A Study of ARRY-380 in Patients With Advanced HER2+ Cancer

NCT00650572 | Completed Phase 1

• 1 other identifier: ARRAY-380-101
• Study Type: interventional
• Target: 50
• Locations: 2 countries
• Sites: 4

Brief Summary

This is a Phase 1 study during which patients with advanced HER2+ solid malignancies or HER2+ metastatic breast cancer will receive investigational study drug ARRY-380. This study has 2 parts. In the first part, patients with advanced HER2+ solid malignancies, who have already received at least one previous standard therapy, will receive increasing doses of study drug in order to achieve the highest dose of study drug possible that will not cause unacceptable side effects. Approximately 30 patients from the US will be enrolled in Part 1 (Completed). In the second part of this study, patients with HER2+ metastatic breast cancer, who have already received at least one previous standard therapy, will receive the best dose of study drug determined from the first part of the study and will be followed to see what side effects and effectiveness the study drug has, if any, in treating the cancer. Approximately 20 patients from the US will be enrolled in Part 2 (Active, not recruiting).

Conditions

Cancer

Keywords

human epidermal growth factor receptor 2; epidermal growth factor receptor; EGFR; type I receptor tyrosine kinase

Outcome Measures

Primary Outcomes (4)

• Characterize the safety profile of the study drug in terms of adverse events, clinical laboratory tests and electrocardiograms.

  Part 1, one year; Part 2, one year

• Establish the maximum tolerated dose (MTD) of the study drug.

  Part 1, one year

• Characterize the pharmacokinetics of the study drug.

  Part 2, one year

• Assess amplification/expression of HER2 in archival and tumor tissues.

  Part 2, one year

Secondary Outcomes (4)

• Characterize the pharmacokinetics of the study drug.

  Part 1, one year

• Assess changes in tumor markers.

  Part 1, one year

• Assess the efficacy of study drug in terms of tumor response and duration of response.

  Part 1, one year; Part 2, one year

• Assess expression of growth factor pathway proteins in archival and tumor tissues.

  Part 2, one year

Study Arms (1)

ARRY-380

EXPERIMENTAL

Drug: ARRY-380, HER2 inhibitor; oral

Interventions

ARRY-380, HER2 inhibitor; oral DRUG

Part 1: multiple dose, escalating; Part 2: multiple dose, single schedule.

ARRY-380

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Histological or cytological evidence of HER2+ cancer (Part 1) or HER2+ metastatic breast cancer (Part 2).
• Patients should have received at least one previous therapeutic regimen and either no longer are candidates for standard therapy, have no standard therapy available, or choose not to pursue standard therapy (patients with HER2+ breast cancer and with clinical indication for trastuzumab or lapatinib should have received prior therapy with trastuzumab and lapatinib, if available).
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) between 0 and 2.
• Additional criteria exist.

You may not qualify if:

• Uncontrolled or symptomatic brain metastases (patients may be considered adequately controlled if on a stable steroid dose for at least 30 days).
• Treatment with an investigational medicinal product or device within 30 days prior to first dose of study drug.
• Radiotherapy within 28 days prior to first dose of study drug (not including palliative radiotherapy at focal sites).
• Chemotherapy within 21 days prior to first dose of study drug.
• Major surgery within 30 days prior to first dose of study drug.
• Known positive serology for the human immunodeficiency virus (HIV), hepatitis B and/or active hepatitis C.
• Additional criteria exist.

Sponsors & Collaborators

• Seagen Inc.: lead
• Array BioPharma: collaborator

Study Sites (4)

The University of Colorado Cancer Center

Aurora, Colorado, United States

Location

The University of Texas, MD Anderson Cancer Center

Houston, Texas, 77230, United States

Location

British Columbia Cancer Agency

Vancouver, British Columbia, V5Z 4E6, Canada

Location

Cancer Centre of Southeastern Ontario at Kingston General Hospital

Kingston, Ontario, K7L 5P9, Canada

Location

MeSH Terms

Conditions

Neoplasms

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 31, 2008
• First Posted: April 2, 2008
• Study Start: May 1, 2008
• Primary Completion: March 1, 2013
• Study Completion: March 1, 2013
• Last Updated: May 7, 2020

Record last verified: 2020-05

Locations

US (2); CA (2)