A Safety, Pharmacokinetic and Pharmacodynamic Study of Kevetrin in Patients With Advanced Solid Tumors

Cellceutix

Status and phase

Completed

Phase 1

Conditions

Solid Tumors

Treatments

Drug: thioureidobutyronitrile

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01664000

12-151 (Other Identifier)

CTIX 12-101

Details and patient eligibility

About

In the laboratory, Kevetrin activates p53, a tumor suppressor protein that has an important role in protecting the body. p53 functions by activating proteins that repair DNA and kill cells that have genetic mutations such as in cancers. Research experiments showed that when cancer cells were treated with Kevetrin, it activated p53 which induced p21, a protein that inhibits cancer cell growth. p53 also induced PUMA (p53 up-regulated modulator of apoptosis), a protein that causes tumor cell death. Because of these activities, slowing cancer cell growth and causing cancer cell death, Kevetrin may help to treat tumors.

Full description

Kevetrin was found to be effective in pre-clinical studies of human xenograft tumor models and was reasonably well-tolerated at therapeutic doses in the non-clinical animal studies. Kevetrin was also effective in multi-drug resistant tumor models; therefore, Kevetrin has the potential to treat tumors that have become resistant to standard chemotherapy. This trial will determine tolerance in humans and, possibly, efficacy with a Phase I, open-label, dose-escalation, safety, pharmacokinetic, and pharmacodynamic study of Kevetrin, in adult patients with solid tumors.

The primary objectives are the following:

To determine the maximum tolerated dose (MTD) of Kevetrin.
To determine the dose limiting toxicities (DLT) of Kevetrin.
To establish a safe dose level of Kevetrin that can be used for future studies.

The secondary objectives are to determine the following:

The pharmacokinetics of Kevetrin in humans.
Observe for evidence of antitumor activity following administration of Kevetrin.
If Kevetrin induces changes in the biomarker p21 in peripheral blood lymphocytes.
If there is a pharmacodynamic relationship between the plasma concentrations of Kevetrin and a clinical or cellular effect.

During each 4 week cycle, each patient will receive three weekly doses of Kevetrin given as a 1 hour intravenous infusion followed by a 1 week off-treatment period. Following each dose, each patient will be monitored. If the patients have acceptable safety and tolerance, Kevetrin will be given once weekly for a total of 3 weeks. During each cycle patients will be evaluated for safety, tolerance, and Dose-Limiting Toxicity (DLT) that occur during a cycle.

Enrollment

48 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Males / females, ≥ 18 years old, any race / ethnicity, who can provide written Informed Consent
Life expectancy ≥ 3 months
Pathologically confirmed solid tumor, locally advanced / metastatic, refractory after standard therapy, or for which no effective curative or surgical treatment options are available
Measurable disease on baseline imaging per RECIST 1.1 criteria
ECOG performance status ≤ 1
Liver function:
Bilirubin ≤ 1.5 X upper limit of normal
AST, SGOT, ALT, SGPT ≤ 2.5 X upper limit of normal, < 5 upper limit if there are liver metastases
Renal function:
Serum creatinine within normal limits
Hematologic status:
Absolute neutrophil count ≥ 1500 cells/mm3.
Platelet count ≥ 100,000/mm3.
Hemoglobin ≥ 9 g/dL
Coagulation status:
Coagulation Prothrombin time ≤ 1.5 X upper limit
Partial thromboplastin time ≤ 1.5 X upper limit
Males must agree to use condoms during sex to prevent spillage of semen for the duration of the study and for 3 months after the patient leaves the study
Females in the study must not be pregnant or breast feeding and not planning to become pregnant or breast feed for the duration of the study, and for at least three months after study completion
Women of childbearing potential must commit to using a double barrier method of contraception, an intrauterine device, or sexual abstinence for the duration of the study and for at least three months after study completion
Serum pregnancy test for women of child bearing potential must be negative at entry into study
Written voluntary informed consent: the patient is capable of complying with the requirements of the written Informed Consent Form and complying with protocol requirements

Exclusion criteria

History of significant disease that in the Investigator's opinion would put the patient at high risk on the trial
Cognitive impairment sufficient to render the patient incapable of giving informed consent
History of clinically significant psychiatric illness that would prevent the patient from providing a valid ICF and complying with protocol requirements
Unwillingness or inability to comply with procedures required in this protocol
History or presence of alcoholism or drug abuse within the past 2 years
Patients who have had a major surgical procedure within the past 6 weeks
History of HIV, hepatitis B, or hepatitis C
Active, uncontrolled bacterial, viral, or fungal infections requiring systemic therapy
Women of childbearing potential who are lactating, pregnant or there is the likelihood of becoming pregnant within the coming 12 months; a positive serum beta-human chorionic gonadotropin test at time of screening for entry into study
New York Heart Association Class III or IV, cardiac disease, myocardial infarction within the past 6 months, unstable arrhythmia, or evidence of ischemia on ECG
Patients with a mean QTc interval greater than 480ms are excluded. Avoid concomitant administration of agents that prolong the QT interval, except at the discretion of the investigator. If advised, patients should discontinue the use of these agents at least 2 weeks before the study begins. No uncontrolled arrhythmias.
Patients currently receiving other investigational agents
Participation in a study of an investigational drug within 4 weeks prior to the planned first day of study drug administration
Patients who have undergone radiation within the past 4 weeks
Treatment with molecularly targeted agents within the past 3 weeks prior to planned first study drug administration. Patients who were receiving standard chemotherapy or experimental therapies must wait 4 weeks from their last dose prior to the planned first study drug administration. Patients treated with nitrosoureas or mitomycin C must wait 6 weeks from their last dose prior to the planned first study drug administration.
Patients with known brain metastases may be excluded from this study. However, patients may be eligible if scans show limited disease or repeat scans show stable disease in the opinion of the investigator and patients have no ill effect from the metastases.
Herbal supplements are prohibited 1 week prior to the planned first study drug administration, during the clinical study, and up to the time that the patient is discharged from the study
Patients who have been exposed to medications, herbal preparations, or foods known to be predominant Cytochrome P450 2C9, 2C19, 2D6, 3A4/5 substrates, strong inhibitors or inducers within 7 days of planned first study treatment day
Patients who in the opinion of the Investigator would not be able to provide reliable study data or be available for study follow-up