Drug intelligence / Profile preview

QLS5132 + QL1706 + QL2107 + carboplatin + cisplatin + oxaliplatin

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

Overview

This combination therapy regimen is an investigational multi-agent protocol developed by Qilu Pharmaceutical for the treatment of advanced solid tumors, including ovarian, endometrial, gastric, and non-small cell lung cancers. The regimen centers on **QLS5132**, an antibody-drug conjugate (ADC) targeting **Claudin-6 (CLDN6)**, which is frequently upregulated in these tumor types. QLS5132 consists of a humanized anti-CLDN6 IgG1 antibody conjugated to a proprietary topoisomerase-1 inhibitor payload (QLS6916) via a hydrophilic cleavable linker. It is combined with **QL1706** (iparomlimab/tuvonivimab), a bifunctional antibody targeting PD-1 and CTLA-4, and **QL2107**, a monoclonal antibody targeting TIGIT. The regimen also incorporates platinum-based chemotherapy (carboplatin, cisplatin, or oxaliplatin) to enhance cytotoxic and immunogenic effects. This approach aims to leverage targeted ADC delivery, dual checkpoint blockade, and standard chemotherapy to overcome treatment resistance in CLDN6-positive malignancies.

02

Targets

CLDN6 (Claudin-6)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)DNAPDCD1 (Programmed cell death protein 1 receptor)TIGIT (T cell immunoreceptor with Ig and ITIM domains)

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