Trial of KN026 in Patients With HER2-positive Advanced Malignant Breast Cancer and Gastric Cancer

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

This is a first-in-human (FIH), open-label, phase 1 dose-escalation study of KN026 in subjects with HER2 positive advanced breast and Gastric Cancer. The standard "3 + 3" design was used for dose escalation. There are 5 proposed dose levels which are 5, 10, 15, 20 and 30 mg/kg, but dosing interval may be adjusted during the study (such as QW, OR Q2W, OR Q3W) based on emerging data from this trial and/or from phase 1 trial of KN026 in other country. Dose escalation will continue until the maximum tolerated dose (MTD) is reached or if MTD is not found, dose escalation will continue until the MAD of 20 mg / kg is reached. Dose expansion will carried out in 20 mg/kg Q2W and 30 mg/kg Q3W.

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
    China

    Site Not Available

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