Clinical Trials Directory

Trials / Completed

CompletedNCT00293020

Study of the Safety of BEMA™ Fentanyl Use for Breakthrough Pain in Cancer Subjects on Chronic Opioid Therapy

An Open Label, Long-term Treatment Evaluation of the Safety of BEMA™ Fentanyl Use for Breakthrough Pain in Cancer Subjects on Chronic Opioid Therapy

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
244 (actual)
Sponsor
BioDelivery Sciences International · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety of BEMA fentanyl at any dose in the management of breakthrough pain in cancer subjects on background opioid therapy. The standard of care for these breakthrough pain episodes is a rapid onset, short acting analgesic with minimal associated sleepiness. Oral morphine, oxycodone and hydromorphone are routinely used, but because of slow and variable oral absorption, the pain control is not the best with these products. Oral transmucosal fentanyl citrate (OTFC) has been used successfully in treating breakthrough pain episodes associated with cancer. OTFC is a lozenge of fentanyl on a stick and is administered by continuously swabbing the interior of the subject's mouth until the product is dissolved (approximately 15 to 30 minutes). The buccal route of administration avoids the delay and variability associated with oral absorption. BioDelivery Sciences International, Inc. (BDSI) has developed BEMA (BioErodible MucoAdhesive) fentanyl, an alternative product to OTFC that does not require the subject to continuously paint the inside of the mouth with the dosage form. The BDSI product is a small disc that is placed against the mucosal membrane inside the mouth. The mucoadhesive polymers in the disc readily adhere to the mucosal membrane (within 5 seconds) when moistened. The components of the disc are water soluble, so the entire dosage form dissolves within 30 minutes of application.

Conditions

Interventions

TypeNameDescription
DRUGBEMA Fentanylbuccal soluble film; 200, 400, 600, 800, 1200 mcg fentanyl; up to 4 times daily

Timeline

Start date
2006-02-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2006-02-17
Last updated
2012-10-05
Results posted
2012-10-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00293020. Inclusion in this directory is not an endorsement.