Drug intelligence / Profile preview

QLS5132 + QL1706 + QL2107

Development stage
Unknown
Lead developer
Qilu Pharmaceutical
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

QLS5132 + QL1706 + QL2107 is an investigational combination therapy regimen developed by Qilu Pharmaceutical for the treatment of advanced solid tumors, specifically those expressing Claudin-6 (CLDN6). The regimen integrates three distinct therapeutic modalities: QLS5132, an antibody-drug conjugate (ADC) targeting CLDN6 with a topoisomerase-1 inhibitor payload; QL1706 (iparomlimab/tuononlimab), a bifunctional antibody that simultaneously blocks the PD-1 and CTLA-4 immune checkpoints; and QL2107, a monoclonal antibody targeting the TIGIT checkpoint. By combining targeted cytotoxic delivery with multi-pathway immune checkpoint inhibition, this regimen aims to enhance anti-tumor efficacy and overcome immune evasion in cancers such as gastric, non-small cell lung, endometrial, and ovarian cancer. It is currently being evaluated in a Phase Ib/II clinical trial to assess safety, tolerability, and preliminary efficacy.

02

Targets

CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)PDCD1 (Programmed cell death protein 1 receptor)CLDN6 (Claudin-6)

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