A Safety and Efficacy Study of CC-122 in Combination With Nivolumab in Subjects With Unresectable Hepatocellular Carcinoma (HCC)

NCT ID: NCT02859324

Last Updated: 2021-05-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 21 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-09-20
• Study Completion Date: 2020-03-27

Brief Summary

CC-122-HCC-002 is a Phase 1/2 dose escalation and expansion clinical study of CC-122 in combination with nivolumab in subjects with unresectable hepatocellular carcinoma (HCC) who have progressed after or were intolerant to no more than 2 previous systemic therapies for unresectable HCC, or are naïve to systemic therapy.

Detailed Description

Study population included subjects who had progressed after or were intolerant to no more than 2 previous systemic therapies for unresectable HCC, or are naïve to systemic therapy.

The dose escalation part of the study was designed to explore three dose levels of CC-122 to identify the recommended phase 2 dose (RP2D) to be used in the expansion phase. Approximately 20 subjects were to be enrolled in the dose escalation part of the study. Subjects could be treated for up to 2 years, or until progression of disease, unacceptable toxicity, subject/physician decision, withdrawal of consent, death. Safety follow up until 28 days after CC122 treatment and 90 days after nivolumab treatment. RECIST 1.1 criteria was used to determine response. Survival follow up until death, withdrawal of consent, or the study closes. Subjects were permitted to continue treatment beyond progression (TBP) if they continue to meet protocol criteria, had stable performance status, had clinical benefit, other treatment options were discussed. A separate ICF was signed to continue TBP.

During the dose escalation phase, CC-122 was administered orally 5 consecutive days out of 7 (5 days on/2 days off weekly) on Days 1 to 5, 8 to 12, 15 to 19 and 22 to 26 of each 28-day cycle. Once the RP2D for dosing of CC-122 in combination with nivolumab was defined, expansion (Phase 2) would start. A modified 3+3 dose escalation design was used to identify the initial toxicity of the combination. Up to six subjects were concurrently enrolled into a dose level. Decisions as to which dose level to enroll a new subject were based on the number of subjects enrolled and evaluable, the number of subjects experiencing DLTs, and the number of subjects enrolled but who are not yet evaluable for toxicity in the current cohort at the time of new subject entry. A Safety Review Committee (SRC) comprised of investigators participating in the study made dose escalation decisions based on these criteria.

After completion of the Dose Escalation Phase, the Dose Expansion Phase of the study did not proceed due to the changing landscape in the treatment of HCC. There were no additional safety concerns or safety signals identified in the dose escalation phase of the study.

Conditions

Carcinoma, Hepatocellular

Study Design

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

Study Groups

CC-122 with Nivolumab

CC-122 orally 5/7 days with nivolumab Intravenously (IV) 3mg/kg every 2 weeks. Cohorts of up to 6 subjects per dose level until Recommended Phase 2 dose (RP2D).

Group Type: EXPERIMENTAL

CC-122

Intervention Type: DRUG

Nivolumab

Intervention Type: DRUG

Interventions

CC-122

Intervention Type: DRUG

Nivolumab

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subjects must satisfy the following criteria to be enrolled in the study:
• Subject is ≥ 18 years of age at the time of signing the informed consent form (ICF)
• Subject has a confirmed pathologic diagnosis of Hepatocellular carcinoma (HCC) according to the American Association for the Study of Liver Diseases (AASLD) Guidelines.
• Subjects who have progressed after or were intolerant to no more than 2 previous systemic therapies for unresectable HCC, or are naïve to systemic therapy.
• Subject has at least one measurable lesion according to RECIST 1.1.
• Subject has a life expectancy of ≥ 12 weeks
• Subject has an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1
• Subject has adequate hematologic function and adequate hepatic function at screening

Exclusion Criteria

• The presence of any of the following will exclude a subject from enrollment:
• Subject has received more than 2 previous systemic therapies for Hepatocellular carcinoma (HCC).
• Subject has received previous treatment with any anti-PD-1 (Programmed death 1) or anti-PD-L1 (PD-1 ligand receptor) antibody

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Celgene

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Akshay Patel

Role: STUDY_DIRECTOR

Celgene Corporation

Locations

UCLA Division of Hematology Oncology

Los Angeles, California, United States

University of Florida

Gainesville, Florida, United States

NYU Langone Medical Center

New York, New York, United States

Mary Crowley Cancer Research

Dallas, Texas, United States

Institut Paoli Calmettes

Marseille, , France

Centre Eugene Marquis

Rennes, , France

Institut Universitaire du Cancer IUCT - Oncopole

Toulouse, , France

Institut Gustave Roussy Hematologie

Villejuif, , France

IRCCS - Istituo Clinico Humanitas - Humanitas Cancer Center

Milan, , Italy

Fondazione IRCCS Policlinico San Matteo

Pavia, , Italy

Istituto Nazionale Tumori Regina Elena

Roma, , Italy

Hospital Universitario Vall D Hebron

Barcelona, , Spain

Hospital Ramon y Cajal

Madrid, , Spain

Hospital 12 de Octubre

Madrid, , Spain

Countries

United States; France; Italy; Spain

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

2016-000112-15

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CC-122-HCC-002

Identifier Type: -

Identifier Source: org_study_id