Safety and Biomarker of OPB-111077 in Subjects With Advanced Solid Tumor

NCT ID: NCT02250170

Last Updated: 2019-09-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 47 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-10-23
• Study Completion Date: 2019-03-08

Brief Summary

This open-label, non-randomized trial will comprise of 2 parts. A dose escalation part will characterize the safety, biomarker and pharmacokinetics of OPB-111077 in advanced solid tumor. Subsequently, an expansion part will further evaluate the biomarker, safety, pharmacokinetics and antitumor activity of OPB-111077 in selected tumor types.

Detailed Description

This trial is designed to determine the safety, tolerability, maximum tolerated dose and recommended dose of OPB-111077 administered orally 4-days on and 3-days off (3 weeks/cycle) to subjects with advanced solid tumor in the dose escalation part so that biomarkers, efficacy, and others can be evaluated at the recommended dose in an expeditious manner in the expansion part. The dose escalation part employs a 3+3 escalation design as a standard dose escalation design for a small sample size.

Conditions

Solid Tumor

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

OPB-111077

Tablet, Oral, 300mg/500mg/700mg/900mg 4 days-on \& 3 days-off (21 days=1cycle)

Group Type: EXPERIMENTAL

OPB-111077

Intervention Type: DRUG

Tablet, Oral, 300mg/500mg/700mg/900mg 4 days-on \& 3 days-off (21 days=1cycle)

Interventions

OPB-111077

Tablet, Oral, 300mg/500mg/700mg/900mg 4 days-on \& 3 days-off (21 days=1cycle)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Pathologically and/or cytologically confirmed advanced solid tumor

2. Patients who were refractory to standard therapy or for which there are no standard treatment options available

3. Age 20 to 80 years at the time of informed consent

4. Patients who, together with their partner, are willing and capable of using an appropriate method of contraception throughout the trial period and until at least 12 weeks after final IMP administration

5. Patients informed of the diagnosis of advanced solid tumor who are fully informed about the content of the study by the investigator or subinvestigator using the specified written consent form and other written explanation, and give written consent to participate in the study of their free will

6. Patients who are able to take oral medication

3. Patients with active infections needing whole body therapy

4. Patients with positive hepatitis B surface (HBs) antigen or positive hepatitis C virus (HCV) antibody

5. Patients with positive human immunodeficiency virus (HIV) antibody

6. Patients with uncontrollable cardiac diseases

7. Patients with uncontrollable pain by analgesic drugs

8. Patients with a history of organ transplantation

9. Patients who have received another IMP

10. Patients who are pregnant, possibly pregnant, or lactating

11. Patients otherwise judged by the investigator or subinvestigator to be inappropriate for inclusion in the trial

Exclusion Criteria

1. Patients with symptomatic brain metastases

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Otsuka Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: collaborator

Korea Otsuka Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Doyoun Oh, MD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Hospital

Jeehyun Kim, MD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Bundang Hospital

Sungbae Kim, MD

Role: PRINCIPAL_INVESTIGATOR

Asan Medical Center

Locations

Asan Medical Center

Seoul, , South Korea

Seoul National University Bundang Hospital

Seoul, , South Korea

Seoul National University Hospital

Seoul, , South Korea

Countries

South Korea

Other Identifiers

317-KOA-1401i

Identifier Type: -

Identifier Source: org_study_id