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Lenzilumab (LENZ)

Chronic Myelomonocytic Leukemia (CMML)

Phase 2/3Active

Key Facts

Indication
Chronic Myelomonocytic Leukemia (CMML)
Phase
Phase 2/3
Status
Active
Company

About Taran Therapeutics

Taran Therapeutics is a clinical-stage biotech developing lenzilumab, a monoclonal antibody targeting GM-CSF to treat serious myeloid leukemias and inflammatory conditions. Its lead program is in a fully enrolled Phase 2/3 trial for high-risk CMML, demonstrating an 80% clinical response rate when added to standard of care, significantly outperforming current treatments. The company is also advancing LENZ for secondary AML, MDS, and to mitigate CAR-T therapy toxicities, with a Phase 3 protocol for the latter indication agreed with the FDA. Taran is privately held and preparing for regulatory discussions to chart a path to potential marketing approval.

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About Taran Therapeutics

Taran Therapeutics is a clinical-stage biotech developing lenzilumab, a monoclonal antibody targeting GM-CSF to treat serious myeloid leukemias and inflammatory conditions. Its lead program is in a fully enrolled Phase 2/3 trial for high-risk CMML, demonstrating an 80% clinical response rate when added to standard of care, significantly outperforming current treatments. The company is also advancing LENZ for secondary AML, MDS, and to mitigate CAR-T therapy toxicities, with a Phase 3 protocol for the latter indication agreed with the FDA. Taran is privately held and preparing for regulatory discussions to chart a path to potential marketing approval.

View full company profile

About Taran Therapeutics

Taran Therapeutics is a clinical-stage biotech developing lenzilumab, a monoclonal antibody targeting GM-CSF to treat serious myeloid leukemias and inflammatory conditions. Its lead program is in a fully enrolled Phase 2/3 trial for high-risk CMML, demonstrating an 80% clinical response rate when added to standard of care, significantly outperforming current treatments. The company is also advancing LENZ for secondary AML, MDS, and to mitigate CAR-T therapy toxicities, with a Phase 3 protocol for the latter indication agreed with the FDA. Taran is privately held and preparing for regulatory discussions to chart a path to potential marketing approval.

View full company profile

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