Status:

COMPLETED

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

Lead Sponsor:

Jacobio Pharmaceuticals Co., Ltd.

Conditions:

Non-small Cell Lung Cancer

Colorectal Cancer

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief 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 anticipat...

Eligibility Criteria

Inclusion

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

Exclusion

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

Key Trial Info

Start Date :

September 26 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 16 2022

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT04045496

Start Date

September 26 2019

End Date

December 16 2022

Last Update

December 29 2025

Active Locations (4)

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Page 1 of 1 (4 locations)

1

HealthONE Clinic Services Oncology-Hematology

Denver, Colorado, United States, 80202

2

Tennessee Oncology, PLLC

Nashville, Tennessee, United States, 37203

3

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, United States, 77030

4

Washington University School of Medicine

Seattle, Washington, United States, 63110