
Aktis Oncology was founded in 2020 to build a pipeline of targeted alpha radiopharmaceuticals. In October 2024, the company announced a $175 million Series B financing to advance its pipeline. In December 2025, Aktis filed for a U.S. initial public offering, and in January 2026 it disclosed an upsized IPO plan with Eli Lilly participating as an anchor investor.
Aktis focuses on oncology, specifically prevalent solid tumors where targeted delivery of an alpha-emitting radioisotope is intended to provide tumor-directed cytotoxicity. Current programs are positioned for indications that include urothelial carcinoma and multiple additional Nectin-4 or B7-H3–expressing tumor types.
Aktis develops miniprotein radioconjugates designed to deliver actinium-225 (Ac-225), an alpha-emitting radioisotope, to tumor-associated targets. The platform emphasis is on:
Matthew Roden, PhD serves as President and Chief Executive Officer.
Aktis has disclosed a 2024 partnership with Eli Lilly to develop tumor-targeting radiopharmaceuticals, alongside Lilly’s equity participation. The company has also established supply-chain planning typical for alpha-radiotherapy development, including radioisotope supply arrangements.
Aktis is developing targeted alpha radiopharmaceuticals using a miniprotein radioconjugate platform designed to deliver Ac-225 to tumor-associated targets in solid tumors.
Aktis is oncology-focused, targeting solid tumors selected on the basis of target expression (for example Nectin-4 and B7-H3 expression) and clinical need.
In December 2025, Aktis filed for a U.S. IPO. In January 2026, the company disclosed an upsized IPO plan with Eli Lilly as an anchor investor. Earlier, in October 2024, Aktis announced a $175 million Series B financing to advance its radiopharmaceutical pipeline.
Aktis has presented preclinical and translational work for AKY-1189, including development and dosimetry-related analyses, and has an ongoing Phase Ib study. Public updates to date emphasize trial initiation and scientific/technical readiness rather than mature clinical efficacy readouts.
Near-term milestones center on execution of the ongoing Phase Ib study for AKY-1189 and transition of AKY-2519 from IND-enabling work into clinical testing. As a radiopharmaceutical developer, key milestones also include dosimetry characterization and dose-optimization work to support later-stage study design.
Aktis is led by a CEO with experience spanning biopharma leadership and capital markets, supported by a team structured to advance radiopharmaceutical discovery, CMC, clinical development, and operational execution in multi-site oncology trials.
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