A Clinical Study of AL2846 Capsule Combined With Gemzar Injection in the Treatment of Advanced Pancreatic Cancer

NCT ID: NCT06278493

Last Updated: 2024-02-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-08-23
• Study Completion Date: 2023-05-01

Brief Summary

This is a clinical study to observe the tolerance and primary efficacy of AL2846 capsules combined with Gemzar injection in patients with pancreatic cancer, and to determine the recommended dosage and administration method for subsequent clinical studies.

Conditions

Pancreatic Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

AL2846 capsules + Gemzar injection

AL2846 capsules combined with Gemzar injection,28 days as a treatment cycle

Group Type: EXPERIMENTAL

AL2846 capsules

Intervention Type: DRUG

AL2846 is a multi -target receptor tyrosine kinase inhibitor.

Gemzar

Intervention Type: DRUG

It is a chemotherapeutic drug.

Interventions

AL2846 capsules

AL2846 is a multi -target receptor tyrosine kinase inhibitor.

Intervention Type: DRUG

Gemzar

It is a chemotherapeutic drug.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Non operative patients with pancreatic cancer confirmed by histology or cytology, At least one evaluable lesion exists.
• ≥18 years old and ≤70 years old, Eastern Cooperative Oncology Group (ECOG) Performance Status: 0-1, expected survival period of more than 3 months.
• No chemotherapy or targeted treatment has been carried out for advanced pancreatic cancer, or more than half a year after the end of postoperative treatment.
• Normal function of major organs.
• Female subjects should agree to use contraception during the study period and within 6 months after the end of the study; Within 7 days prior to enrollment in the study, the serum or urine pregnancy test should be negative and must be a non lactating patient; Male subjects should agree to use contraceptive measures during the study period and within 6 months after the end of the study period.
• Subjects voluntarily participate in this study and sign informed consent.

Exclusion Criteria

• Have any type of active malignant tumor or have a history of malignant tumor.
• Previously treated with Gemzar injection.
• Known brain metastases, spinal cord compression, cancerous meningitis, or diseases of the brain or pia mater detected during Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) screening.
• Clinically significant ascites in patients.
• Diarrhea greater than or equal to level 2.
• Have any acute or chronic active infectious disease.
• Hypertensive patients who cannot be well controlled, or suffering from myocardial ischemia or myocardial infarction, arrhythmia, and grade I heart failure.
• Urine routine indicates urine protein ≥++, and it is confirmed that the 24-hour urine protein quantification is greater than 1.0 g.
• History of abdominal fistula, gastrointestinal perforation, or abdominal abscess within 6 months.
• Long term unhealed wounds or fractures.
• Individuals who have experienced arterial/venous thrombosis events within 6 months, such as cerebrovascular accidents (including temporary ischemic attacks), deep vein thrombosis, and pulmonary embolism.
• Patients treated with anticoagulants or vitamin K antagonists such as warfarin, heparin, or their analogues; Under the premise that international normalized ratio (INR) is ≤ 1.5, it is allowed to use low-dose warfarin (1mg orally, once daily) or low-dose aspirin (not exceeding 100mg daily) for preventive purposes.
• Individuals with a history of psychiatric drug abuse who are unable to quit or have mental disorders.
• Patients known to be allergic to Gemzar injection.
• Patients with active hepatitis B or hepatitis C.
• Individuals with a history of immunodeficiency, including HIV testing positive or other acquired or congenital immunodeficiency diseases, or a history of organ transplantation.
• According to the investigator's judgment, there are accompanying diseases that seriously endanger patient safety or affect the completion of the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Tianjin Medical University Cancer Hospital

Tianjin, Tianjin Municipality, China

Countries

China

Other Identifiers

AL2846-I-0002

Identifier Type: -

Identifier Source: org_study_id