A Study of Q-1802 in Patients With Advanced Solid Tumors
Study Details
Study Description
Brief Summary
Q-1802 is a bispecific antibody targeting both the tumor-specific antigen Claudin 18.2 and the immune checkpoint PD-L1. This is a multi-center, single-arm, open-label design to evaluate the safety and tolerance of Q-1802 in patients with advanced solid tumors, together with an assessment of pharmacokinetic characteristics and efficacy. The study consisted of two compartments: the dose-exploration stage and the dose-extension stage.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Q-1802 Q-1802 dose exploration and Q-1802 dose extension |
Drug: Q-1802
Q-1802 will be administered intravenously.
|
Outcome Measures
Primary Outcome Measures
- Number of participants with dose limiting toxicities [28 days]
Incidence of dose limiting toxicities(DLTs). A DLT is defined as an adverse event or abnormal laboratory value assessed as unrelated to disease, disease progression, inter-current illness, or concomitant medications that occurs within the first treatment cycle with Q-1802.
Secondary Outcome Measures
- Plasma concentration (Cmax) [70 days]
Highest observed plasma concentration of Q-1802
- Time to achieve Cmax (Tmax) [70 days]
Time of highest observed plasma concentration of Q-1802
- Area under the plasma concentration-time curve (AUC) [70 days]
Area under the plasma concentration time curve of Q-1802
- PD-L1 receptor occupancy rate (RO) [70 days]
PD-L1 receptor occupancy rate (RO) on the surface of T lymphocytes in peripheral blood at different time points of Q-1802
- Number of participants with treatment-related adverse events(TRAE) [70 days]
TRAE is defined as the AEs that the casual relationship of the AE is ralated to Q-1802.
- Objective response rate (ORR) [70 days]
ORR is defined as proportion of participants with complete response, partial response (CR+PR).
- Progression-free survival (PFS) [70 days]
PFS is defined as the interval of time between the date of first treatment to the earliest date of disease progression or death which occurs first.
- Duration of response ( DCR ) [70 days]
DCR is defined as proportion of participants with complete response, partial response, stable disease (CR+PR+SD).
- Duration of response ( DOR ) [70 days]
DOR is defined as the time from the participant's initial objective response (CR or PR) to study drug therapy, to disease progression or death due to any cause, whichever occurs first
Eligibility Criteria
Criteria
Inclusion Criteria:
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Male or female, age ≥18 years and ≤75 years.
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Patients with at least one measurable lesion per RECIST (v1.1) (applicable to the dose-extension stage).
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Eastern Cooperative Oncology Group (ECOG) performance status score 0 or 1 at screening and no deterioration occurs within two weeks before enrollment.
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Life expectancy period ≥ 12 weeks.
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Patients who have sufficient baseline organ function and whose laboratory data meet the following criteria (receiving no treatment of blood transfusions, albumin, recombinant human thrombopoietin, or colony-stimulating factor within 14 days before the first dose of this study).
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Patients with advanced gastric mucinous adenocarcinoma, advanced ovarian mucinous carcinoma or other dominant tumors participating in the dose-extension stage must provide eligible tumor tissue samples for biomarker detection; if subjects agree, tumor tissue samples should also be provided during the dose-exploration stage.
Exclusion Criteria:
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Patients who have received any prior PD-1/PD-L1 antibody therapy (applicable to the dose-exploration stage).
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Patients with uncontrolled blood pressure (systolic blood pressure ≥ 150 mm Hg and/or diastolic blood pressure ≥ 100 mm Hg) or previous hypertensive crisis or hypertensive encephalopathy.
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Patients with active peptic ulcer, gastric outlet obstruction or persistent recurrent vomiting.
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Patients with a history of monoclonal antibody allergic reaction.
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Patients who are considered ineligible by the investigator due to any other severe, acute or chronic disease or other causes that the investigator considers could affect the patient's participation or assessment in the study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Beijing cancer hospical | Beijing | China | ||
| 2 | West China Second University Hospical, Sichuan University | Chengdu | China | ||
| 3 | Fudan University Shanghai Cancer Center | Shanghai | China | ||
| 4 | PKUCare Luzhong Hospital | Zibo | China |
Sponsors and Collaborators
- QureBio Ltd.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Qure-1802-101