No­var­tis’ re­cent­ly de­part­ed on­col­o­gy R&D chief is head­ed back to Dana-Far­ber and a new job in can­cer re­search

Bill Sell­ers

The re­volv­ing door at No­var­tis has spit out an­oth­er top ex­ec­u­tive, on­ly this one is head­ed back to a fac­ul­ty post at Dana-Far­ber Can­cer In­sti­tute and Har­vard Med­ical School.

William Sell­ers had been in charge of on­col­o­gy re­search at No­var­tis be­fore he an­nounced his “re­tire­ment” ear­li­er this year. But his 11-year stint at the No­var­tis In­sti­tutes for Bio­Med­ical Re­search was not his fi­nal turn at bat in drug re­search. His new fac­ul­ty post in­cludes re­spon­si­bil­i­ties as a se­nior ad­vis­er on ex­per­i­men­tal meds. And he’ll still be di­rect­ly en­gaged on ear­ly-stage drug de­vel­op­ment at Dana-Far­ber, where he’ll help guide a spec­trum of work that runs from tar­get val­i­da­tion to ear­ly hu­man stud­ies.

His re­turn to aca­d­e­m­ic R&D cir­cles — which in­cludes a po­si­tion with The Broad In­sti­tute — comes at a time of tur­moil for No­var­tis, which has seen a large num­ber of se­nior ex­ecs leave this year. And that’s been not­ed with con­cern by some of the an­a­lysts fol­low­ing the phar­ma gi­ant.

“Over the years, the com­pa­ny has been like a re­volv­ing door when it comes to se­nior man­agers de­part­ing — be­low the CEO lev­el, that is,” wrote Tim An­der­son, a Bern­stein an­a­lyst quot­ed by Reuters. “We have won­dered if this has con­tributed to pe­ri­od­ic short­falls at the com­pa­ny, be­cause of a lack of con­ti­nu­ity.”

While the Cam­bridge/Boston hub is get­ting back a top aca­d­e­m­ic re­searcher, it’s al­so been a source of tal­ent for Big Phar­ma in gen­er­al, and No­var­tis in par­tic­u­lar. Jay Brad­ner left his post as a physi­cian-sci­en­tist at Dana-Far­ber to take the reins at NI­BR last fall.

Sell­ers built a rep­u­ta­tion for his ear­ly work in can­cer genome se­quenc­ing at Dana-Far­ber, which helped him in his work study­ing mol­e­c­u­lar path­ways of can­cer at No­var­tis. And he plans to stay fo­cused on on­col­o­gy in his new fac­ul­ty po­si­tion.

“Bill Sell­ers is one of the ear­ly pi­o­neers in the ap­pli­ca­tion of sys­tem­at­ic genome analy­sis to can­cer and was in­volved in the ear­ly days of the Broad,” said Broad In­sti­tute found­ing di­rec­tor Er­ic Lan­der. “As a fac­ul­ty mem­ber, his re­search will con­tin­ue to help ad­vance our un­der­stand­ing of the mech­a­nisms of can­cer and how best to tar­get them for bet­ter di­ag­nos­tics and treat­ment.

'Chang­ing the whole game of drug dis­cov­ery': Leg­endary R&D vet Roger Perl­mut­ter leaps back in­to work as a biotech CEO

Roger Perlmutter needs no introduction to anyone remotely involved in biopharma. As the R&D chief first at Amgen and then Merck, he’s built a stellar reputation and a prolific career steering new drugs toward the market for everything from cancer to infectious diseases.

But for years, he’s also held a less known title: science partner at The Column Group, where he’s regularly consulted about the various ideas the VCs had for new startups.

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The DCT-OS: A Tech­nol­o­gy-first Op­er­at­ing Sys­tem - En­abling Clin­i­cal Tri­als

As technology-enabled clinical research becomes the new normal, an integrated decentralized clinical trial operating system can ensure quality, deliver consistency and improve the patient experience.

The increasing availability of COVID-19 vaccines has many of us looking forward to a time when everyday things return to a state of normal. Schools and teachers are returning to classrooms, offices and small businesses are reopening, and there’s a palpable sense of optimism that the often-awkward adjustments we’ve all made personally and professionally in the last year are behind us, never to return. In the world of clinical research, however, some pandemic-necessitated adjustments are proving to be more than emergency stopgap measures to ensure trial continuity — and numerous decentralized clinical trial (DCT) tools and methodologies employed within the last year are likely here to stay as part of biopharma’s new normal.

UP­DAT­ED: Pfiz­er hits the brakes on their piv­otal tri­al for a BC­MA/CD3 bis­pe­cif­ic on safe­ty con­cerns while FDA road­block is hold­ing up Duchenne MD PhI­II

Pfizer’s ambitious plan to take a Phase II study of its BCMA CD3-targeted bispecific antibody elranatamab (PF-06863135) and run it through to an accelerated approval has derailed.

The pharma giant said in a release this morning that they have halted enrollment for their MagnetisMM-3 study after researchers tracked three cases of peripheral neuropathy in the ongoing Phase I. They are now sharing info with the FDA as they explore the red safety flag.

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Cynthia Butitta (L) and Joe Jimenez

Is that an­oth­er IPO in the mak­ing? Ex-No­var­tis CEO Joe Jimenez and a lead Kite play­er take up new posts at an off-the-shelf ri­val to 2 pi­o­neer­ing drugs

Right on the heels of taking on a $160 million crossover round in a likely leap to Nasdaq, Century Therapeutics CEO Lalo Flores is now pushing ahead with the high-profile ex-Novartis chief Joe Jimenez as chairman.

Jimenez’s greatest fame at Novartis was earned for one of its weakest products, as their pioneering personalized CAR-T Kymriah won the honors for the first such drug to make it to the market. Now a host of players, including Century, are barreling in behind the frontrunners with allogeneic rivals that can be created for off-the-shelf use.

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FDA ex­tends re­search agree­ment with MIT-li­censed or­gan-on-chip sys­tems

The FDA on Wednesday extended its four-year agreement with CN Bio, a developer of single- and multi-organ-on-chip systems used for drug discovery, for another three years.

CN Bio said the scope of the research performed by the FDA’s Center for Drug Evaluation and Research has expanded to include the exploration of the company’s lung-on-a-chip system to help with the agency’s evaluation of inhaled drugs, in addition to the agency’s work on its liver model.

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In quest to meet user fee goals, FDA’s per­for­mance con­tin­ues down­ward trend

A recent update to the FDA’s running tally of how it’s meeting its user fee-related performance goals during the pandemic shows an agency that is not out of the woods yet.

The latest numbers reveal that for a second straight quarter in 2021, the FDA has met its user fee goal dates for 93% of original new drug applications, which compares with 94% and 98% for the previous two quarters in 2020, respectively.

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Joe Wiley, Amryt CEO

A biotech with a yen for pricey rare dis­ease drugs — and bar­gain base­ment shop­ping — adopts an­oth­er or­phan in lat­est M&A pact

After making it through a long, painful haul to get past a CRL and on to an FDA approval last summer, little Chiasma has found a buyer.

Amryt $AMYT, a company known for its appetite for acquiring expensive drugs for rare diseases at bargain prices, snagged Chiasma and its acromegaly drug Mycapssa (octreotide) capsules in an all-stock deal — with an exchange of 0.396 shares of Amryt for every share of Chiasma.

Ngozi Okonjo-Iweala, Director general of WTO (AP Photo/Keystone/Alessandro Della Bella)

Opin­ion: Waiv­ing Covid-19 vac­cine IP could save lives, but where is the man­u­fac­tur­ing ca­pac­i­ty?

Droves of House Democrats in Washington and members of the European Parliament have now glommed onto a major push by India and South Africa at the WTO to abolish all IP around Covid-19 vaccines.

At first blush, waiving this IP sounds like an easy win: More Covid-19 vaccines made locally for more people means more lives saved. Simple enough, especially as low-income countries have received just a tiny fraction of the world’s vaccine allotment so far.

Thomas Schall, ChemoCentryx CEO (file photo)

Chemo­Cen­tryx plunges as FDA rais­es ques­tions about rare dis­ease drug ahead of ad­comm

ChemoCentryx’s stock price on Wednesday was cut in half by the release of FDA briefing documents ahead of a Thursday adcomm, raising questions on the company’s clinical data to support avacopan as a treatment for adults with a rare and serious disease known as anti-neutrophil cytoplasmic autoantibody (ANCA)-vasculitis.

ANCA-associated vasculitides (AAV) affect small to medium-size blood vessels that can be fatal in less than a year if left untreated, according to FDA. Only Roche’s Rituxan is currently FDA-approved for the treatment of AAV, while glucocorticoids are approved for the broader indication of vasculitis.

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