European biotech VC closes first fund with over $120M in the bank, thanks to big investors

Johan Kördel, Sound Bioventures founding partner

No­vo Hold­ings starts the new year off with a bang — right in­to a biotech VC’s first fund.

The firm an­nounced its undis­closed in­vest­ment — a ‘cor­ner­stone’ in­vest­ment, ac­cord­ing to No­vo — this morn­ing in­to Sound Bioven­tures Fund I, a fund ap­pro­pri­ate­ly man­aged by Sound Bioven­tures. The ven­ture cap­i­tal firm aims to in­vest one-third of its fund in Scan­di­na­vian biotechs, an­oth­er third in US and UK biotechs, and the fi­nal third in oth­er Eu­ro­pean biotechs out­side Scan­di­navia and the UK.

No­vo Hold­ings was joined by Sam­in­vest, Væk­st­fonden, Rams­bury In­vest and the Eu­ro­pean In­vest­ment Fund, along­side oth­er pri­vate in­vestors.

With all in­vest­ments so far at first close, Sound’s first fund has net the VC $124 mil­lion (or €110 mil­lion).

Found­ing part­ner Jo­han Kördel told End­points News that they hope to get to €150 mil­lion in the next 12 months, and have a hard cap of €200 mil­lion, or just un­der $250 mil­lion, if the fund is ‘ex­treme­ly suc­cess­ful.’

Sound has a three-man found­ing team. Casper Breum and Kördel, who spent 12 years to­geth­er at ma­jor VC Lund­beck­fonden be­fore go­ing off on their own to start Sound, are based in Eu­rope. And there’s a third man be­hind the cur­tain — Bib­hash Mukhopad­hyay.

Based out of Wash­ing­ton, DC, Mukhopad­hyay used to be a prin­ci­pal at NEA. He was brought on board with Sound at the rec­om­men­da­tion of Søren Møller, a man­ag­ing part­ner at No­vo Seeds, to bring on some­one in the US.

‘Møller made it clear to us that it’s go­ing to be chal­leng­ing for you to be fi­nan­cial­ly suc­cess­ful, if you on­ly in­vest in Scan­di­navia,’ Kördel said.

Kördel con­tin­ued:

And in the work we did with Lund­beck­fonden Ven­tures, we in­vest­ed half of our in­vest­ments in the US and half in Eu­rope — so we were al­ready very at­tuned to hav­ing an in­ter­na­tion­al view on where to in­vest in life sci­ence. And we were en­cour­aged by, okay, we re­al­ly shouldn’t be look­ing at this as an in­ter­na­tion­al fund, with some sim­i­lar­i­ties to what we had been do­ing be­fore. And then it be­came clear that we would ben­e­fit from hav­ing some­body in the US.

The VC’s fo­cus is on biotechs with can­di­dates in clin­i­cal or late pre-clin­i­cal stages — and pri­mar­i­ly with­in rare dis­eases. How­ev­er, Kördel not­ed that Sound is not a huge fund, so while the part­ners like gene ther­a­py and cell ther­a­py, the CMC costs would be way high­er com­pared to pro­teins and small mol­e­cules. Søren Møller of No­vo Seeds told End­points that No­vo en­gaged with Sound more di­rect­ly be­tween nine months and a year ago to get in­vest­ment un­der­way — but it was not the first time he had worked with the brains be­hind the op­er­a­tion at Sound. Kördel said that he had talked with Møller as far back as 2019 about strik­ing out on his own along­side Casper Breum, and Møller had been coach­ing them since the ear­ly stage of the Covid-19 pan­dem­ic.

And while Møller would not dis­close the amount that No­vo in­vest­ed in­to Sound, he did say that the in­vest­ment was more sub­stan­tial than sym­bol­ic — and in­dica­tive of a po­ten­tial long-term re­la­tion­ship.

‘When we launch or when we cor­ner­stone a new man­ag­er like this one, we def­i­nite­ly fore­see to par­tic­i­pate in the next fund and the next fund, so it’s a long term re­la­tion­ship,’ Møller said.

Their Staying Power Lies in their Patient-Centricity

Decentralized clinical trials (DCTs) were traditionally utilized in an isolated fashion prior to the COVID-19 pandemic. To continue their research within the constraints of the pandemic, sponsors and clinical investigators pivoted to a decentralized model out of necessity. At the onset, regulatory agencies offered some guidance on the digital approaches that are acceptable to ensure DCT approaches are applied in a way that maintains patient safety, as well as data quality and integrity.

For anyone who’s been following how the US government has been allocating and shipping supplies of its Covid-19 treatments over the past year, the news has shifted so many times that it can be difficult to keep track of what’s still being shipped and where.

More change is coming this week too, as HHS has now decided to re-start shipments of both Eli Lilly (bamlanivimab plus etesevimab) and Regeneron (casirivimab plus imdevimab) monoclonal antibody products after a short pause because neither product works against the new variant Omicron. Lilly’s combo also was halted last June due to the presence of other variants.

Kicking off 2022, hundreds of pharmaceuticals, including some blockbusters, saw their list prices rise by about 5% on average. But overall, net drug prices (cost after rebates) declined for the fourth year in a row, potentially complicating already stalled drug price reform efforts.

Among the drugs seeing new increases as of Jan. 1 are Gilead’s bevy of blockbuster HIV drugs.

Biktarvy, which pulled in more than $7 billion in worldwide sales in 2020, saw a 4.8% price increase in 2021, and now, another 5.6% increase in 2022, according to a new report from the nonprofit 46brooklyn Research.

All the big R&D trends are on display in this new, record-topping list of drug approvals for 2021. Plus one.

Add up everything OK’d from CDER and CBER, and you have 61 new drug approvals for last year, topping the 59 OKs that had tied a record in 2020. The dark days of the early 2000s are a distant memory now, with a host of hungry upstarts promising to make their own entries one day as Big Pharmas double down on innovation.

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Piramal CEO Peter DeYoung (Credit: Piramal Pharma Solutions via Youtube)

During a typically quiet holiday break in biotech, Piramal Pharma made some noise, and it’s starting off 2022 with yet another big announcement.

The CDMO will invest millions into creating a high-throughput screening facility that will enhance the already existing in vitro biology capabilities at its Ahmedabad, India drug discovery site. The new expansion is scheduled to go live in Q3 of this year, and couple its biology services with chemistry capabilities already in operation.

When the FDA lifted a clinical hold on Applied Therapeutics’ lead program in galactosemia last February, the New York biotech signaled that they were then on a smooth road toward an accelerated approval, with plans to file an NDA in the third quarter of 2021.

Regulators, though, apparently changed their mind.

Applied has decided to hold on submitting an NDA for AT-007 as a treatment for galactosemia, the company disclosed, following discussions with the FDA in which the agency indicated that ‘clinical outcomes data will likely be required for approval.’

Still recovering from a setback in its lead program, Ovid Therapeutics has turned to AstraZeneca for a suite of experimental epilepsy drugs.

Ovid is paying the Big Pharma partner $5 million in cash and $7.5 million in stock to access a library of early-stage small molecules targeting the KCC2 transporter, including lead candidate OV350. AstraZeneca stands to receive milestones adding up to more than $200 million and retains an option for a strategic collaboration.

Michel Vounatsos (Credit: World Economic Forum/Ciaran McCrickard)

As Biogen stares down an impending patent cliff for its spinal muscular atrophy blockbuster Spinraza, it’s betting $60 million that a new antisense oligonucleotide from Ionis will help keep the company’s lead in that space.

Building on a yearslong relationship with Ionis, Biogen plumped down $60 million just before the new year to secure commercial and development rights to BIIB115, a preclinical SMA drug looking to one-up Spinraza, the companies announced Tuesday. The latter raked in just over $2 billion last year (a slight decrease from the year before) but faces a patent expiration as early as 2023.

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Photo by Anthony Behar/Sipa USA)(Sipa via AP Images

Children between the ages of 12 and 15 years old are now eligible for a third dose of the Pfizer-BioNTech vaccine after the FDA authorized it Monday, as well as a third shot for those between 5 and 11 who are immunocompromised.

The FDA also shortened the time between the completion of a primary vaccine and a booster shot to five months for Pfizer’s jab, although Moderna’s booster interval remains at 6 months. The moves come as Omicron has ripped through the US, causing the number of positive cases to skyrocket.
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