A First-in-Human Study of JAB-3068 (SHP2 Inhibitor) in Adult Patients With Advanced Solid Tumors in China
About the study
This is a Phase 1/2a, open-label, multi-center study of JAB-3068 in Patients with advanced solid tumors.This study has two phases: dose escalation phase and dose expansion phase.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Written informed consent obtained prior to any study-related procedure being performed;
- Age 18 years or older;
- Dose escalation(phase I): Patients with histologically or cytologically confirmed, advanced solid tumors (including lymphoma) which have progressed from standard therapy or for whom no standard therapy exists; Dose expansion(phase IIa ): Patients with histologically or cytologically confirmed, advanced NSCLC, ESCC, HNSCC which have progressed from standard therapy;
- Patients with life expectancy ≥3 months;
- Dose expansion(phase IIa ): patients have available archival tissue can be provided or willing to perform biopsy to provide fresh tumor tissue.
- Patients with other solid tumors must have at least one measurable lesion as defined by RECIST v1.1;Patients with Lymphomas must have at least one measurable lesion as defined by IWG 2007 criteria;
- Eastern Cooperative Oncology Group performance score 0 or 1;
- Patients who have sufficient baseline organ function.
EXCLUSION CRITERIA
Exclusion Criteria:
- Patients with life-threatening autoimmune disease or with autoimmune disorder and who are on long-term steroid treatment;
- History or current evidence of retinal vein occlusion (RVO) or current risk factors for RVO;
- Lymphoma with brain metastasis; Other solid tumors:Known malignant central nervous system (CNS) disease other than neurologically stable, treated brain metastases;
- Active infection including hepatitis B, hepatitis C and human immunodeficiency virus (HIV)
- Patients who have any severe and/or uncontrolled medical conditions or other conditions that, in the opinion of the Investigator and Sponsor, could affect the patient's participation in the study
- Patients who have impaired cardiac function or clinically significant cardiac diseases
- Use of anti-cancer treatment drug ≤21 days prior to the first dose of JAB-3068.
- Use of an investigational drug during the past 30 days prior to the first dose of JAB-3068.
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Non-small Cell Lung Cancer,Head and Neck Cancer,Esophageal Cancer,Other Metastatic Solid Tumors
Age (in years)
18+
Phase
Phase 1/Phase 2
Participants needed
120
Est. Completion Date
Sep 30, 2022
Treatment type
Interventional
Sponsor
Jacobio Pharmaceuticals Co., Ltd.
ClinicalTrials.gov identifier
NCT03565003
Study number
JAB-3068-02
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