Study of Cordycepin Plus Pentostatin in Patients With Refractory TdT-Positive Leukemia

Refractory TdT-Positive Leukemia Clinical Trial

Official title:

A Phase I/II Study of Cordycepin Plus Pentostatin in Patients With Refractory TdT-Positive Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00709215
• Other study ID #: OV06-001
• Status: Recruiting
• Phase: Phase 1/Phase 2
• First received: June 30, 2008
• Last updated: January 8, 2009
• Start date: June 2008
• Est. completion date: December 2010

Study information

• Verified date: January 2009
• Source: OncoVista, Inc.
• Contact: Michael Moloney, MBA, BS
• Phone: 210.677.6000
• Email: michael.moloney[@]oncovista.com
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a two-part, open-label, Phase I/II study in subjects with relapsed or refractory TdT-positive leukemia for which no standard therapies are expected to result in durable remission.

Description:

In the first phase the Study Objectives are to:

• Define the maximally tolerated dose (MTD) and recommended dose (RD) for administration of cordycepin as a 1-hour IV infusion, administered 1 hour following administration of an IV bolus of pentostatin, in subjects with refractory TdT-positive leukemia;

• Determine plasma ADA levels prior to pentostatin infusion and at 60 and 120 minutes after administration of pentostatin;

• Determine the single and multiple dose pharmacokinetics (PK) of cordycepin given 1 hour after a fixed dose of pentostatin;

• Assess cordycepin pharmacodynamics by measurement of blast cell apoptosis from peripheral blood smears;

• Measure and quantitate any clinical responses in refractory TdT-positive leukemia patients following cordycepin/pentostatin administration.

In the second phase, the Study Objectives are to assess the safety, PK, and clinical outcomes of cordycepin in combination with pentostatin, at the RD, in a 20 subject cohort

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 44
• Est. completion date: December 2010
• Est. primary completion date: December 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• TdT-positive leukemia (ALL, AML, or blastic CML) that has failed at least one standard treatment regimen and for which no standard therapies are expected to result in durable remission. Leukemia is minimally defined as at least 20% blast cells present in marrow or peripheral blood. TdT must be expressed in at least 20% of blast cells present and documented either immunologically or biochemically;

• Age =18 years;

• Must understand and voluntarily sign informed consent;

• Adequate non-hematologic organ system function, defined by:

• Creatinine =1.5 times the upper limit of normal (ULN) and/or creatinine clearance =60 mL/min

• AST and/or ALT =2.5 times upper limit of normal (ULN)

• Total bilirubin within institutional normal range

• Normal EKG and LVEF >40%, measured by EKG and MUGA scan, radionuclide ventriculogram, or echocardiogram

• Life expectancy >3 months;

• Performance status (PS) >70% Karnofsky or ECOG =2;

• Women of childbearing potential must have a negative serum pregnancy test within 7 days of starting study drug. A woman of child-bearing potential is a sexually mature woman who has not undergone a hysterectomy or who has not been naturally postmenopausal for at least 24 consecutive months (i.e., who has had menses at any time in the preceding 24 consecutive months);

• Male or female of child-bearing potential must agree to use adequate contraceptive methods

Exclusion Criteria:

• Failure to meet inclusion criteria;

• Uncontrolled active infection;

• Extramedullary (CNS) disease;

• Serious concomitant medical illness, such as active infection, uncontrolled congestive heart failure, or uncontrolled diabetes or other metabolic disorder, or psychiatric illness;

• Pregnancy or lactation; females of child bearing potential must use adequate contraceptive methods;

• Less than 3 weeks since prior chemotherapy, radiation therapy, or immunotherapy. However, hydroxyurea is permitted up to 24 hours before the study is initiated;

• Less than 2 months following bone marrow or peripheral blood stem cell transplantation or treatment with donor lymphocyte infusion (DLI).

Study Design

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

Related Conditions & MeSH terms

• Leukemia
• Refractory TdT-Positive Leukemia

Intervention

Drug:
• Cordycepin plus Pentostatin
Cordycepin Plus Pentostatin on days 1, 2 and 3 of a 21 day cycle. Number of cycles until progression or unacceptable toxicity

Locations

Country	Name	City	State
United States	Brigham & Women's Hospital	Boston	Massachusetts
United States	Dana Farber Cancer Institute	Boston	Massachusetts
United States	Cancer Therapy Reasearch Center at UTHSCA	San Antonio	Texas

Sponsors (2)

Lead Sponsor	Collaborator
OncoVista, Inc.	AAIPharma

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Establishment of the recommended dose (RD) of cordycepin, given one hour following a fixed dose of the ADA inhibitor pentostatin, in subjects with refractory TdT-positive leukemia		one year	No
Secondary	Determination of the single and multiple dose pharmacokinetics of cordycepin. Measurement and quantification any any clinical responses following administration of cordycepin/pentostatin at the recomme		18 months	No