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CLN-049

Bispecific antibody · Immune activation, directed at FLT3 tyrosine kinase receptor (FLT3) and CD3 · developed by Cullinan Therapeutics

Phase 1 Most advanced trial
CGEM Developer
1 Registered trials

What is CLN-049?

CLN-049 is a humanized, Fc-silenced IgG1-based bispecific antibody that binds the FLT3 receptor tyrosine kinase on tumor cells and CD3 on cytotoxic T-lymphocytes. By bridging the two, it redirects T cells to kill FLT3-expressing cells. It is being studied in relapsed or refractory acute myeloid leukemia and myelodysplastic syndrome.

Summary written with AI from the sources listed at the end of this page.

At a glance

Drug type
Bispecific antibody
Targets
FLT3 tyrosine kinase receptor (FLT3), CD3
Mechanism
Immune activation, directed at FLT3 tyrosine kinase receptor (FLT3) and CD3
Pathways
T-cell mediated cytotoxicity of FLT3-expressing tumor cells
Therapy area
Oncology
Developer
Cullinan Therapeutics Inc. (CGEM)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 1

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT05143996 Phase 1 Relapsed/Refractory Acute Myeloid Leukemia (AML) Recruiting CGEM

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Myelodysplastic Syndrome (MDS)Relapsed/Refractory Acute Myeloid Leukemia (AML)

Other drugs acting on FLT3

Sources

Updated Oct 11, 2026. Something wrong or missing? Report it on the CGEM page.

Follow CGEM, the company behind CLN-049

See CGEM's upcoming FDA decisions, trial readouts, cash runway and dilution risk, updated every day from SEC, FDA and ClinicalTrials.gov filings.

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.