Study of ENMD-2076 in Patients With Advanced/Metastatic Soft Tissue Sarcoma

Soft Tissue Sarcoma Clinical Trial

Official title:

A Phase II Study of Oral ENMD-2076 Administered to Patients With Advanced/Metastatic Soft Tissue Sarcoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01719744
• Other study ID #: 2076-STS-001
• Status: Completed
• Phase: Phase 2
• Start date: January 2013
• Est. completion date: January 2016

Study information

• Verified date: July 2023
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 2 study of ENMD-2076 in patients with advanced/metastatic soft tissue sarcoma. This study will help to understand how well ENMD-2076 works and how safe and tolerable the drug is in this patient population.

Description:

ENMD-2076 is an oral drug that works by blocking certain enzymes called Aurora A from working. These enzymes are needed for cells to divide including cancer cells. ENMD-2076 also works by stopping the growth of new blood vessels which would provide the tumor with nutrients for it to grow. It is believed that by blocking Aurora A enzymes from working and stopping new blood vessels from growing, the tumors may stop growing or shrink.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: January 2016
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Have documented histological diagnosis of soft tissue sarcoma (e.g. leiomyosarcoma, synovial sarcoma, angiosarcoma and liposarcoma etc), with the exception of gastrointestinal stromal tumor (GIST).

• Meet revised RECIST criteria (version 1.1) within 4 weeks of entry by having measurable disease defined as one or more lesions that can be accurately measured in one or more dimensions. Areas of previous radiation may not serve as measurable disease unless there has been objective interval tumor growth documented radiologically.

• Must have had no more than 1 line of treatment in the advanced/metastatic setting. The use of prior anti-angiogenic therapy is allowed. Previous neo-adjuvant or adjuvant therapies are allowed.

• Are at least 3 weeks from major surgery or radiation therapy and recovered; 3 weeks from any other previous anticancer therapy and recovered including biologics.

• Are = 18 years of age

• The patient has a multigated acquisition (MUGA) scan with an actual left ventricular ejection fraction of greater than or equal to the institution lower limit of normal within one month prior to start of study.

• Have clinically acceptable laboratory screening results within certain limits specified below:

• AST and ALT = 2.5 times upper limit of normal (ULN) or less than or equal to 5 times ULN if liver metastases are present

• Total bilirubin = 1.5 x ULN

• Creatinine = 1.5 x ULN or > 50 ml/min calculated by the Cockcroft and Gault formula (formula defined in appendix E).

• Absolute neutrophil count = 1500 cells/mm3

• Platelets = 100,000/mm3

• Hemoglobin = 9.0 g/dL

• INR = 1.5

• Have an ECOG performance status of 0 or 1.

• Patients must have and consent for access to archival material (for correlative studies). Patients who do not have archival material will be eligible if they consent for fresh tissue biopsy.

• Women of child producing potential must agree to use effective contraceptive methods prior to study entry, during study participation, and for at least 30 days after the last administration of study medication. A serum pregnancy test within 72 hours prior to the initiation of therapy will be required for women of childbearing potential.

• Have the ability to understand the requirements of the study, provide written informed consent which includes authorization for release of protected health information, abide by the study restrictions, and agree to return for the required assessments.

• Able to tolerate oral medications.

Exclusion Criteria:

• Women who are pregnant or nursing

• Have active, acute, or chronic clinically significant infections or bleeding.

• Have uncontrolled hypertension (systolic blood pressure greater than 150mmHg or diastolic blood pressure greater than 100mmHg); or history of congestive heart failure (equal to or greater than Grade 2 classification by New York Heath Association).

• Have active angina pectoris, stroke or recent myocardial infarction (within 6 months).

• Have chronic atrial fibrillation or QTc interval corrected for heart rate of greater than 480 msec.

• Have additional uncontrolled serious medical or psychiatric illness.

• Require therapeutic doses of anti-coagulation either by virtue of low-molecular weight heparin or coumadin (prophylactic anti-coagulation allowed). Patients with previous history of deep venous thrombosis or pulmonary embolism are also excluded.

• Known CNS metastases

• Have any medical condition that would impair the administration of oral agents including recurrent bowel obstructions, inflammatory bowel disease or uncontrolled nausea, vomiting or diarrhea

• Have 2+ protein by urinalysis. Patients with an ongoing or previous history of nephrotic syndrome will be excluded

• Have an additional malignancy diagnosed within 5 years of study enrollment with the exception of basal or squamous cell skin cancer or cervical cancer in situ

• Require treatment with drugs known to be potent inducers or inhibitors of CYP3A4 that cannot be substituted

• Patients who cannot or refuse to stop herbal medications of illicit drug use will be excluded from the study. Use of medical marijuana is not permissible in this study.

Related Conditions & MeSH terms

• Advanced
• Metastatic
• Sarcoma
• Soft Tissue Sarcoma

Intervention

Drug:
• ENMD-2076

Locations

Country	Name	City	State
Canada	Princess Margaret Cancer Centre	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	6-month Progression-free Survival Rate (PFS)	Number of patients with no progression of disease at 6 months	From start of study treatment until disease progression or death, whichever occurs first, up to 6 months.
Secondary	Number of and Severity of Adverse Events Per Participant	Number of participants who experienced a grade 3 or higher adverse event. Reporting threshold 5%	2 years
Secondary	Objective Response Rate	Objective Response Rate (ORR) = CR+ PR. ORR is evaluated per RECIST v1.1 criteria.; Complete Response (CR): Disappearance of all target lesions; Partial Response (PR): At least a 30% decrease in the sum of diameters of target lesions.	From start of study treatment until disease progression or death, whichever occurs first.