Latest News

29 June 2026

HaemaLogiX Board Update

HaemaLogiX Ltd, a clinical-stage biotech developing novel immunotherapies for patients with blood cancers and B cell diseases, today announces a planned transition in its Board, with Dr John Cullity stepping down as Non-Executive Chair after 12 years of service. The Board has appointed co-founder Alan Liddle as incoming Non-Executive Chair.

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18 June 2026

HaemaLogiX Receives Ethics Approval for KappaMab™ Phase 2b Trial in Patients with Relapsed, Kappa-Restricted Multiple Myeloma

HaemaLogiX Ltd, a clinical-stage biotech developing novel immunotherapies for patients with blood cancers and B cell diseases, is pleased to announce that it has received approval from the Human Research Ethics Committee (HREC) at the Alfred Hospital Ethics Committee (Bayside Health) for the Phase 2b clinical trial of its lead asset, KappaMab™.

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19 May 2026

KOALA Trial Reaches Major Milestone with Commencement of Patient Enrolment

HaemaLogiX Ltd is pleased to announce that the KOALA Phase 1 clinical trial is now active and open to patient enrolment at the Peter MacCallum Cancer Centre. The study targets multiple myeloma, the second most common blood cancer worldwide.

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15 May 2026

Scrip Article: With Selective Targeting, HaemaLogiX Eyes Crowded Multiple Myeloma Space

HaemaLogiX is gearing up for an initial public offering (IPO) this year, hoping that market proceeds can help accelerate a second Phase IIb trial of a monoclonal antibody targeting Kappa myeloma antigen – a largely untouched target in an increasingly competitive multiple myeloma (MM) market.

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14 May 2026

Drug Discovery World: Redefining targeted immunotherapy in multiple myeloma through antigen innovation

The core breakthrough is the discovery of two novel tumour-specific antigens. HaemaLogiX has identified Kappa Myeloma Antigen (KMA) and Lambda Myeloma Antigen (LMA) — conformational, lipid-associated epitopes that arise when free light chains bind sphingomyelin within the malignant plasma cell membrane, expressed only on cancerous plasma cells and absent from normal bone marrow plasma cells.

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