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Nov 6, 2026M&A

Acrivon acquires JAK1 inhibitor ACR-525 from Aqilion, enters immunology

Acrivon Therapeutics paid cash for a Phase 2-ready oral JAK1 inhibitor and a preclinical PKCθ program, establishing immunology and inflammation as a new pillar alongside oncology.

Acrivon Therapeutics announced on November 6, 2026 that it had acquired ACR-525 (formerly known as AQ280), a Phase 2-ready, oral, highly selective Janus kinase 1 (JAK1) inhibitor, and a protein kinase C theta (PKCθ) inhibitor preclinical program, from Aqilion AB.1 The company said the acquisition establishes immunology and inflammation as a strategic pillar for Acrivon alongside its oncology programs.1

Under the deal terms, Acrivon acquired Aqilion's rights to AQ280 (now known as ACR-525) and the PKCθ inhibitor preclinical programs, including the associated intellectual property rights, data, regulatory filings and drug supply, for an undisclosed cash consideration without future royalties or milestone obligations.1 Separately, Acrivon, Aqilion and LEO Pharma entered into an agreement terminating all future royalty and milestone obligations on ACR-525 previously agreed to between Aqilion and LEO Pharma.1 The transaction was approved by the boards of directors of Acrivon and Aqilion and closed concurrently with the signing of the definitive agreement.1

Acrivon said that as part of due diligence, it applied global AP3 phosphoproteomic profiling to quantify ACR-525's drug-regulated cellular pathway effects against six approved JAK inhibitors and dupilumab, characterizing ACR-525 as a highly selective JAK1 inhibitor with minimal off-target effects compared to approved JAK inhibitors and broader cellular effects than dupilumab.1

For initial development, based on two completed Phase 1 studies, and a formulation designed for patients with difficulty swallowing, EoE is targeted as first potential indication.1 The company also noted potential in other areas, since given its high selectivity and oral availability, ACR-525 has potential in IBD and other immune disorders, both as a single agent and in combination with approved I&I therapies.1

Acrivon plans to host a webcast with EoE Key Opinion Leaders to discuss the ACR-525 and PKCθ inhibitor preclinical programs on November 10, 2026, at 4:00 p.m. ET.1 Expected participants include Evan Dellon, M.D., M.P.H. of the University of North Carolina at Chapel Hill and Arjan Bredenoord, Ph.D. of Amsterdam University Medical Center.1

Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.