Skip to content

Efficacy and Safety of Sublingual Fentanyl Tablets in Treatment of Breakthrough Pain in Cancer Patients.

A Double-Blind, Randomized, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of EN3267 for the Treatment of Breakthrough Pain in Opioid Tolerant Cancer Patients.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00262678
Enrollment
Unknown
Registered
2005-12-07
Start date
2005-12-31
Completion date
2009-01-31
Last updated
2009-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Pain

Brief summary

The purpose of this study is to determine the effectiveness and safety of sublingual fentanyl tablets in relieving breakthrough pain in cancer patients.

Interventions

DRUGEN3267

Sponsors

Kyowa Kirin Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
17 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Males or females 17 years of age or older * Stable cancer-related pain. * Are receiving a stable, fixed-schedule oral opioid regimen equivalent to 60 to 1000 mg of oral morphine per day or transdermal fentanyl therapy equivalent to 50 to 300 µg/h, and are on a stable dose of opioid medication for relief of breakthrough pain for at least 14 days prior to screening. * Experiencing 1-4 episodes of breakthrough pain per day. * Meet the criteria defined in the Eastern Cooperative Oncology Group (ECOG) Performance Status for Grade 0, 1, or 2.

Exclusion criteria

* Are pregnant or lactating. * Have uncontrolled or rapidly escalating pain. * Have moderate to severe ulcerative mucositis. * Have a cardiopulmonary disease that would increase the risk of administering potent opioids. * Have neurologic or psychologic disease that would compromise data collection * Have any clinically significant condition that would, in the investigator's opinion, preclude study participation. * Are currently taking monoamine oxidase inhibitors (MAOIs), or have taken MAOIs within 14 days prior to enrolling in the study. * Have received strontium 89 therapy within 60 days prior to entering the study. * Have received anti-neoplastic therapy within 2 weeks of study entry that, in the investigator's opinion, will influence assessment of breakthrough pain * Have received any investigational drug (non-approved) within 30 days prior to the first dose of study medication, or are scheduled to receive an investigational drug other than EN3267 during the course of the study. * Have hypersensitivities, allergies, or contraindications to fentanyl. * Have a significant prior history of substance abuse or alcohol abuse. * May have difficulty complying with the protocol, as assessed by the investigator.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026