A Phase I, Open-label, Ascending Dose Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of the Endothelin B Agonist, SPI-1620, in Patients With Recurrent or Progressive Carcinoma

Completed · Phase 1

Conditions studied: Carcinoma

In brief

This is a 2-part, open-label, single-arm, dose escalation study. Part I will define the Maximum Tolerated Dose (MTD) and optimal dose of SPI-1620 and evaluate its PK and PD properties. Once the MTD for SPI-1620 is identified, a second phase of the study will focus on dose escalation of docetaxel studied in groups of 3-6 patients. This part of the study will assess the safety and tolerability of increasing doses of docetaxel administered with the optimal dose of SPI 1620 defined in Part I.

Key facts

Study ID

NCT00613691

Run by

Spectrum Pharmaceuticals, Inc

People needed

36

Starts

2008-01-01

Expected to finish

2012-12-01

Last updated by the study team

2013-10-21

Who can join

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

You may qualify if…

• All of the following inclusion criteria must be met prior to participation in this study
• The patient must sign an informed consent. A signed consent form is required prior to the performance of any protocol-related procedures or assessments.
• The patient must be >= 18 years of age.
• The patient must have progressive or recurrent carcinoma and has failed all standard therapies for his/her tumor.
• The patient must have a negative CT scan with contrast of the brain or MRI of the brain within 45 days of enrollment.
• The patient must be using an acceptable/effective method of contraception if she is a female patient of childbearing potential.
• The patient must have a negative serum pregnancy test within 14 days of entering the protocol if she is a female of childbearing potential.
• The patient must have an ECOG score <= 2.
• The patient must be willing and able to abide by the protocol.

You may not qualify if…

• None of the exclusion criteria may be met prior to patient participation in this study
• The patient has a history of CHF, migraines, coagulopathy, stroke or inadequately controlled hypertension.
• The patient has asthma or symptomatic COPD.
• The patient has autonomic nerve dysregulation syndrome.
• The patient has angina or is taking nitrates or has had a MI within the past six months.
• The patient has a significant ventricular arrhythmia, class III or IV CHF or has a known coronary stenoses >80% and has not undergone either angioplasty or CABG
• The patient is taking phosphodiesterase inhibitors
• The patient has malignant or poorly controlled hypertension (>160/100)
• The patient has symptomatic orthostatic hypotension
• The patient is taking arterial vasodilators such as nifedipine or amlodipine or alpha blockers such as terazosin, tamsulosin and prazosin.
• The patient has a screening absolute neutrophil count less than 1.5 K/uL
• The patient has a screening platelet count less than 100 K/uL.
• The patient has a screening creatinine greater than 2.0 mg/dL
• The patient has a screening amino alanine transferase (ALT), or aspartate aminotransferase (AST) > 2.5 times the upper limit of the laboratory reference range or a total bilirubin > 1.0 mg/dL.
• The patient has a known immunodeficiency disorder.
• The patient is enrolled, or the patient plans to enroll, in any concurrent study of another investigational product.
• The patient is taking, or the patient is planning to take other cancer treatments during the study except for patients with prostate cancer using LHRH agonist therapy.
• The patient has a known hypersensitivity to any of the components of SPI 1620 or to docetaxel.
• The patient has previously failed treatment with docetaxel for his/her tumor and a dose of SPI-1620 that has been shown to enhance tumor blood flow has not been identified.
• The patient does not have a tumor that is at least 1cm. -

Where it is running

• START — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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