A Study of Dulanermin Administered in Combination With Camptosar®/Erbitux® Chemotherapy or FOLFIRI (With or Without Bevacizumab) in Subjects With Previously Treated Metastatic Colorectal Cancer

A Phase Ib, Open-Label, Dose-Escalation Study of the Safety and Pharmacokinetics of Multiple Doses of Dulanermin Administered Intravenously in Combination With Camptosar®/Erbitux® Chemotherapy or the Folfiri Regimen With or Without Bevacizumab in Subjects With Previously Treated Metastatic Colorectal Cancer

This study will assess the safety and pharmacokinetics of adding dulanermin to Camptosar®/Erbitux® or the FOLFIRI regimen (Camptosar®, 5-FU, and leucovorin) plus bevacizumab (only for Cohort 6 subjects who have not received prior bevacizumab therapy).

Study Overview

• Status: Completed
• Conditions: Colorectal Cancer
• Intervention / Treatment: Drug: irinotecan; Drug: dulanermin; Drug: cetuximab; Drug: FOLFIRI regimen; Drug: bevacizumab

• Study Type: Interventional
• Enrollment (Actual): 42
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • California
    • Los Angeles, California, United States, 90095
    • Redlands, California, United States, 92374
    • San Francisco, California, United States, 94115
  • Florida
    • Fort Myers, Florida, United States, 33916
  • Illinois
    • Harvey, Illinois, United States, 60426
  • New York
    • Buffalo, New York, United States, 14263
  • North Carolina
    • Durham, North Carolina, United States, 27710
  • Pennsylvania
    • Hershey, Pennsylvania, United States, 17033
  • Tennessee
    • Nashville, Tennessee, United States, 37203
  • Washington
    • Tacoma, Washington, United States, 98405

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Signed Informed Consent Form
• Age >= 18 years
• Histologically confirmed CRC with evidence of metastases and measurable tumor lesion(s)
• Progression of disease following, or intolerance to, treatment with 5-fluorouracil-based therapy
• Progression of disease during or within =< 6 months following the last dose of a prior first-line treatment with a fluoropyrimidine and oxaliplatin-based chemotherapy plus bevacizumab for metastatic disease
• Use of an effective means of contraception for women of childbearing potential and men with partners of childbearing potential (use per institutional standard)
• Life expectancy of > 3 months
• Willingness and capability to be accessible for study follow-up

Exclusion Criteria:

• Prior radiotherapy to a measurable, metastatic lesion(s) to be used to measure response
• Radiation therapy to a peripheral lesion within 14 days prior to Day 1; Radiation therapy to a thoracic, abdominal or pelvic field within 28 days prior to Day 1
• Chemotherapy, hormonal therapy, or immunology within 4 weeks prior to Day 1
• Previous exposure to DR4-targeted therapy or DR5-targeted therapy
• Evidence of clinically detectable ascites on Day
• Other invasive malignancies within 5 years prior to Day 1 (other than basal cell carcinoma of the skin or in situ carcinoma of the cervix)
• History or evidence upon physical examination of CNS disease
• Active infection requiring parenteral antibiotics on Day 1
• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1 or anticipation of need for major surgical procedure during the course of the study and fine needle aspirations within 7 days prior to Day 1
• Pregnancy or lactation
• Serious nonhealing wound, ulcer, or bone fracture
• Current or recent participation in another experimental drug study
• Clinically significant cardiovascular disease
• History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates use of an investigational drug or that might affect interpretation of the results of the study or render the subject at high risk from treatment complications
• Cohort 5 only: Subjects who have a Kras mutation will be excluded from enrollment
• The following exclusion criteria apply only to subjects who have received prior bevacizumab and are enrolled in Cohort 6: four or more prior doses of bevacizumab therapy, inadequately controlled hypertension, history of hypertensive crisis or hypertensive encephalopathy, history of arterial thromboembolic event 6 months prior to Day 1, proteinuria, history of abdominal fistula or gastrointestinal perforation within 6 months prior to Day 1

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Cohorts 1-5	Drug: irinotecan; Intravenous repeating dose; Drug: dulanermin; Intravenous repeating dose; Drug: cetuximab; Intravenous repeating dose
EXPERIMENTAL: Cohorts 6, 6A, 7, 7A	Drug: dulanermin; Intravenous repeating dose; Drug: FOLFIRI regimen; Intravenous repeating dose; Drug: bevacizumab; Intravenous repeating dose (for Cohort 6 subjects not previously treated with bevacizumab)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
The safety and tolerability of dulanermin administered in combination with Camptosar and Erbitux	Length of study
The safety and tolerability of dulanermin administered in combination with FOLFIRI (with or without Bevacizumab)	Length of study

Collaborators and Investigators

• Sponsor: Genentech, Inc.

Study record dates

Study Major Dates

• Study Start: July 1, 2006
• Primary Completion (ACTUAL): March 1, 2012
• Study Completion (ACTUAL): March 1, 2012

Study Registration Dates

• First Submitted: April 18, 2008
• First Submitted That Met QC Criteria: April 30, 2008
• First Posted (ESTIMATE): May 5, 2008

Study Record Updates

• Last Update Posted (ESTIMATE): November 2, 2016
• Last Update Submitted That Met QC Criteria: November 1, 2016
• Last Verified: November 1, 2016

More Information

Terms related to this study

• Keywords: CRC; Metastatic CRC; APO2L/TRAIL
• Additional Relevant MeSH Terms: Digestive System Diseases; Neoplasms; Neoplasms by Site; Gastrointestinal Neoplasms; Digestive System Neoplasms; Gastrointestinal Diseases; Colonic Diseases; Intestinal Diseases; Intestinal Neoplasms; Rectal Diseases; Colorectal Neoplasms; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antineoplastic Agents; Topoisomerase Inhibitors; Antineoplastic Agents, Immunological; Angiogenesis Inhibitors; Angiogenesis Modulating Agents; Growth Substances; Growth Inhibitors; Topoisomerase I Inhibitors; Bevacizumab; Irinotecan; Cetuximab
• Other Study ID Numbers: APO3583g; GO00933