Skip to main content
Clinical Trials/NCT00915083
NCT00915083
Completed
Phase 1

A Phase I Study to Assess the Safety, Pharmacokinetics, and Potential Effects of Amrubicin on the QT/QTc Interval in Cancer Patients With Advanced Solid Tumors.

Celgene8 sites in 1 country24 target enrollmentJune 1, 2009
InterventionsAmrubicin

Overview

Phase
Phase 1
Intervention
Amrubicin
Conditions
Advanced Solid Tumors
Sponsor
Celgene
Enrollment
24
Locations
8
Primary Endpoint
To characterize the pharmacokinetics of amrubicin and amrubicinol (metabolite) in plasma, whole blood, and urine in patients given amrubicin as 5 minute IV infusions at 40 mg/m2 for 3 consecutive days; data will be obtained from blood & urine samples
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of the study is to determine whether amrubicin is safe and effective in the treatment of patients with advanced solid tumors. The study will assess the pharmacokinetics of the amrubicin and if it has an effect on the heart.

Registry
clinicaltrials.gov
Start Date
June 1, 2009
End Date
May 1, 2011
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Celgene
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients meeting all of the following criteria will be considered for enrollment into the study:
  • Males or females, aged 18-65 years;
  • Histological or cytological diagnosis of solid malignancy for which no acceptable standard therapy exists or for which approved standard therapy has failed;
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1;
  • Life expectancy greater than 3 months;
  • Nonsmoker or not smoked or used tobacco products for at least 3 months before the screening visit and agree to abstain from smoking/using tobacco products throughout the formal study and until the End of Study visit;
  • Capable of giving informed consent, has signed the informed consent form, and is willing to comply with scheduled visits, dose administration, and other study procedures;
  • Women of childbearing potential may participate, providing they have a negative serum pregnancy test (β-HCG) at screening, and a negative urine pregnancy test prior to dosing on Day 1 of each cycle;
  • Males and females of childbearing potential must agree to the use of at least 2 effective contraceptive methods until at least 28 days following the last dose of study drug;
  • Serum potassium, magnesium and corrected calcium that is within institutional normal range at screening;

Exclusion Criteria

  • Patients meeting any of the following criteria will be excluded from the study:
  • Hypersensitivity to amrubicin or related compounds;
  • Radiotherapy with curative intent to a primary disease complex ≤ 28 days before first dose; cranial radiotherapy ≤ 21 days before first dose; radiotherapy to all other areas ≤ 7 days before first dose of amrubicin;
  • History or presence of clinically significant abnormal 12-lead ECG or triplicate ECGs with a mean QT interval corrected for heart rate (HR) using Fridericia's method (QTcF) of \>450 msec (males) or \>470 msec (females), a PR interval \>240 msec or a QRS interval \>110 msec (within 3 months of screening visit);
  • Left ventricular ejection fraction (LVEF) \<50%;
  • Recent history (within 3 months of screening visit) of pericarditis and pericardial effusion;
  • History within 6 months of the screening visit of one of the following:
  • cardiac disease including congenital long-QT syndrome,
  • angina, congestive heart failure,
  • myocardial ischemia or infarction,

Arms & Interventions

Amrubicin 40mg/m^2

Amrubicin 40mg/m\^2 given as a 5 minute IV infusion on Days 1, 2 \& 3 of a 21 day cycle

Intervention: Amrubicin

Outcomes

Primary Outcomes

To characterize the pharmacokinetics of amrubicin and amrubicinol (metabolite) in plasma, whole blood, and urine in patients given amrubicin as 5 minute IV infusions at 40 mg/m2 for 3 consecutive days; data will be obtained from blood & urine samples

Time Frame: Cycle 1: all primary outcome measures are collected during the first 21 days.

The duration of making measurements during the first cycle is 21 days. All data relating to the primary outcome measure is collected during this time. There is an optional Extension Phase during which subjects can continue to receive additional 21-day cycles of amrubicin unless there is evidence of tumor progression or unacceptable toxicity. The duration of measurements depends on how long the subject continues on treatment.

To determine the safety and tolerability of 40 mg/m2 amrubicin given as 5 minute IV infusions for 3 consecutive days; information will be collected by adverse event monitoring and laboratory safety tests.

Time Frame: Cycle 1: all primary outcome measures are collected during the first 21 days.

The duration of making measurements during the first cycle is 21 days. All data relating to the primary outcome measure is collected during this time. There is an optional Extension Phase during which subjects can continue to receive additional 21-day cycles of amrubicin unless there is evidence of tumor progression or unacceptable toxicity. The duration of measurements depends on how long the subject continues on treatment.

To evaluate the potential effects on the QT/QTc interval in cancer patients when treated with 5 minute IV infusions of amrubicin 40 mg/m2 daily for 3 consecutive days; data will be obtained by ECG extraction from continuous 12-lead Holter monitoring

Time Frame: Cycle 1: all primary outcome measures are collected during the first 21 days.

The duration of making measurements during the first cycle is 21 days. All data relating to the primary outcome measure is collected during this time. There is an optional Extension Phase during which subjects can continue to receive additional 21-day cycles of amrubicin unless there is evidence of tumor progression or unacceptable toxicity. The duration of measurements depends on how long the subject continues on treatment.

Secondary Outcomes

  • 1. Explore the relationship between pharmacokinetics and QTc interval change. Information will be obtained by further analysis of the datasets obtained from the primary outcome measures(Cycle 1: all primary outcome measures are collected during the first 21 days.)

Study Sites (8)

Loading locations...

Similar Trials