Study of Intravenous TCD-717 in Patients With Advanced Solid Tumors

Advanced Solid Tumors Clinical Trial

Official title:

A Multicenter Phase I Study of TCD-717 Given by 4-Hour Intravenous Infusion in Patients With Advanced Solid Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01215864
• Other study ID #: T10-10646
• Status: Completed
• Phase: Phase 1
• First received: October 5, 2010
• Last updated: August 7, 2014
• Start date: January 2011
• Est. completion date: February 2014

Study information

• Verified date: August 2014
• Source: Traslational Cancer Drugs Pharma, SL
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a Phase I dose escalation study of TCD-717, a novel drug that is a specific inhibitor of the enzyme choline kinase alpha, in patients with advanced solid tumors. The objectives of this study are to evaluate the safety of the drug and to determine the maximum tolerated dose and appropriate dose for phase II studies. Secondary objectives are to measure the efficacy of TCD-717; and in a substudy to be conducted in the MTD confirmation cohort only, to evaluate the potential correlation between the levels of tumor choline and tumor response to the choline kinase alpha inhibitor, TCD-717, using magnetic resonance spectroscopy. Pharmacokinetics analysis will be performed on patients enrolled in the maximum tolerated dose confirmation cohort.

Description:

TCD Pharma has developed TCD-717, a novel drug that is a specific inhibitor of the enzyme choline kinase alpha (ChoKα), involved in the synthesis of phosphatidylcholine, which constitutes the major phospholipid in eukaryotic cell membranes and has been described as a potent oncogen when overexpressed in human cells. TCD-717 will be evaluated in this Phase I, open-label, single arm study to be performed at multiple centers. TCD-717 will be administered as a 4 hour infusion on two separate days per 7-day period per 28-day cycle (8 administrations per cycle). Eligible patients must have confirmed, metastatic or recurrent/refractory solid tumors.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: February 2014
• Est. primary completion date: February 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients must have histologically-confirmed solid tumors, metastatic or recurrent and refractory after standard therapy for the disease or for which conventional therapy is not reliably effective or no effective therapy is available.

2. Where possible, it is recommended that a paraffin block of tumor tissue or slides containing sections of tumor tissue be available (a sample should be collected and stored appropriately for the potential evaluation of choline kinase alpha expression in tumor tissue at the end of the study).

3. Patients must be = 18 years of age.

4. Patients must have an ECOG Performance Status of 0, 1 or 2 and an estimated life expectancy of = 12 weeks.

5. Patients must have adequate clinical laboratory values (i.e., absolute neutrophil count =1.5x10^9/L, platelets =100x10^9/L, plasma creatinine <= 1.5 x upper limit of normal (ULN) for the institution or a calculated creatinine clearance (using Cockroft and Gault formula) of = 60 mL/min/1.73 m^2; bilirubin < 1.5 x ULN, alanine transaminase (ALT) and aspartate transaminase (AST) < 2.5 x ULN or = 5 x ULN with liver involvement.

6. Patients may have either measurable or non-measurable disease as defined by RECIST.

7. Patients must give signed informed consent prior to the start of any study specific procedures.

8. Female patients with reproductive potential must have a negative serum or urine pregnancy test.

9. Patients with reproductive potential and their partners must be using at least one form of contraception as approved by the Investigator prior to study entry.

10. Patients with central nervous system metastases may be included if they are stable without administration of steroids. Patients with unstable metastatic CNS disease are excluded.

Exclusion Criteria:

1. Patients will be excluded if they have received previous anti-cancer chemotherapy, immunotherapy, vaccines, monoclonal antibodies, anti-angiogenic therapy, radiotherapy or any other investigational therapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to study entry. Patients receiving concurrent anticancer therapy or intending to receive this at any time during the study will be excluded.

2. Patients who have received extensive prior radiotherapy to more than 30% of bone marrow reserves, or prior bone marrow/stem cell transplantation at any time prior to the study.

3. Patients with any concomitant condition that could compromise the objectives of this study and the patient's compliance.

4. Patients with significant cardiac disease including heart failure that meets New York Heart Association (NYHA) class III and IV definitions, history of myocardial infarction within six months of study entry, uncontrolled dysrhythmias or poorly controlled angina, uncontrolled hypertension or elevated heart rate.

5. Patients with a history of serious ventricular arrhythmia (VT or VF), QTc >=450 msec for men and 470 msec for women (as indicated in the ECG taken in the pre-treatment evaluation), or left ventricular ejection fraction (LVEF)<=50% by MUGA or Echocardiogram performed at the pre-treatment evaluation.

6. Pregnant or lactating females.

7. Patients with clinically evident HIV, HBV or HCV infection.

8. Patients with a hematologic malignancy.

9. Patients with a documented or known bleeding disorder or who require anticoagulation treatment that increases international normalized ratio (INR) or activated partial thromboplastin time (aPTT) above the institutional upper limit of normal.

10. Patients with clinically significant retinal abnormalities as per the medical history or ophthalmologic findings in the pre-treatment evaluation (e.g., retinitis pigmentosa or macular degeneration).

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Advanced Solid Tumors

Intervention

Drug:
• TCD-717
Patients will receive TCD-717 at the following dose levels: 2, 4, 7, 10, 14, 19, 25, 31, 39, 49 or 61 mg/m^2

Locations

Country	Name	City	State
United States	Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins	Baltimore	Maryland
United States	Barbara Ann Karmanos Cancer Institute	Detroit	Michigan

Sponsors (1)

Lead Sponsor	Collaborator
Traslational Cancer Drugs Pharma, SL

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety of TCD-717 given by 4-hour intravenous infusion	Patients will be monitored throughout the study for adverse events and dose limting toxicities.	Duration of the study	No
Secondary	Antitumor activity of TCD-717 given by 4-hour intravenous infusion	Efficacy of TCD-717 will be asessed by RECIST 1.1	Duration of study	No
Secondary	MTD confirmation cohort only: Pharmacokinetics (PK) of TCD-717 given by 4-hour infusion	For patients enrolled in MTD confirmation cohort, PK (Cmax, Tmax, AUC) will be measured during Cycle 1	Day 1-28 of Cycle 1	No
Secondary	To evaluate the potential correlation between the levels of tumor choline and tumor response to the choline kinase alpha inhibitor TCD-717 using magnetic resonance spectroscopy (MRS) (Substudy, MTD confirmation cohort only).	MTD confirmation cohort only	First scan will be pre-treatment (within 2 wks prior to start of treatment), then on Cycle 1 Day 25, and then within 7 days after determining disease progression	No