Clinical Trials Directory

Trials / Completed

CompletedNCT01028859

Safety Study of Increasing Doses of CKD-516 in Patients With Advanced Solid Cancers

Phase I Clinical Trial to Assess the Safety and Pharmacokinetic Profile of CKD-516 in Patients With Advanced Solid Cancers Failed to Standard Therapy

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Chong Kun Dang Pharmaceutical · Industry
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

A phase I study is conducted to determine the maximum tolerated dose (MTD), dose limiting toxicity (DLT), safety and pharmacokinetics (PK) profile of a single agent CKD-516 injection on a weekly schedule in patients with advanced solid cancers failed to standard therapy. The usefulness of the this regimen is evaluated by response rate, progression free survival and vascular disruption effect by Dynamic Contrast-Enhanced MRI (DCE-MRI).

Detailed description

OBJECTIVES: * I. Determine the maximum tolerated dose of CKD-516 administered at single doses every 21 days in patients with advanced solid tumors. * II. Determine both the toxicity and dose limiting toxicity of this regimen in these patients. * III. Determine the plasma and urine pharmacokinetics of CKD-516. * IV. Gather preliminary data regarding possible antitumor effects in those patients with measurable diseae. Assess the effects of CKD-516 on tumor blood flow using DCE-MRI scanning techniques, and establish the dose at which these effects occur. OUTLINE: This is an open label, dose escalation study. Patients receive CKD-516 IV over 30 minutes on day 1, 8 every 3 weeks in the absence of unacceptable toxicity or disease progression. Cohorts of 3\~6 patients receive escalating doses of CKD-516 until the maximum tolerated dose(MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose limiting toxicity.

Conditions

Interventions

TypeNameDescription
DRUGCKD-516 inj5.0 mg/2ml; 1.0, 2.0, 3.3, 5, 7, 9 \~ mg/m2; Day 1, Day 8 every 3 weeks

Timeline

Start date
2009-12-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2009-12-09
Last updated
2011-12-22

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01028859. Inclusion in this directory is not an endorsement.