Clinical trial

A Phase II Clinical Study to Evaluate the Efficacy and Safety of QLS31905 and/or QL1706 Combination Chemotherapy for the Treatment of CLDN18.2-Positive Advanced Malignant Solid Tumors

Name
QLS31905-202
Description
This study aims to evaluate the efficacy and safety of QLS31905 and/or QL1706 plus chemotherapy in patients with Claudin18.2-positive advanced solid tumors.
Trial arms
Trial start
2024-06-30
Estimated PCD
2026-06-30
Trial end
2027-12-01
Status
Not yet recruiting
Phase
Early phase I
Treatment
QLS31905
Administered as an intravenous infusion.
Arms:
QLS31905 + gemcitabine+cisplatin, QLS31905 + gemcitabine+cisplatin+ QL1706, QLS31905 + oxaliplatin + capecitabine, QLS31905 + oxaliplatin + capecitabine + QL1706, QLS31905 + standard chemotherapy, QLS31905 + standard chemotherapy + QL1706
Oxaliplatin
130 mg/m2, intravenous infusion, D1, up to 8 cycles.
Arms:
QL1706 + oxaliplatin + capecitabine, QLS31905 + oxaliplatin + capecitabine, QLS31905 + oxaliplatin + capecitabine + QL1706
Capecitabine
1000 mg/m2, oral, bid, D1-D14
Arms:
QL1706 + oxaliplatin + capecitabine, QLS31905 + oxaliplatin + capecitabine, QLS31905 + oxaliplatin + capecitabine + QL1706
Gemcitabine
1000 mg/m2 administered as IV infusion on D1/D8 of each cycle.
Arms:
QL1706 + gemcitabine+cisplatin, QLS31905 + gemcitabine+cisplatin, QLS31905 + gemcitabine+cisplatin+ QL1706
Cisplatin
25 mg/m2, intravenous infusion, D1/D8, up to 8 cycles.
Arms:
QL1706 + gemcitabine+cisplatin, QLS31905 + gemcitabine+cisplatin, QLS31905 + gemcitabine+cisplatin+ QL1706
QL1706
5 mg/kg, intravenous infusion,D1
Arms:
QL1706 + gemcitabine+cisplatin, QL1706 + oxaliplatin + capecitabine, QL1706 + standard chemotherapy, QLS31905 + gemcitabine+cisplatin+ QL1706, QLS31905 + oxaliplatin + capecitabine + QL1706, QLS31905 + standard chemotherapy + QL1706
Chemotherapy drug
Standard chemotherapy recommended by guidelines.
Arms:
QL1706 + standard chemotherapy, QLS31905 + standard chemotherapy, QLS31905 + standard chemotherapy + QL1706
Size
360
Primary endpoint
Objective response rate (ORR)
Approximately 24 months
Eligibility criteria
Inclusion Criteria: * Subjects voluntarily participate in the study and sign the informed consent form; * Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1; * Expected survival time ≥ 3 months; * Histologically or cytologically confirmed locally advanced unresectable or metastatic solid tumors; * No prior systemic anti-tumor treatment for locally advanced unresectable or metastatic disease; * Tumor tissue samples determined to be positive for Claudin18.2 by immunohistochemistry (IHC); * At least one measurable lesion per RECIST v1.1; * Patients with adequate cardiac, liver, renal function, etc. Exclusion Criteria: * History of malignancies other than the target cancer within 5 years prior to the first dose of the investigational product ; * Underwent major organ surgery (excluding needle biopsy) or had significant trauma within 28 days prior to enrollment, or requires elective surgery during the study; * Known central nervous system metastases; * Patients with hepatitis B; patients with hepatitis C; patients who test positive for syphilis, or patients with a known history of HIV or positive HIV screening test; Patients with a known history of psychoactive drug abuse, alcohol abuse, or substance abuse; * Patients with added risks associated with the study or may interfere with the interpretation of study results as determined by the investigator, or deemed unsuitable by the investigator and/or sponsor.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 360, 'type': 'ESTIMATED'}}
Updated at
2024-06-06

1 organization

1 product

6 drugs

1 indication

Product
QLS31905
Drug
UTD1
Drug
QL1706
Drug
AN0025