MEDI-573 in Combination With SOC in Unresectable or Metastatic HCC.

MedImmune LLC6 enrolled

Overview

A Phase 1b/2, open-label, randomized study to evaluate MEDI-573 in combination with standard of care in adult subjects with unresectable or metastatic hepatocellular carcinoma (HCC).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Unresectable or Metastatic Hepatocellular Carcinoma (HCC)

Interventions

MEDI-573 (1 of 3 doses)DRUG

MEDI-573, a human immunoglobulin G2 lambda (IgG2λ) monoclonal antibody (MAb), is a dual-targeting human antibody that neutralizes insulin-like growth factor (IGF)-I and IGF-II ligands

SorafenibDRUG

Sorafenib is a tyrosine kinase inhibitor, anti-angiogenic, VEGF inhibitor

Eligibility

Sex: ALLMin age: 18 YearsMax age: 99 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age ≥ 18 years or minimum age of consent per local regulations at the time of screening * Unresectable or metastatic hepatocellular carcinoma * ECOG Performance Status ≤ 2 * Life expectancy of ≥ 3 months; Exclusion Criteria: * Child-Pugh Score for Cirrhosis Mortality \> 7 points * Prior or current system anti-cancer therapy for HCC, including cytotoxic, biologic, targeted or experimental therapy * Prior local treatment for HCC less than 4 weeks prior to initiating study treatment * Active second malignancy * Major surgery, open biopsy or significant traumatic injury within 4 weeks prior to initiating study treatment * Thrombotic or embolic events within 6 months prior to initiating study treatment * Ongoing pancreatitis * Uncontrolled or refractory ascites * Evidence of ongoing spinal cord compression, known carcinomatous meningitis, or known leptomeningeal carcinomatosis * Hepatic encephalopathy \> Grade 1 * Active brain metastases with exceptions * Poorly controlled diabetes mellitus * Active coronary artery disease * Uncontrolled hypertension

Locations (3)

Research Site

Oxnard, California, United States

Research Site

Golden Springs, Colorado, United States

Research Site

Las Vegas, Nevada, United States

Outcomes

Primary Outcomes

Phase 1b: Number of Participants With Dose-limiting Toxicities (DLTs)

The DLT was defined as any Grade 3 or higher hematologic or non-hematologic toxicity considered to be related to MEDI-573 that occurred during the DLT evaluation period (Days 1 to 21 of Cycle 1), with the exceptions of Grade 3 fever (occurred in the absence of neutropenia and resolved to normal or baseline within 24 hours of treatment and was not considered as SAE), Grade 3 rigors/chills that responded to optimal therapy, and Grade \< 4 hyperglycemia that resolved in \< 24 hours.

Time frame: Day 1 to Day 21 of Cycle 1

Phase 1b: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Events (SAEs)

An Adverse Event (AE) is any unfavourable and unintended sign, symptoms, or diseases temporally associated with use of study drug, whether or not considered related to study drug. A serious adverse event (SAE) is an AE that results in death, initial or prolonged inpatient hospitalization, life-threatening, persistent or significant disability/incapacity, congenital anomaly/birth defect, or an important medical event. The TEAEs are defined as AEs present at baseline that worsened in intensity after administration of study drug, or events absent at baseline that emerged after administration of study drug, up to 60 days after the last study drug or until the participants started another anticancer therapy, whichever occurred first (approximately 15 months).

Time frame: From the start of study treatment (Day 1) through 60 days after the last dose of MEDI-573 or initiation of another anticancer therapy, whichever occurred first (approximately 15 months)

Phase 1b: Number of Participants With Clinical Laboratory Abnormalities Reported as TEAEs

An abnormal laboratory finding which required an action or intervention by the investigator, or a finding judged by the investigator to represent a change beyond the range of normal physiologic fluctuation were reported as AEs. The TEAEs are defined as AEs present at baseline that worsened in intensity after administration of study drug, or events absent at baseline that emerged after administration of study drug, up to 60 days after the last study drug or until the participants started another anticancer therapy, whichever occurred first (approximately 15 months).

Data from ClinicalTrials.gov

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Secondary Outcomes

Phase 1b and Phase 2: Number of Participants With Positive Anti-drug Antibodies (ADA) to MEDI-573

Participants with positive ADA to MEDI-573 are reported in the below table. This outcome was not evaluated for Phase 2 as it was not launched by the sponsor due to strategic business reasons.

Time frame: Predose on Day 1 of every treatment cycle; end of treatment; Days 30, 60 and 90 post treatment; every 3 months post treatrment till end of study (approximately 15 months)

Phase 2: Best Overall Tumor Response

Phase 2 part of the study was not launched by the sponsor due to strategic business reasons. Therefore, this outcome was not evaluated.

Time frame: From Day 1 until disease progression or death due to any cause, whichever occurred first (approximately 15 months)

Phase 2: Objective Response Rate

Phase 2 part of the study was not launched by the sponsor due to strategic business reasons. Therefore, this outcome was not evaluated.

Time frame: From Day 1 until disease progression or death due to any cause, whichever occurred first (approximately 15 months)

Phase 2: Progression-free Survival (PFS)

Phase 2 part of the study was not launched by the sponsor due to strategic business reasons. Therefore, this outcome was not evaluated.

Time frame: From Day 1 until disease progression or death due to any cause, whichever occurred first (approximately 15 months)

Phase 2: Change in Tumor Size

Phase 2 part the study was not launched by the sponsor due to strategic business reasons. Therefore, this outcome was not evaluated.

Time frame: From Day 1 until disease progression or death due to any cause, whichever occurred first (approximately 15 months)

Phase 1b and Phase 2: Time to Reach Maximum Observed Serum Concentration (Tmax) of MEDI-573 for Cycle 1

The tmax is defined as actual sampling time to reach maximum observed serum concentration of the study drug. This outcome was not evaluated for Phase 2 as it was not launched by the sponsor due to strategic business reasons.

Time frame: Cycle 1 (pre-dose; and 5 minutes, 24 hours, Day 8, and Day 15 post-dose); and Cycle 2 Day 1 (pre-dose)

Phase 1b and Phase 2: Maximum Observed Serum Concentration (Cmax) of MEDI-573 for Cycle 1

The Cmax is the maximum observed serum concentration of study drug. This outcome was not evaluated for Phase 2 as it was not launched by the sponsor due to strategic business reasons.

Time frame: Cycle 1 (pre-dose; and 5 minutes, 24 hours, Day 8, and Day 15 post-dose); and Cycle 2 Day 1 (pre-dose)

Phase 1b and Phase 2: Area Under Serum Concentration-time Curve From Time Zero to Day 22 (AUC0-Day22) of MEDI-573 for Cycle 1

Area under the concentration-time curve from time zero to Day 22 is reported. This outcome was not evaluated for Phase 2 as it was not launched by the sponsor due to strategic business reasons.

Time frame: Cycle 1 (pre-dose; and 5 minutes, 24 hours, Day 8, and Day 15 post-dose); and Cycle 2 Day 1 (pre-dose)