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Onco-Innovations secures option on LAG-3 small-molecule program from Ifowonco

Onco-Innovations secures option on LAG-3 small-molecule program from Ifowonco

Calgary-based Onco-Innovations Limited (CBOE CA: ONCO / OTCQB: ONNVF) signed a non-binding letter of intent with Ifowonco Informatics Incorporated to negotiate an exclusive option covering Ifowonco's preclinical small-molecule LAG-3 inhibitor program, with the potential to obtain an exclusive worldwide license. Financial terms were not disclosed.

Under the proposed two-stage arrangement, Onco would first obtain an exclusive option to evaluate the LAG-3 program and, if the option is exercised, acquire an exclusive worldwide license. The transaction remains subject to negotiation and execution of a definitive agreement.

Ifowonco's program includes LG-306 and LG-310, small-molecule inhibitors of lymphocyte-activation gene 3 (LAG-3), an immune checkpoint receptor expressed on T cells. The compounds are being developed as orally available alternatives to biologic LAG-3 therapies, a class led by Bristol Myers Squibb's relatlimab, which is approved in combination with nivolumab. Ifowonco has reported in vitro activity for LG-306 and LG-310 and is continuing compound optimization and preclinical testing.

Onco said the program could also provide a potential combination strategy with ONC010, its nanoparticle-encapsulated polynucleotide kinase phosphatase (PNKP) inhibitor targeting the DNA damage response pathway. The company said DNA damage response inhibition and immune checkpoint blockade could represent complementary approaches, although no preclinical combination data were disclosed.

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The agreement would broaden Onco's pipeline beyond ONC010 as the company prepares its lead program for clinical development. In April 2026, Onco established an Australian subsidiary to support planned Phase I development under Australia's clinical trial notification framework and access local R&D tax incentives. ONC010 is advancing toward IND-enabling studies, with manufacturing and process-development activities underway.

Small-molecule approaches to LAG-3 remain at an early stage compared with antibody-based checkpoint inhibitors. Immutep Limited licensed a portfolio of small-molecule LAG-3 compounds from Cardiff University in 2024 for further optimization, while clinical development of LAG-3-targeted therapies has predominantly focused on biologics.


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