Clinical Trials Directory

Trials / Completed

CompletedNCT00780052

Infusional C-myb ASODN in Advanced Hematologic Malignancies

Infusional C-myb Antisense Oligodeoxynucleotide in Advanced Hematological Malignancies

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Abramson Cancer Center at Penn Medicine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate whether C-myb Antisense (AS) Oligonucleotides (ODNs)is a possible treatment modality for advanced hematologic malignancies.

Conditions

Interventions

TypeNameDescription
DRUGc-myb AS ODNSubjects will be admitted to the hospital to receive c-myb AS ODN as a 24-hour continuous intravenous infusion over 7 days. Dose level is increased with each new subject to determine if there is a MTD.

Timeline

Start date
2002-09-01
Primary completion
2011-08-01
Completion
2011-08-01
First posted
2008-10-27
Last updated
2016-09-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00780052. Inclusion in this directory is not an endorsement.

Infusional C-myb ASODN in Advanced Hematologic Malignancies (NCT00780052) · Clinical Trials Directory