A De-risked
Clinical Asset in a Large Market

Lixumistat has completed Phase 1 with a clean safety profile and is showing early efficacy in the Phase 1b/2a PDAC trial. ImmunoMet is raising to complete the PDAC study and initiate GBM studies.

~$39M​

Total Capital Raised, 2015–present

$10M

Current Raise Target

Founded 2015

Spin-off of Hanall Biopharma, Korea

Phase 2-Ready​

Lixumistat Asset Status

~$39M

Total Capital Raised, 2015–present

$10M

Current Raise Target

Founded 2015​

Spin-off of Hanall Biopharma, Korea

Phase 2-Ready

Lixumistat Asset Status

Why ImmunoMet, Why Now

Lixumistat is the only clinical-stage OxPhos inhibitor with demonstrated efficacy in pancreatic cancer. Phase 1 is complete with a well-characterised safety profile. Phase 1b/2a is active at MD Anderson with a 50% response rate at the recommended dose.


The current raise funds the path to proof of concept in PDAC and GBM — two data inflection points that position ImmunoMet for partnering, licensing, or a next funding round.

Phase 1 Status

Complete — Safety Profile Established

Published: Janku et al., Inv New Drugs, 2022

Phase 1b/2a Status

Active — 50% ORR, 80% DCR at RP2D

2015 to present

Next Indication

Glioblastoma — IND Preparation

Window-of-Opportunity + Phase 2 planned

Raise target $10M confirmed in session transcript. ~$39M total raised confirmed in investor deck. Hanall Biopharma origin confirmed in session transcript.

Interested in Learning More?

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