Re­searchers out­line an­oth­er big dis­ease tar­get for No­var­tis’ canakinum­ab as drug slash­es rate of gout flares

We’ve al­ready seen No­var­tis’ out­line of pos­i­tive da­ta un­der­scor­ing canakinum­ab’s abil­i­ty to re­duce risks for car­dio pa­tients by tamp­ing down on the in­ter­leukin-1β path­way. Now re­searchers have al­so out­lined how it may help peo­ple suf­fer­ing from gout.

Vas Narasimhan

The da­ta are com­ing from a sec­ondary analy­sis of the big CAN­TOS study, which No­var­tis is us­ing to make its bid for a po­ten­tial block­buster car­dio OK. In­ves­ti­ga­tors divvied up pa­tients by low, medi­um and high scores based on their serum urate lev­el, which trig­gers painful gout flares. And they found the drug slashed the rate of gout flares by more than half in all three com­pared to place­bo, with a haz­ard ra­tio start­ing at 0.40, then 0.48 and 0.45 for the high group.

The drug, though, did re­duce high sen­si­tiv­i­ty C-re­ac­tive pro­tein (hsCRP), as has al­ready been not­ed in the car­dio work.

Daniel Solomon

Back in No­vem­ber, No­var­tis’ $NVS then de­vel­op­ment chief and now CEO Vas Narasimhan said that the drug proved more clear­ly im­pact­ful for heart at­tack pa­tients whose hsCRP lev­el — a mea­sure of in­flam­ma­tion us­ing high-sen­si­tiv­i­ty C-re­ac­tive pro­tein — fell be­low 2mg/L af­ter three months of treat­ment. By that score, they tracked a 31% re­duc­tion in car­dio­vas­cu­lar death and a 31% re­duc­tion in all-cause mor­tal­i­ty.

Canakinum­ab is cur­rent­ly ap­proved for rare in­flam­ma­to­ry con­di­tions, but No­var­tis has a much, much big­ger mar­ket in mind.

No­var­tis suc­cess in car­dio took a num­ber of an­a­lysts by sur­prise, and the phar­ma gi­ant has big plans for break­ing in­to a tough mar­ket. Iron­wood, mean­while, has been mar­ket­ing lesin­u­rad for gout af­ter li­cens­ing it from As­traZeneca, which gath­ered mixed da­ta on its im­pact.

“Our re­sults demon­strate a strik­ing ef­fect of canakinum­ab on re­duc­ing the risk of gout at­tacks in ath­er­o­scle­ro­sis pa­tients,” said Daniel Solomon, Pro­fes­sor of Med­i­cine, Har­vard Med­ical School and Brigham and Women’s Hos­pi­tal. “More­over, these da­ta il­lus­trate serum urate as a risk mark­er for both gout and car­dio­vas­cu­lar events, though canakinum­ab has no ef­fect on serum urate lev­els due to its mech­a­nism of ac­tion.”

UP­DAT­ED: In a stun­ning turn­around, Bio­gen says that ad­u­canum­ab does work for Alzheimer's — but da­ta min­ing in­cites con­tro­ver­sy and ques­tions

Biogen has confounded the biotech world one more time.

In a stunning about-face, the company and its partners at Eisai say that a new analysis of a larger dataset on aducanumab has restored its faith in the drug as a game-changer for Alzheimer’s and, after talking it over with the FDA, they’ll now be filing for an approval of a drug that had been given up for dead.

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Vas Narasimhan. Getty Images

UP­DAT­ED: Failed PhI­II fe­vip­iprant tri­als pour more cold wa­ter on No­var­tis' block­buster R&D en­gine — and briefly spread the chill to a high-pro­file biotech

Back in July, during an investor call where Novartis execs ran through an upbeat assessment of their Q2 performance, CEO Vas Narasimhan and development chief John Tsai were pressed to predict which of the two looming Phase III readouts — involving cardio drug Entresto and asthma therapy fevipiprant, respectively — had a higher likelihood of success. Tsai gave the PARAGON-HF study with Entresto minimally better odds, but Narasimhan emphasized that their strategy of giving fevipiprant to more severe patients gave them confidence.

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UP­DAT­ED: The FDA sets a reg­u­la­to­ry speed record, pro­vid­ing a snap OK for Ver­tex's break­through triplet for cys­tic fi­bro­sis

The FDA has approved Vertex’s new triplet for cystic fibrosis at a record-setting speed.

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David Liu, Liu Group

David Liu un­veils newest ad­vance­ment in CRISPR tech: Prime edit­ing

The researcher behind base-editing is out with what some scientists are hailing as the biggest advancement in CRISPR technology since that 2016 breakthrough: “prime editing.” The new molecular gadget is capable of erasing any base pair and stenciling in another and cutting or adding long segments of DNA without breaking both strands of the helix.

David Liu, base editing pioneer and founder of Beam Therapeutics, published the findings in Nature alongside Andrew Anzalone. They estimated that the breakthrough “in principle” puts 89% of human diseases in purview — although experts cautioned that human therapies were a long way off.

Bhaskar Chaudhuri. Frazier Healthcare Partners

Fra­zier Health­care Part­ner­s' der­ma­tol­ogy up­start at­tracts a mar­quee syn­di­cate, $94M+ for 'in-be­tween' top­i­cal drug

For the past three years Frazier Healthcare Partners’ Bhaskar Chaudhuri has been carefully and quietly grooming Arcutis Therapeutics, a new dermatology play he co-founded to deliver topical formulations of well-known drugs. Now that the biotech is poised to enter Phase III, he’s being joined by a marquee syndicate for its $94.5 million Series C.

HBM Healthcare Investments, Vivo Capital, BlackRock, Omega Funds, Pivotal BioVentures, and Goldman Sachs jumped on board, joining Bain Capital Life Sciences, OrbiMed and RA Capital Management in backing Arcutis’ lead topical cream for plaque psoriasis.

A new com­pa­ny en­ters the Tec­fidera fight, of­fer­ing to kill two birds

The remedy for the most common side effect for one of the most common multiple sclerosis drugs is simple: aspirin.

Taking aspirin with Biogen’s Tecfidera will reduce the flush, a sometimes painful form of red skin irritation, many patients experiences. The problem is that the aspirin has to be taken at least 30 minutes before Tecfidera, turning a simple twice-a-day, one-dose oral drug into a staggered two-drug regimen.

UP­DAT­ED: Bris­tol-My­ers makes Op­di­vo pitch for front­line lung can­cer with open la­bel PhI­II study

Despite a head start, when Bristol-Myers Squibb and its pioneering checkpoint inhibitor Opdivo suffered a key lung cancer setback in 2016, they found themselves relegated to the backseat as Merck’s Keytruda seized the wheel on the road to immunotherapy stardom. Bristol-Myers has since suffered blow after blow in its quest to take a big slice of the lucrative market, peppered with some small successes. On Tuesday, the New Jersey drugmaker touted positive data from a Phase III open-label study in a bid to carve itself a piece of the frontline lung cancer market.

Take­da tees up $420M deal for celi­ac an­ti­dote, con­tin­u­ing R&D re­fo­cus

Sometime in the 1st century AD, a patient presented to Arataeus looking like a varicose ghost. He was “emaciated and atrophied, pale, feeble and incapable of performing any of his accustomed works,” the Greek physician wrote, with hollow temples and huge veins running all over his body.

A dysfunctional digestive system, Arataeus concluded – an imbalance he attributed to a “heat” deficiency in a system he and other Greeks regarded as functioning similarly to an oven – and coined a term: coeliac disease, after the Greek word for abdomen.

IM­brave150: Roche’s reg­u­la­to­ry crew plans a glob­al roll­out of Tecen­triq com­bo for liv­er can­cer as PhI­II scores a hit

Just weeks after Bristol-Myers Squibb defended its failed pivotal study pitting Opdivo against Nexavar in liver cancer, Roche says it’s beat the frontline challenge with a combination of their PD-L1 Tecentriq with Avastin. And now they’re rolling their regulatory teams in the US, Europe and China in search of a new approval — badly needed to boost a trailing franchise effort.
Given their breakthrough and Big Pharma status as well as the use of two approved drugs, FDA approval may well prove to be something of a formality. And the Chinese have been clear that they want new drugs for liver cancer, where lethal disease rates are particularly high.
Researchers at their big biotech sub, Genentech, say that the combo beat Bayer’s Nexavar on both progression-free survival as well as overall survival — the first advance in this field in more than a decade. We won’t get the breakdown in months of life gained, but it’s a big win for Roche, which has lagged far, far behind Keytruda and Opdivo, the dominant PD-1s that have captured the bulk of the checkpoint market so far.
Researchers recruited hepatocellular carcinoma — the most common form of liver cancer — patients for the IMbrave150 study who weren’t eligible for surgery ahead of any systemic treatment of the disease.
Roche has a fairly low bar to beat, with modest survival benefit for Nexavar, approved for this indication 12 years ago. But they also plan to offer a combo therapy that could have significantly less toxicity, offering patients a much easier treatment regimen.
Cowen’s Steven Scala recently sized up the importance of IMbrave150, noting:

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