Phase I Dose Escalation Study of VS-4718 in Subjects With Metastatic Non-Hematologic Malignancies

Stopped early · Phase 1

Conditions studied: Non Hematologic Cancers, Metastatic Cancer

In brief

This is a Phase I, open-label, multicenter, dose-escalation trial of VS-4718, a focal adhesion kinase inhibitor, in subjects with metastatic non-hematologic malignancies. This clinical study is comprised of 2 parts: Part 1 (Dose Escalation) and Part 2 (Expansion). The purpose of this study is to evaluate the safety (including the recommended Phase II dose), pharmacokinetics (the amount of VS-4718 in your blood) and the anti-cancer activity of VS-4718. The pharmacodynamic effects (genes or proteins that may predict or show how your body may respond to VS-4718) will also be examined in tumor biopsies and blood samples.

Key facts

Study ID

NCT01849744

Run by

Verastem, Inc.

People needed

48

Starts

2013-06-01

Expected to finish

2017-06-01

Last updated by the study team

2017-07-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years.
• Histopathologically confirmed diagnosis of a metastatic non-hematologic malignancy.
• ECOG (Eastern Cooperative Oncology Group) performance status of ≤ 2
• Adequate renal function
• Adequate hepatic function (total bilirubin ≤ 1.5x ULN (upper limit of normal) for the institution; AST [aspartate transaminase] and ALT [alanine transaminase] ≤ 3x ULN, or ≤ 5x ULN if due to liver involvement by tumor).
• Adequate bone marrow function (hemoglobin ≥ 9.0 g/dL; unsupported platelets ≥ 100 x10 9 cells/L; absolute neutrophil count ≥ 1.5x10 9 cells/L
• Corrected QT interval (QTc) < 470 ms
• Subjects must have at least one tumor lesion that is suitable for repeat biopsy, and must agree to two tumor biopsies (pre- and post- treatment).
• Willing and able to participate in the trial and comply with all trial requirements.

You may not qualify if…

• Gastrointestinal (GI) condition which could interfere with the swallowing or absorption of study medication.
• Uncontrolled or severe concurrent medical condition (including uncontrolled brain metastases).
• History of upper gastrointestinal bleeding, ulceration, or perforation within 12 months.
• Known history of stroke or cerebrovascular accident within 6 months.
• Subjects being actively treated for a secondary malignancy.

Where it is running

• HonorHealth Research Institute — Scottsdale, Arizona, United States
• Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center — Los Angeles, California, United States
• Florida Cancer Specialists — Sarasota, Florida, United States
• Washington University School of Medicine, Division of Oncology — St Louis, Missouri, United States
• Sarah Cannon Research Institute — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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