Jean-François Pariseau and Dion Madsen, Amplitude

New Am­pli­tude fund looks to bet over $100 mil­lion on in­cip­i­ent Cana­di­an biotech mar­ket

Two top Cana­di­an ven­ture cap­i­tal­ists and the Busi­ness De­vel­op­ment Bank of Cana­da have raised over $70 mil­lion for a new fund aimed sharply at fund­ing promis­ing ideas emerg­ing from the “un­der-fund­ed” Cana­di­an bio­phar­ma and health­care sec­tor.

Jean-François Pariseau and Dion Mad­sen have spun out their health­care di­vi­sion of BDC Cap­i­tal in­to the Am­pli­tude fund. They’ve raised over CAD $100 mil­lion ($76 mil­lion USD) with a goal of CAD $200 mil­lion ($152 mil­lion USD), to bol­ster pre­ci­sion med­i­cine north of the 49th par­al­lel. 

Cana­da may seem like an un­like­ly place to chan­nel VC health­care dol­lars, but Mad­sen said that’s part of the point. The fund will fo­cus on three pri­or­i­ties — tar­get­ed ther­a­pies such as cell and im­munother­a­py, med­ical imag­ing and ar­ti­fi­cial in­tel­li­gence — they see as promis­ing but un­der­fund­ed com­pared with ma­jor mar­kets like the US and Eu­rope. 

“We see world-class in­no­va­tion here, this is com­pet­i­tive as any­thing we see emerg­ing from any aca­d­e­m­ic cen­ters around the world, but it’s rel­a­tive­ly un­in­vest­ed,” Mad­sen told End­points News. “So we see a tremen­dous op­por­tu­ni­ty.”

Mad­sen said he and Pariseau had the idea for the new fund two years ago. The aim was to build a deep­er staff and a larg­er re­source pool to back — “am­pli­fy” — a strat­e­gy they had de­vel­oped over years at BDC Cap­i­tal, where they over­saw a CAD $270 mil­lion port­fo­lio.

There, the two had sur­veyed bio­phar­ma strate­gies in the US, Eu­rope, and across Asia. See­ing Cana­di­an com­pa­nies ac­quired ear­ly or sput­ter for a lack of funds, Mad­sen said, they de­cid­ed to pro­vide cap­i­tal, tech or that could lead them to­ward an IPO. They in­vest­ed in 11 com­pa­nies. The re­sults in­clud­ed rare dis­ease and on­col­o­gy biotechs Clemen­tia and Zymeworks, along with car­dio­vas­cu­lar-fo­cused Mile­stone Phar­ma­ceu­ti­cals.

“Cana­da had sci­en­tif­ic plat­forms and in­no­va­tion that was re­al­ly not cap­tured be­cause it was be­ing un­der­fund­ed and sold off,” Mad­sen said.

The fund of­fi­cial­ly spun out in Ju­ly 2018 and had their first close to­day. They made their first in­vest­ment this sum­mer as part of pre­ci­sion on­col­o­gy start­up Re­pare Ther­a­peu­tics’ $82.5 mil­lion Se­ries B, which closed in Sep­tem­ber.

Lloyd Se­gal

Re­pare us­es CRISPR gene-edit­ing tech­nol­o­gy to iden­ti­fy new small mol­e­cule tar­gets for can­cer. It has at­tract­ed in­vest­ment in­ter­est most no­tably from Ver­sant, but CEO Lloyd Se­gal said he and oth­er Cana­di­an ex­ec­u­tives have known Mad­sen and Pariseau for years and that gives them an ad­van­tage.

“Cana­da is not nec­es­sar­i­ly on the beat­en path of where the tier 1 VCs glob­al­ly go look for com­pa­nies, and they do a great job of putting those com­pa­nies on­to the radar screen,” Se­gal told End­points. “They make it their busi­ness to un­der­stand the play­ers in Cana­da far more deeply be­cause that’s their day job. That’s their edge.”

Michel Vounatsos, Biogen CEO (via YouTube)

UP­DAT­ED: Bio­gen spot­lights a pair of painful pipeline set­backs as ad­u­canum­ab show­down looms at the FDA

Biogen has flagged a pair of setbacks in the pipeline, spotlighting the final failure for a one-time top MS prospect while scrapping a gene therapy for SMA after the IND was put on hold due to toxicity.

Both failures will raise the stakes even higher on aducanumab, the Alzheimer’s drug that Biogen is betting the ranch on, determined to pursue an FDA OK despite significant skepticism they can make it with mixed results and a reliance on post hoc data mining. And the failures are being reported as Biogen was forced to cut its profit forecast for 2020 as a generic rival started to erode their big franchise drug.

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A new chap­ter in the de­cen­tral­ized clin­i­cal tri­al ap­proach

Despite the promised decentralized trial revolution, we haven’t yet moved the needle in a significant way, although we are seeing far bolder commitments to this as we continue to experience the pandemic restrictions for some time to come. The vision of grandeur is one thing, but operationalizing and execution are another and recognising that change, particularly mid-flight on studies, is worthy of thorough evaluation and consideration in order to achieve success. Here we will discuss one of the critical building blocks of a Decentralized and Remote Trial strategy: TeleConsent; more than paper under glass, it is a paradigm change and key digital enabler.

Stephen Hahn, FDA commissioner (AP Images)

As FDA sets the stage for the first Covid-19 vac­cine EUAs, some big play­ers are ask­ing for a tweak of the guide­lines

Setting the stage for an extraordinary one-day meeting of the Vaccines and Related Biological Products Advisory Committee this Thursday, the FDA has cleared 2 experts of financial conflicts to help beef up the committee. And regulators went on to specify the safety, efficacy and CMC input they’re looking for on EUAs, before they move on to the full BLA approval process.

All of this has already been spelled out to the developers. But the devil is in the details, and it’s clear from the first round of posted responses that some of the top players — including J&J and Pfizer — would like some adjustments and added feedback. And on Thursday, the experts can offer their own thoughts on shaping the first OKs.

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David Hung (file photo)

Mas­ter deal­mak­er David Hung re­tools a SPAC sedan in­to a fi­nanc­ing mus­cle ve­hi­cle that leaves his can­cer start­up with $850M and a place on Wall Street

It’s only right that one of the industry’s top dealmakers just completed one of the biggest SPAC-related deals in the pipeline.

David Hung, of Medivation fame, has completed a back flip into the market, merging with EcoR1 Capital’s SPAC Panacea and landing neatly on Wall Street with an $NUVB stock ticker after filling out the blank check in his name. In addition to the $144 million held in the SPAC — provided none of the investors opt out — Hung is getting ahold of $500 million more being chipped in by a slate of institutional investors who feel that Hung could have the keys to another Medivation-style success.

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Pfizer CEO Albert Bourla (Drew Angerer/Getty Images)

Pfiz­er is on the verge of claim­ing a multi­bil­lion-dol­lar first-mover ad­van­tage with their Covid-19 vac­cine — an­a­lyst

From the beginning, Pfizer CEO Albert Bourla eschewed government funding for his Covid-19 vaccine work with BioNTech, willing to take all the $2 billion-plus risk of a lightning-fast development campaign in exchange for all the rewards that could fall its way with success. And now that the pharma giant has seized a solid lead in the race to the market, those rewards loom large.

SVB Leerink’s Geoff Porges has been running the numbers on Pfizer’s vaccine, the mRNA BNT162b2 program that the German biotech partnered on. And he sees a $3.5 billion peak in windfall revenue next year alone. Even after the pandemic is brought to heel, though, Porges sees a continuing blockbuster role for this vaccine as people around the world look to guard against a new, thoroughly endemic virus that will pose a permanent threat.

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CEO Grace Colón (InCarda)

Look­ing to re­pur­pose an old drug to treat ir­reg­u­lar heart­beats, In­Car­da rais­es $30M in first Se­ries C close

A little less than two years after completing its $42 million Series B round, InCarda has returned to the venture well.

The San Francisco-based biotech announced the first portion of its Series C on Wednesday, pulling in $30 million in new funding. Most of the money will give enough runway for InCarda’s InRhythm program, an inhaled therapeutic aiming to treat sudden episodes of irregular heartbeats, through its Phase II trials and prepare it for Phase III.

UP­DAT­ED: CRISPR Ther­a­peu­tics gets a snap­shot of off-the-shelf CAR-T suc­cess in B-cell ma­lig­nan­cies — marred by the death of a pa­tient

Just days after scientific founder Emmanuelle Charpentier shared the Nobel prize for her work on CRISPR/Cas9, CRISPR Therapeutics $CRSP is showing off a snapshot of success in their early-stage study for an off-the-shelf CAR-T approach to CD19+ B cell malignancies — a snapshot marred by the death of a patient who had been given a high dose of the treatment.

Using their gene editing tech, researchers for CRISPR engineered cells from healthy donors into an attack vehicle aimed at cancer, something that has been achieved with great success using patients’ own cells — the autologous approach. But autologous CAR-T is hampered by the more complex vein-to-vein requirement that delays treatment, and now CRISPR Therapeutics along with other players like Allogene are determined to replace the pioneers with CAR-T 2.0.

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Steve Chen, Cellis Therapeutics president and CMO (Cellics)

UC San Diego spin­out award­ed up to $15M for nanosponge de­signed to soak up sep­sis-caus­ing tox­ins

CARB-X, a global partnership looking to spur the development of new antibacterial drugs, is awarding Cellics Therapeutics $3.94 million to do what president and CMO Steve Chen calls “looking at traditional drug development upside down.”

Instead of going after a target directly — in this case bacterial toxins and inflammatory cytokines that cause sepsis — Cellics researchers “flip it around” to examine the host cells being attacked. The UC San Diego spinout then creates what it calls “nanosponges” — nanoparticles cloaked in the fragments of macrophage cell membranes. Chen says the “sponges” are designed to trap the sepsis-causing endotoxins and cytokines on their cell membranes, neutralizing them.

RBC's Bri­an Abra­hams holds a mock ad­comm on Bio­gen's iffy ad­u­canum­ab da­ta — and most of these ex­perts don't see a path to an ap­proval

As catalysts go, few loom larger than the aducanumab adcomm slated for Nov. 6.

With its big franchise under assault, Biogen is betting the ranch that its mixed late-stage Alzheimer’s data can squeak past the experts and regulators and get onto the market. And the topic — after a decade of Alzheimer’s R&D disasters in what still represents the El Dorado of drug markets — remains in the center ring of discussions around late-stage pipeline prospects.

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