A Safety Study of EPC2407, A Anti-Cancer Drug With Vascular Disrupting Activity: In Patients With Advanced Cancer

Completed · Phase 1

Conditions studied: Advanced Cancer

In brief

This study will evaluate the safety, pharmacokinetics (PK), and pharmacodynamic effects of a novel anti-cancer drug, EPC2407, administered to patients with advanced cancer which have not responded to or have recurred following treatment with available therapies

Key facts

Study ID: NCT00423410
Run by: EpiCept Corporation
People needed: 30
Starts: 2006-12-01
Expected to finish: 2009-09-01
Last updated by the study team: 2009-09-10

Who can join

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

You may qualify if…

Histologically or cytologically confirmed solid tumor or lymphoma,which has progressed on standard therapies, for which effective therapy is not available or for patients who are unwilling to undergo such therapies.
Males and Females at least 18 years of age
Laboratory data as specified below (according to the site's clinical laboratory ranges for normal):
i. Hematology: ANC >1500 cells/mm3, platelet count >100,000 cells/mm3 and Hemoglobin > 9 gm/L ii. Hepatic: Direct bilirubin <1.5 X ULN; alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 2.5 X ULN. For patients with known liver metastases or liver neoplasms: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 5.0 X ULN iii. Renal: serum creatinine WNL or creatinine clearance >60 mL/min
12-lead electrocardiogram (ECG) QT intervals: QTc ≤ 450 msec for men and ≤ 470 msec for women.
Estimated life expectancy of at least 3 months
ECOG Performance Status < or = 1
Previously treated CNS disease allowed if treatment completed and stable for 4 weeks.
For men and women of child-producing potential - willingness to employ appropriate contraceptive methods (including abstinence) during the study
Ability to understand the requirements of the study, provide written informed consent and authorization of use and disclosure of protected health information, and agree to abide by the study restrictions and to return for the required assessments
Cardiac ejection fraction ≥50% by 2D Echocardiogram or > institutional lower limits of normal

You may not qualify if…

Women who are pregnant or nursing
Radiotherapy or any chemotherapy within the previous 21 days or five half lives of prior drug (whichever is shorter). See also exclusion #4 below for patients at risk for cardiac toxicity. Recovery to Grade 1 or less from chemotherapy-induced toxic effect, except alopecia, is required.
Major surgery within the last 4 weeks or minor surgery within the last 2 weeks
Significant risk of cardiac drug toxicity due to any of the following: a) Active New York Heart Association Class III or IV, b) history of or current congestive heart failure, c) history of myocardial infarction within the last 6 months or ongoing unstable angina, or anthracycline exposure per exclusion #5.
Anthracycline exposure exceeding a cumulative dose of 360 mg/m²
Known and ongoing HIV, Hepatitis B or Hepatitis C infection
Concomitant use of strong inhibitors of the liver microsomal enzymes CYP2C8, CYP2C9, CYP2C19 and CYP3A4.
Participation in concurrent study of an investigational agent or device
Any other condition including but not limited to major co-morbidities, which in the opinion of the investigator would render the patient ineligible
O2 Saturation by pulse oximetry at rest < 90%
Concomitant use of drugs that have significant risk of Torsades de Pointes will also be prohibited. Please refer to drugs listed under "Drugs with Risk of Torsades de Pointes"

Where it is running

Scottsdale Healthcare — Scottsdale, Arizona, United States
Tower Oncology Research — Beverly Hills, California, United States
Rebecca and John Moores UCSD Cancer Center — San Diego, California, United States

Full record on ClinicalTrials.gov

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