor of a pre­clin­i­cal ef­fort af­ter an­a­lysts panned the vari­able re­sults the pro­gram had post­ed.

Uniqure at­tract­ed con­sid­er­able at­ten­tion for win­ning the first Eu­ro­pean ap­proval for a gene ther­a­py. Gly­bera was green light­ed for ul­tra rare cas­es of lipopro­tein li­pase de­fi­cien­cy in 2012. But as MIT Tech­nol­o­gy Re­view’s An­to­nio Re­gal­a­do point­ed out in May, it was on­ly used once, and get­ting an ap­proval for a ques­tion­able ther­a­py that costs $1 mil­lion proved to be an Olympic chal­lenge no one else want­ed to tack­le.

The biotech dropped plans to pur­sue a US ap­proval late last year.

Soland had this to say in a state­ment:

“My de­ci­sion to re­sign as chief ex­ec­u­tive of­fi­cer is due sole­ly to per­son­al fam­i­ly rea­sons. I re­gret the abrupt na­ture of this de­ci­sion but be­lieve that it is in the best in­ter­ests of uniQure, its em­ploy­ees and share­hold­ers to en­sure that the busi­ness has the ful­ly com­mit­ted lead­er­ship it re­quires. I have con­tin­ued con­fi­dence in the Com­pa­ny’s gene ther­a­py plat­form, its re­search and clin­i­cal de­vel­op­ment pro­grams and its lead­er­ship in man­u­fac­tur­ing. I wish every­one as­so­ci­at­ed with the Com­pa­ny tremen­dous suc­cess.”

Donald and Melania Trump watch the smoke of fireworks from the South Lawn of the White House on July 4, 2020 (via Getty)

Which drug de­vel­op­ers of­fer Trump a quick, game-chang­ing ‘so­lu­tion’ as the pan­dem­ic roars back? Eli Lil­ly and Ab­Cellera look to break out of the pack

We are unleashing our nation’s scientific brilliance and will likely have a therapeutic and/or vaccine solution long before the end of the year.

— Donald Trump, July 4

Next week administration officials plan to promote a new study they say shows promising results on therapeutics, the officials said. They wouldn’t describe the study in any further detail because, they said, its disclosure would be “market-moving.”

— NBC News, July 3

Something’s cooking. And it’s not just July 4 leftovers involving stale buns and uneaten hot dogs.

Over the long weekend observers picked up signs that the focus in the Trump administration may swiftly shift from the bright spotlight on vaccines being promised this fall, around the time of the election, to include drugs that could possibly keep patients out of the hospital and take the political sting out of the soaring Covid-19 numbers causing embarrassment in states that swiftly reopened — as Trump cheered along.

So far, Gilead has been the chief beneficiary of the drive on drugs, swiftly offering enough early data to get remdesivir an emergency authorization and into the hands of the US government. But their drug, while helpful in cutting stays, is known for a limited, modest effect. And that won’t tamp down on the hurricane of criticism that’s been tearing at the White House, and buffeting the president’s most stalwart core defenders as the economy suffers.

We’ve had positive early-stage vaccine data, most recently from Pfizer and BioNTech, playing catchup on an mRNA race led by Moderna — where every little sign of potential trouble is magnified into a lethal threat, just as every advance excites a frenzy of support. But that race still has months to play out, with more Phase I data due ahead of the mid-stage numbers looming ahead. A vaccine may not be available in large enough quantities until well into 2021, which is still wildly ambitious.

So what about a drug solution?

Trump’s initial support for a panacea focused on hydroxychloroquine. But that fizzled in the face of data underscoring its ineffectiveness — killing trials that aren’t likely to be restarted because of a recent population-based study offering some support. And there are a number of existing drugs being repurposed to see how they help hospitalized patients.

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Shoshanna Shendelman, Applied Therapeutics CEO (Applied Therapeutics)

A lit­tle biotech slaps back at a 'crim­i­nal' short at­tack, vow­ing to pur­sue a pros­e­cu­tion of their case

As short attacks go, Biotech Research Partners’ assault on Applied Therapeutics’ “cherry picked” data and a variety of so-called red flags didn’t cause a whole lot of damage. Ahead of the July 4 holiday, its shares $APLT were dinged and showed signs of quick recovery.

But that didn’t stop an incendiary response, as the biotech swung into action bright and early Monday morning.

Applied Therapeutics accused the authors of the short report of manipulating graphs and figures, misrepresenting data and included factual misrepresentations — all of which added up, in their view, to fraud.

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Cel­lec­tis slammed af­ter pa­tient dies and FDA slaps a hold on their tri­al for an off-the-shelf CAR-T for mul­ti­ple myelo­ma

Cellectis was slammed after the market close on Monday as the biotech reported that the FDA demanded it hit the brakes on their MELANI-01 trial for their off-the-shelf cell therapy UCARTCS1A after one of the patients in the study died of treatment-related cardiac arrest.

The multiple myeloma patient had previously been treated unsuccessfully with various therapies, noted the biotech, and had been given dose level two (DL2) of their allogeneic CAR-T.

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UP­DAT­ED: Im­munomedics spells out PFS ben­e­fit of Trodelvy in mTNBC, hunt­ing a full OK just weeks af­ter ac­cel­er­at­ed ap­proval

By the time the FDA finally granted an accelerated OK for Immunomedics’ Trodelvy, we already got a very strong hint that their confirmatory Phase III study in metastatic triple-negative breast cancer was a success.

That’s because the independent data safety monitoring committee recommended that the trial be stopped early. But just what pointed them to the conclusion was still unclear.

“We do not know the totality of their decision other than it’s pretty evident that the primary endpoint was met; otherwise they could not request to halt the study,” Behzad Aghazadeh, the executive chairman, told Endpoints News at the time.

Bill Haney, Dragonfly CEO (Dave Pedley/Getty Images for SXSW)

A boom­ing Drag­on­fly is tak­ing its TriN­KETs to Copen­hagen as the lat­est Bris­tol My­ers pact spurs ex­pan­sion plans — out­side the US

Bristol Myers Squibb is making a habit out of collaborating with the crew at Dragonfly, adding their 3rd deal in a series that now will take them into newly charted R&D territory. And the fast-growing team at the Cambridge-based biotech is adding a facility in Copenhagen for its next growth spurt, where the government is making it easy to recruit scientists internationally as the U.S. throttles back.

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Covid-19 roundup: Teamed up with NIH, Re­gen­eron launch­es PhI­II pre­ven­tion tri­al for an­ti­body cock­tail

As Regeneron moves its antibody cocktail into Phase II/III trials testing REGN-COV2 as a treatment for both hospitalized and non-hospitalized patients with Covid-19, the biotech is also starting a Phase III in the prevention setting.

The National Institute of Allergy and Infectious Diseases — which orchestrated the large, randomized study for remdesivir that produced positive results — will jointly run the study.

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Douglas Love, Annexon CEO (Annexon)

IPO bound? Ac­tu­al­ly, An­nex­on was al­ready prepped and primed to toss its S-1 to Wall Street as in­vestors ral­lied

The Wall Street IPO shuffle generally calls for a little distance between the crossover ante and the Wall Street double, but with the window on the street wide open and biotech sizzling hot, who’s waiting?

The crew at Annexon didn’t leave anyone in suspense for long about their IPO plans. A day after the Bay Area biotech with clinical plans to target neurodegeneration quietly unveiled a $100 million raise, they were back with an S-1 outlining a pitch to double that — or more.

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Jean-Paul Clozel, Idorsia CEO (Patrick Straub/Keystone via AP Images)

Sec­ond PhI­II study for Idor­si­a's sleep drug re­turns pos­i­tive re­sults, but al­so rais­es new ques­tions

Following a successful Phase III study in April showcasing the safety and potential of its new sleep drug, Idorsia posted some mixed news in the second Phase III study, but that won’t stop a planned filing aimed at regulatory approval.

The drug, a dual orexin receptor antagonist (DORA) called daridorexant, was found to significantly improve sleep maintenance and subjective total sleep time in 25 mg doses, replicating results from the first Phase III study. However, improvements in sleep onset and daytime functioning narrowly missed statistical significance, despite numerical consistency with the April study.

George Yancopoulos (Regeneron)

UP­DAT­ED: Re­gen­eron co-founder George Yan­copou­los of­fers a com­bat­ive de­fense of the po­lice at a high school com­mence­ment. It didn’t go well

Typically, the commencement speech at Yorktown Central School District in Westchester — like most high schools — is an opportunity to encourage students to face the future with confidence and hope. Regeneron president and co-founder George Yancopoulos, though, went a different route.

In a fiery speech, the outspoken billionaire defended the police against the “prejudice and bias against law enforcement” that has erupted around the country in street protests from coast to coast. And for many who attended the commencement, Yancopoulos struck the wrong note at the wrong time, especially when he combatively challenged someone for interrupting his speech with a honk for “another act of cowardness.”

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