This Study is to Evaluate Safe and Effective Treatment Dose of OBI-888 in Patients With Locally Advanced or Metastatic Solid Tumors.

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

54

Participants

Timeline

Start Date

May 7, 2018

Primary Completion Date

April 7, 2022

Study Completion Date

April 7, 2022

Conditions
Metastatic Solid TumorsLocally Advanced Solid Tumors
Interventions
DRUG

OBI-888

For the dose-escalation phase, OBI-888 will be given weekly at the dose levels of 5, 10, and 20 mg/kg.

DRUG

OBI-888

For the dose-expansion phase, OBI-888 will be given weekly at 20 mg/kg dose level.

DEVICE

Globo H IHC Assay

This assay will be used to identify eligible patients who may clinically benefit from the OBI-888 treatment, defined by Globo H expression.

Trial Locations (9)

704

National Cheng Kung University Hospital, Tainan City

11217

Taipei Veterans General Hospital, Taipei

38138

West Cancer Center and Research Institute, Germantown

40447

China Medical University Hospital, Taichung

77030

MD Anderson Cancer Center, Houston

90033

USC/Norris Comprehensive Cancer Center, Los Angeles

92037

Scripps Clinic Torrey Pines, La Jolla

92663

Hoag Memorial Hospital Presbyterian, Newport Beach

08903

Rutgers Cancer Institute of New Jersey, New Brunswick

Sponsors

Lead Sponsor

All Listed Sponsors
lead

OBI Pharma, Inc

INDUSTRY

NCT03573544 - This Study is to Evaluate Safe and Effective Treatment Dose of OBI-888 in Patients With Locally Advanced or Metastatic Solid Tumors. | Biotech Hunter | Biotech Hunter