Last updated: March 11, 2024
Sponsor: Jiangsu Alphamab Biopharmaceuticals Co., Ltd
Overall Status: Completed
Phase
1
Condition
Breast Cancer
Stomach Cancer
Gastric Cancer
Treatment
KN026
Clinical Study ID
NCT03619681
KN026-CHN-001
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female subject >= 18 years and =<75 years.
- Histologically or cytologically confirmed, locally advanced unresectable or metastaticbreast cancer or gastric cancer.
- ECOG score 0 or 1.
- Life expectancy >3 months.
- According to the definition of RECIST1.1, the patient has at least one measurablelesion.
- Adequate organ function prior to start treatment with KN026.
- Able to understand, voluntarily participate and willing to sign the ICF.
- Subjects (women of child-bearing potential and males with fertile female partner) mustbe willing to use viable contraception method.
Exclusion
Exclusion Criteria:
- Accepted any other anti-tumor drug therapies within 4 weeks before fist dose.
- Accepted radiotherapy within 4 weeks before enrollment(Subjects are eligible, whichaccepted palliative therapies within 2 weeks before the first dose of KN026 forosseous metastatic and all the AEs recovered).
- An anthracyclines antibiotic treatment, such as doxorubicin (Adriamycin) was receivedexceeding 300 mg/m² within 90 days before first KN026 dosing, or other equivalent doseantharcyclines.
- Subjects are eligible with clinically controlled and stable neurologic function >= 4weeks, which is no evidence of CNS disease progression; Subjects with spinal cordcompression and cancerous meningitis are not eligible.
- Pregnant or nursing females;or intend pregnancy within this study period or within 6monthes after the end of this study.
- Has not recovered (ie, >Grade 1) from AEs except alopecia and anemia.
- History of immunodeficiency, including HIV positive or other acquired, congenitalimmunodeficiency disease, or a history of organ transplantation.
- Severe chronic and active infection, need to system antibiosis/antiviral treatment.
- Cavity effusion (pleural effusion, ascites, pericardial effusion, etc.) are not wellcontrolled, and need locally treatment or repeated drainage. -
Study Design
Total Participants: 63
Treatment Group(s): 1
Primary Treatment: KN026
Phase: 1
Study Start date:
September 17, 2018
Estimated Completion Date:
August 26, 2022
Connect with a study center
Fudan University Shanghai Cancer Hospital
Shanghai, 200000
ChinaSite Not Available

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