Seattle biotech Cyrus Biotechnology announced this morning that it closed an $18 million Series B — and landed an acquisition to boot.
The biotech, which has an in-house software program for biologics discovery, acquired Orthogonal Biologics, a spin-out from the University of Illinois that focuses on using ‘Big Data’ to run deep mutational scanning on proteins and receptors for drug discovery.
The financing includes investments from OrbiMed Advisors, Trinity Ventures, Agent Capital, Yard Ventures, among others. And Selecta Bioscience, with which Cyrus is already working on autoimmunity programs, joined as a strategic investor.
The plan, for the two companies? Merge and move into drug discovery.
‘We are thrilled to bring together a range of experienced biotech investors from across the globe to support our move into independent drug discovery,’ said Cyrus CEO Lucas Nivon.
‘By merging our company with Cyrus, we can create a unified biologics discovery platform,’ former Orthogonal CEO Erik Procko added. — Paul Schloesser
Another George Church alum launches a biotech startup — matching AI for protein drug development
AI remains one of the big emerging sectors in the biopharma industry, as new players continue to push to compete for what they see as the future of drug development.
Today it was Surge Biswas’ turn at bat, picking up an $11 million seed round for a Boston-based startup called Nabla Bio. Khosla Ventures and Zetta Venture Partners led the startup raise, with participation from Fifty Years, Cantos Ventures and others.
That money will be put to use developing what the biotech calls ‘an AI-first protein design platform, enabling rapid end-to-end engineering of next-generation antibody therapeutics.’
‘Therapeutic antibody design is not just about binding to targets, and insufficient protein engineering is estimated to be responsible for a large fraction of clinical trial discontinuations and failures, especially for large molecule biologics that will play an increasingly prominent role in the clinic,’ said Alex Morgan, a partner at Khosla Ventures. ‘As therapeutics become more complex with more functional domains, the role of AI in development will become critical.’ — John Carroll
AbbVie’s PhIII induction study reaches both primary endpoints in Crohn’s disease patients
As a drug class, JAK inhibitors have been rife with concerns of safety — but AbbVie’s latest study on JAK inhibitor upadacitinib, aka Rinvoq, may quell some of those concerns.
The pharma announced this morning that a Phase III trial in patients with Crohn’s disease reached both primary endpoints: clinical remission and endoscopic response after 12 weeks.
The double-blind, placebo-controlled trial known as U-EXCEED is the first of two Phase III induction studies to evaluate safety and efficacy of Rinvoq in adults with moderate to severe Crohn’s disease.
Full results from the study will be presented at upcoming medical conferences and published in a peer-reviewed medical journal.
‘I am thrilled to see the results of this first Phase III induction study of upadacitinib,’ said Jean-Frederic Colombel, one of the U-EXCEED study investigators and director of the Inflammatory Bowel Disease Center at Mount Sinai. — John Carroll
https://endpts.com/seattle-biotech-closes-18m-series-b-and-acquires-a-company-another-george-church-alum-launches-upstart/