A First-in-Human, Phase 1 Study of JAB-3312 in Adult Patients With Advanced Solid Tumors

Last updated: March 13, 2022
Sponsor: Jacobio Pharmaceuticals Co., Ltd.
Overall Status: Active - Recruiting

Phase

1

Condition

Breast Cancer

Colorectal Cancer

Pancreatic Cancer

Treatment

N/A

Clinical Study ID

NCT04045496
JAB-3312-1001
  • Ages > 18
  • All Genders

Study Summary

This is a Phase 1, first-in-human, open-label dose-escalation study to determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) and assess the DLT of JAB-3312. It is anticipated that approximately 24 subjects will be enrolled in the dose-escalation phase of the study. JAB-3312 will be administered orally once daily (QD) in 21-day treatment cycles.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Subject must be ≥18 years-of-age at the time of signature of the informed consent form (ICF).
  2. Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
  3. Subjects with histologically or cytologically confirmed advanced solid tumors whichhave progressed despite standard therapy or for which no standard therapy exists.
  4. Subjects with life expectancy ≥3 months.
  5. Patients must have at least one measurable lesion as defined by RECIST v1.1.
  6. Patients who have sufficient baseline organ function.

Exclusion

Exclusion Criteria:

  1. Severe autoimmune disease (including immune-related adverse events of priorimmune-oncology therapy) or autoimmune disorder that requires chronic systemiccorticosteroid treatment at immunosuppressive doses (prednisone >10 mg/day orequivalent).
  2. Known malignant central nervous system disease other than neurologically stable,treated brain metastases.
  3. History or evidence of interstitial lung disease, radiation pneumonitis which requiredsteroid treatment, or idiopathic pulmonary fibrosis, pleural or pericardial effusionthat required intervention such as a drain.
    1. History of seropositive status for hepatitis B, hepatitis C and humanimmunodeficiency virus (HIV).
  4. History or evidence of active infections (Grade ≥2).
  5. History or evidence of significant inflammatory or vascular eye disorder.
  6. History of an allogeneic bone marrow or solid organ transplant.
  7. Use of systemic anti-cancer agent (except for anti-androgen therapy for prostatecancer) or investigational drug ≤28 days prior to the first dose of JAB-3312.
  8. History of radiation therapy ≤28 days prior to the first dose of JAB-3312, or likelyto require radiation therapy at any time until the 30 days after the last dose ofJAB-3312.
  9. History of transfusion of whole blood, red blood cell or platelet packets ≤2 weeksbefore the start of treatment.
  10. Subjects experiencing unresolved Grade >1 toxicity before the start of treatment.

Study Design

Total Participants: 24
Study Start date:
September 26, 2019
Estimated Completion Date:
March 31, 2024

Connect with a study center

  • HealthONE Clinic Services Oncology-Hematology

    Denver, Colorado 80202
    United States

    Active - Recruiting

  • Tennessee Oncology, PLLC

    Nashville, Tennessee 37203
    United States

    Active - Recruiting

  • The University of Texas M. D. Anderson Cancer Center

    Houston, Texas 77030
    United States

    Active - Recruiting

  • Washington University School of Medicine

    Seattle, Washington 63110
    United States

    Active - Recruiting

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