Sanofi re­cruits No­var­tis' top phar­ma ex­ec Paul Hud­son as its new CEO — so what hap­pens now?

Sanofi’s board has turned to some­one who’s not French to be its next CEO.

The Paris-based phar­ma gi­ant named No­var­tis phar­ma chief Paul Hud­son — a British phar­ma ex­ec­u­tive with an in­ter­na­tion­al pedi­gree — to the top post as cur­rent CEO Olivi­er Brandi­court heads off to an ear­ly “re­tire­ment.”

Marie-France Tschudin AAA

In a care­ful­ly or­ches­trat­ed re­sponse, No­var­tis CEO Vas Narasimhan con­grat­u­lat­ed Hud­son and named Marie-France Tschudin, a Swiss cit­i­zen who’s head­ing up the re­cent­ly ac­quired can­cer group Ad­vanced Ac­cel­er­a­tor Ap­pli­ca­tions, as Hud­son’s re­place­ment. In do­ing so, he im­me­di­ate­ly po­si­tioned Tschudin — who speaks 6 lan­guages — as a top can­di­date for any fu­ture Big Phar­ma CEO open­ing.

Hud­son joined No­var­tis and the ex­ec­u­tive com­mit­tee just three years ago, af­ter serv­ing as the US phar­ma chief for As­traZeneca. He has a de­gree in eco­nom­ics from Man­ches­ter Met­ro­pol­i­tan Uni­ver­si­ty in the UK.

Hud­son will take the top slot on Sep­tem­ber 1, where he’ll be greet­ed by an ex­tra­or­di­nary chal­lenge. The com­pa­ny has an R&D group with a rep for slow mo­tion move­ment and a mar­ket­ing team that’s faced with some tough chal­lenges on the di­a­betes front, among oth­ers.

In­vestors re­spond­ed warm­ly to the ac­tion, bid­ding Sanofi’s shares up 5.5%  on Fri­day.

Brandi­court came on board just 4 years ago, fol­low­ing in the wake of Chris Viehbach­er, who was axed by the Gal­lic board and pow­er­ful chair­man — Serge Wein­berg — in charge of Sanofi af­ter mov­ing back home to the US. The French clear­ly want­ed a na­tive to run the com­pa­ny at the time, but ap­par­ent­ly feel that pro­fes­sion­al­ism trumps na­tion­al­i­ty as it works to­ward a turn­around.

One of Reuters sources, who tipped the wire ser­vices off ear­ly on the an­nounce­ment, said that Hud­son was picked be­cause of his sol­id man­age­ment ex­pe­ri­ence and ex­pe­ri­ence with dig­i­tal tech­nolo­gies, where No­var­tis has been care­ful­ly fo­cused.

So now the guess­ing games be­gin. What will Hud­son do to shake things up at Sanofi, where its R&D or­ga­ni­za­tion has pro­duced lit­tle of re­al val­ue, with the pos­si­ble ex­cep­tion of their late-stage can­cer drug isat­ux­imab?

Sanofi ex­e­cut­ed ma­jor al­liances with Re­gen­eron and Al­ny­lam on ground­break­ing drugs, but on its own the com­pa­ny is known as large­ly mori­bund and bu­reau­crat­ic, tak­ing a long stretch to fi­nal­ly ex­e­cute on the M&A front un­der Brandi­court. And now they’ve backed away from those al­liances to lean more heav­i­ly on the pipeline and R&D chief John Reed.

If Hud­son’s back­ground at No­var­tis is an in­di­ca­tor, he may turn to deal­mak­ing to help en­liv­en the late-stage pipeline, where all big phar­mas are judged. An in­ter­nal shake­up in key ar­eas like on­col­o­gy may al­so be in the off­ing, as new ex­ecs like Di­et­mar Berg­er join up. And just about every new CEO — Dave Ricks and Em­ma Walm­s­ley, for ex­am­ple — like to bring out the axe to chop away at the dead wood be­fore adding any­thing.

Reed has al­ready re­vamped the pipeline. But look for an even greater re­liance on the US re­search ops around Boston to car­ry the bulk of the weight.

Any­one look­ing for the next sig­nal on Hud­son’s sta­tus should look to his com­pen­sa­tion pack­age. Brandi­court took home a 2018 com­pen­sa­tion pack­age of $8.1 mil­lion — down $2.7 mil­lion, a painful 33% drop — com­pared to his al­lot­ment for 2017. Eu­ro­pean ex­ecs tend to be paid sig­nif­i­cant­ly less than their US coun­ter­parts, but a cut in com­pen­sa­tion like that un­der­scored the board’s feel­ings about Brandi­court’s lack of ef­fec­tive­ness as a man­ag­er.

How much did Hud­son get in his ne­go­ti­a­tions?

Im­age: Paul Hud­son (No­var­tis)

 

Mi­no­ryx and Sper­o­genix ink an ex­clu­sive li­cense agree­ment to de­vel­op and com­mer­cial­ize lerigli­ta­zone in Chi­na

September 23, 2020 – Hong Kong, Beijing, Shanghai (China) and Mataró, Barcelona (Spain)  

Minoryx will receive an upfront and milestone payments of up to $78 million, as well as double digit royalties on annual net sales 

Sperogenix will receive exclusive rights to develop and commercialize leriglitazone for the treatment of X-linked adrenoleukodystrophy (X-ALD), a rare life-threatening neurological condition

FDA chief Stephen Hahn on Capitol Hill earlier this week (Getty Images)

As FDA’s work­load buck­les un­der the strain, Trump again ac­cus­es the agency of a po­lit­i­cal hit job

Peter Marks appeared before a virtual SVB Leerink audience yesterday and said that his staff at FDA’s CBER is on the verge of working around the clock. Manufacturing inspections, policy work and sponsor communications have all been pushed down the to-do list so that they can be responsive to Covid-related interactions. And the agency’s objective right now? “To save as many lives as we can,” Marks said, likening the mortality on the current outbreak as equivalent to “a nuclear bomb on a small city.”

The win­dow is wide open as four more biotechs join the go-go IPO class of 2020

It’s another day of hauling cash in the biopharma world as four more IPOs priced Friday and a fifth filed its initial paperwork.

The biggest offering comes from PMV Pharma, an oncology biotech focusing on p53 mutations, which raised $211.8 million after pricing shares at $18 apiece. Prelude Therapeutics, developing PRMT5 inhibitors for rare cancers, was next with a $158 million raise, pricing shares at $19 each. Graybug Vision raised $90 million after pricing at $16 per share for its wet AMD candidates, and breast cancer biotech Greenwich Lifesciences brought up the rear with a small, $7 million raise after pricing shares at $5.75.

J&J of­fers PhI/IIa da­ta show­ing its sin­gle-dose vac­cine can stir up suf­fi­cient im­mune re­sponse

Days after J&J dosed the first participants of its Phase III ENSEMBLE trial, the pharma giant has detailed the early-stage data that gave them confidence in a single-dose regimen.

Testing two dose levels either as a single dose or in a two-dose schedule spaced by 56 days in, the scientists from Janssen, the J&J subsidiary developing its vaccine, reported that the low dose induced a similar immune response as the high dose. The interim Phase I/IIa results were posted in a preprint on medRxiv.

Daniel O'Day, Gilead CEO (Kevin Dietsch/UPI/Bloomberg via Getty Images)

Play-by-play of Gilead­'s $21B Im­munomedics buy­out de­tails a fren­zied push — and mints a new biotech bil­lion­aire

Immunomedics had not really been looking for a buyout when the year began. Excited by its BLA for Trodelvy, submitted to the FDA in late 2019, executive chairman Behzad Aghazadeh started off looking for potential licensing deals and zeroed in on four potential partners, including Gilead, following January’s JP Morgan Healthcare Conference in San Francisco. Such talks advanced throughout the year, with discussions advancing to the second round in mid-August.

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President Donald Trump reacts after signing an executive order following his remarks on his healthcare policies yesterday in Charlotte, North Carolina (Getty Images)

Op-ed: Will phar­ma re­al­ly pay for Trump’s lat­est law­less promise to 33 mil­lion Medicare ben­e­fi­cia­ries? Not like­ly

Sitting atop the executive branch, President Donald Trump is the ultimate authority at the FDA. He can fast track any vaccine to approval himself. If it came to that, of course.

What he can’t do is unilaterally order the legislative branch to loosen the Treasury’s coffers for $6.6 billion. Nor can he command pharmaceutical companies to pay for $200 vouchers sent to 33 million Medicare beneficiaries for prescription drugs before the election.

New York governor Andrew Cuomo (AP Images)

An­drew Cuo­mo says New York will un­der­take its own vac­cine re­view process, and wouldn’t rec­om­mend trust­ing the fed­er­al gov­ern­ment

The concerns keep mounting over President Donald Trump’s politicization of the FDA and other federal agencies guiding the development of a safe and effective vaccine. And today, the telegenic New York governor Andrew Cuomo appeared to introduce even more politics into the matter — latest in an ongoing series of incidents that have cast the proudly independent FDA in starkly political terms.

During his daily press conference Cuomo said that the state will review any coronavirus vaccines approved by the federal government, citing a lack of trust in the Trump administration. The announcement comes one day after Trump accused the FDA of making an “extremely political” move in proposing stricter vaccine guidance.

President Trump walks past HHS secretary Alex Azar (Getty Images)

Azar falls in line un­der Trump again. Ex­perts say he's re­in­forc­ing a dark sig­nal sent to the FDA

In the latest incident where Alex Azar has steadfastly taken the side of President Donald Trump over that of the FDA, the HHS secretary was noncommittal this morning when asked if he supports the attempt by his subordinates at the FDA to strengthen guidelines for a vaccine EUA.

Appearing on NBC’s Today Show, the HHS secretary muddied the waters, stating that the guidance that matters is the one that is “actually already out there.”

Covid-19 roundup: Op­er­a­tion Warp Speed's 7th vac­cine is live at­ten­u­at­ed; Small biotech touts big suc­cess where gi­ants have failed

Operation Warp Speed is stacking its vaccine portfolio with a “TBD” new candidate: a live attenuated vaccine that can be administered in a single dose, potentially as an oral formulation rather than an injection.

Sound familiar?

That could be because the unannounced candidate appears to match the profile of an inoculation being developed by Merck, according to Bloomberg, which first reported the development based on a presentation by Moncef Slaoui.

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