Aerska's series A triples funds for brain delivery of RNAiGalux bags $29M for AI protein designVesalic claims ALS target breakthrough in debutCSL bets on Memo's polyclonal IgG techAerska's series A triples funds for brain delivery of RNAiAerska, which emerged from stealth last October with $21 million in seed funding, has now raised another $39 million via a series A round, bringing its total capital to $60 million. The latest financing was led by EQT Dementia Fund and age1, with participation from Iaso Ventures, as well as existing investors.Proceeds from the financing will be used to advance Aerska's brain shuttle technology to improve delivery of RNAi therapeutics across the blood-brain barrier to treat neurological diseases. The biotech's antibody-oligo conjugate (AOC) platform is progressing towards the clinic.As part of the series A financing, EQT'S Arno de Wilde and Philip Scheltens, along with Alex Colville from age1, will join Aerska's board.-Matthew DennisGalux bags $29M for AI protein designAfter securing a protein design deal with Boehringer Ingelheim last year, South Korean biotech Galux has now raised a $29-million series B to advance its AI platform and build out its R&D infrastructure. The financing adds to an $18-million series A closed in 2022, bringing the firm's total funding to $47 million.The company's protein-focused GaluxDesign technology specialises in de novo antibody design across a range of therapeutic targets, including G protein-coupled receptors and ion channels. By integrating AI with wet lab–generated experimental data, Galux believes its platform can generate precise, consistent antibody structures.Existing backers InterVest, DAYLI Partners and PATHWAY Investment participated in the round alongside new investors including Yuanta Investment, Korea Development Bank, SL Investment, NCORE Ventures, SneakPeek Investments, Korea Investment & Securities and Mirae Asset Securities.-Elizabeth EatonVesalic claims ALS target breakthrough in debutEmerging from stealth on Monday, Vesalic is advancing both therapeutic and diagnostic technologies for amyotrophic lateral sclerosis (ALS) that build upon the discovery of a new driver of ALS and other motor neuro diseases (MNDs) that's largely external to the brain and central nervous system (CNS).While Vesalic is keeping the biological specifics close to its chest, the newco said it's targeting a toxic exosome cargo in ALS patients created via a newly discovered systemic metabolic dysfunction. The company plans to "intercept and neutralise" the toxins before they're carried to the CNS, where they bind to and damage neurons — potentially slowing or halting progression of both the monogenic and sporadic forms of ALS. The startup is running in vivo studies and plans to submit regulatory filings in 2027 to move its candidate into the clinic. Along with the novel target, Vesalic has identified a blood-based disease signature it thinks could predict ALS years before a patient is symptomatic. -Elizabeth EatonCSL bets on Memo's polyclonal IgG tech CSL entered into a collaboration with Swiss biotech Memo Therapeutics to advance the latter's recombinant polyclonal IgG technology. Michael Wilson, senior VP of global research at CSL, said the partnership will help "explore new treatment options for people with rare and serious diseases."Under terms of the deal, Memo will use its DROPZYLLA platform to develop recombinant polyclonal IgG products, with CSL holding an exclusive option to license. In return, Memo stands to receive exploratory R&D funding and access to technology, and — if the option is exercised — a licence fee plus milestone payments totalling up to CHF 265 million ($328 million) on the first product, alongside single-digit sales royalties.-Pavan Kamat