QL1604 Monotherapy for dMMR or MSI-H Advanced Solid Tumors

Advanced Malignant Tumor Clinical Trial

Official title:

A Single-arm, Multi-center, Phase Ⅱ Clinical Study to Evaluate Efficacy and Safety of QL1604 Monotherapy for the Treatment of Unresectable or Metastatic Mismatch Repair Deficient (dMMR) or Microsatellite Instability-high (MSI-H) Solid Tumors That Failed to Respond to Standard Therapy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04326829
• Other study ID #: QL1604-201
• Status: Recruiting
• Phase: Phase 2
• Start date: July 8, 2020
• Est. completion date: July 2023

Study information

• Verified date: November 2022
• Source: Qilu Pharmaceutical Co., Ltd.
• Contact: Shunjiang Yu, CMO
• Phone: 0531-83129659
• Email: shunjiang.yu[@]qilu-pharma.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this study, patients with previously-treated locally-advanced or metastatic mismatched repair deficient (dMMR) or microsatellite instability-high (MSI-H) colorectal carcinoma (CRC) and other solid tumors will be treated with QL1604 monotherapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 86
• Est. completion date: July 2023
• Est. primary completion date: December 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Volunteer to participate in this clinical study; completely understand and know this study as well as sign the informed consent form (ICF);

2. Age = 18 years and = 80 years when ICF is signed;

3. Histologically confirmed locally advanced or metastatic dMMR or MSI-H status colorectal carcinoma or other malignant solid tumors;

4. At least one measureable lesion as defined per RECIST Version (v) 1.1 ;

5. Subjects who have disease progression or intolerable reactions after the currently available standard anti-cancer treatment previously received or refused prior cancer therapy regimen(s) ;

6. Subjects must provide tumor tissues and blood samples for the determination of MSI, tumor mutational burden (TMB), PD-L1 expression level;

7. Eastern Cooperative Oncology Group performance status of 0 or 1;

8. Life expectancy of greater than 12 weeks;

9. Adequate hematologic and organ function;

10. Female subjects who are not pregnant or breastfeeding

11. Male and female subjects able to have children must agree to use highly effective method of contraception throughout the study and for at least 120 days after last dose.

Exclusion Criteria:

1. Known hypersensitivity to any monoclonal antibody, QL1604 and/or any of its excipients;

2. Subjects with known central nervous system (CNS) metastasis;

3. Active autoimmune disease that has required systemic treatment in past 2 years, replacement therapy is acceptable;

4. Subjects with major cardiovascular and cerebrovascular diseases;

5. Subjects with uncontrollable pleural effusion, pericardial effusion or ascites;

6. Any condition that required systemic treatment with either corticosteroids (> 10 mg daily of prednisone or equivalent) or other immunosuppressive medication = 14 days before the first dose of study drug;

7. Subjects who have received surgery, radiotherapy, chemotherapy, targeted therapy, other anti-tumor treatments, or participating in other clinical studies is less than 4 weeks before the first administration of investigational product;

8. Subjects who have not recovered to CTC AE Grade 1 or better from related side effects of any prior antineoplastic therapy;

9. Received a live vaccine within 30 days of planned start of study medication;

10. Infection with human immunodeficiency virus (HIV), HAV, HBV and HCV;

11. Prior therapy with an anti-programmed cell death (PD)-1, anti-PD-ligand 1 (anti-PD-L1), anti-PD-L2 agent, cytotoxic lymphocyte associated protein-4 (CTLA-4), OX-40, CD137;

12. Known psychiatric or substance abuse disorders that would interfere with the requirements of the study;

13. History or current evidence of any condition, therapy, or laboratory abnormality, that might confound the results of the trial, or interfere with the participant's participation for the full duration of the study, or investigators/sponsor consider the subjects are not suitable for this trial.

Related Conditions & MeSH terms

• Advanced Malignant Tumor
• Neoplasms

Intervention

Drug:
• QL1604
QL1604, IV infusion

Locations

Country	Name	City	State
China	West China Hospital, Sichuan University	Chengdu	Sichuan
China	Fudan University Cancer Hospital	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Qilu Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	ORR	Objective response rate (assessed by independent radiological review committee (IRRC) per RECIST Version 1.1 and iRECIST)	up to 2 years
Secondary	ORR	Objective response rate (assessed by the investigators per RECIST Version 1.1 and iRECIST)	up to 2 years
Secondary	6-month PFS rate	6-month progression-free survival (PFS) rate	the proportion of subjects who have time interval over 6 months between the first dose and disease progression or death
Secondary	6-month OS rate	6-month overall survival rate	from the date of first dose until the date of 6-month
Secondary	PFS	Progression-free survival (assessed by independent radiological review committee (IRRC) per RECIST v1.1 and iRECIS)	from the first dose until firstly confirmed and recorded disease progression or death (whichever occurs earlier), assessed up to 2 years
Secondary	PFS	Progression-free survival (assessed by the investigators per RECIST v1.1 and iRECIST)	from the first dose until firstly confirmed and recorded disease progression or death (whichever occurs earlier), assessed up to 2 years
Secondary	OS	Overall survival	from the date of first dose until the date of death from any cause, assessed up to 2 years
Secondary	DOR	Duration of response	from the date when CR or PR (whichever recorded earlier) is firstly achieved until the date when disease progression or death is firstly recorded (whichever occurs earlier), assessed up to 2 years