pp-118 Solution for infusion

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Comments
Indication: Cutaneous T-cell lymphomas (CTCL), including Sézary syndrome and mycosis fungoides, particularly in relapsed/refractory patients expressing KIR3DL2 Clinical stage: Phase 2 completed Modality: Biologic (humanized IgG1 monoclonal antibody) Mechanism / Target: Targets KIR3DL2, an inhibitory receptor selectively expressed on malignant T cells in CTCL; induces tumor cell killing via antibody-dependent cellular cytotoxicity (ADCC) Route / form: Intravenous infusion Differentiation: First-in-class targeting of KIR3DL2, enabling biomarker-driven patient selection; demonstrates selective depletion of malignant T cells while sparing normal T-cell populations; favorable tolerability profile compared with conventional systemic therapies; positioned as a targeted therapy for advanced CTCL with high unmet need
Manufacturer #39106
Europe-based clinical-stage oncology biotech developing Rx therapeutic antibodies that engage the immune system against cancer. Pipeline includes proprietary clinical and preclinical candidates in cancers with high unmet need. Advances programs through licensing partnerships with major pharmaceutical companies; listed on regulated exchanges.
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