CClinicalTrials.gg
CompletedNCT02603705Updated Mar 5, 2018

Safety and Tolerability of Egalet-002 in Patients With Moderate-to-Severe Chronic Noncancer Pain

A Phase 3 interventional study of Oxycodone extended-release in Moderate-to-severe Chronic Noncancer Pain, sponsored by Egalet Ltd. Completed at 39 sites in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2018-03-05.

Sponsored by Egalet Ltd · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
281
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the safety and tolerability of Egalet-002 in opioid-experienced patients with moderate-to-severe chronic noncancer pain.

02

Conditions studied

  • Moderate-to-severe Chronic Noncancer Pain

Keywords

  • chronic pain
  • opioid
  • oxycodone
  • non cancer pain
  • moderate to severe
03

In context

Lead sponsor

Egalet Ltd is the lead sponsor of 18 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Is a man or woman between 18 and 75 years of age.
  • Has a clinical history of moderate-to-severe chronic noncancer pain ≥6 months.
  • Has required opioid therapy for at least 14 days prior to Screening at a dose between 20 mg and 160 mg (inclusive) oxycodone/day (or opioid equivalent), and will, in the opinion of the investigator, continue to require opioid therapy (between 20 mg and 240 mg oxycodone/day, inclusive) for management of moderate-to-severe pain for the duration of the study.
  • Has pain either not adequately controlled on current opioid regimen, requires a change of opioid due to tolerability of current opioid regimen or in the opinion of the investigator, would benefit from changing opioid for another reason.
  • Has stable health, as determined by the investigator.
  • If female, the patient is currently not pregnant, not breast-feeding, nor attempting to become pregnant (for 30 days before screening through the duration of the study), or is of non-childbearing potential.
  • Other Criteria Apply

Exclusion criteria

Exclusion Criteria:

  • Has cancer-related pain.
  • Is receiving >240 mg oxycodone daily (or opioid equivalent) within 30 days before Screening.
  • Has a history of attempted suicide.
  • Has used a spinal infusion pump within 6 months before Screening.
  • Has clinically unstable cardiac disease (including atrial fibrillation, symptomatic bradycardia, unstable congestive heart failure, or active myocardial ischemia) and/or respiratory disease (including chronic obstructive pulmonary disease or sleep apnea).
  • Has positive urine toxicity screen for drugs of abuse (with the exception of prescribed medications).
  • Has positive result for tetrahydrocannabinol (even if legally prescribed).
  • Has current (or history of within the last 12 months) drug dependence or substance abuse disorder according to Diagnostic and Statistical Manual of Mental Disorders, 5th Edition, Text Revision criteria (excluding nicotine).
  • Other Criteria Apply
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
281 participants (actual)

Study arms

  • Experimental
    Oxycodone extended-release

    Egalet abuse-deterrent, extended-release oxycodone tablet

    Drug: Oxycodone extended-release

Interventions

  • DrugOxycodone extended-release
06

What researchers measure

Primary outcomes

  1. Incidence of TEAEs during the Open-label Treatment Period, including those leading to treatment withdrawal, and/or abnormal physical examination findings, vital signs measurements, ECGs, and clinical laboratory test results, related to treatment

    Time frame: 1 year

Secondary outcomes

  1. Findings of the Brief Pain Inventory-Short Form (BPI-SF) during the Open-label Treatment Period

    Time frame: 1 year

07

Study locations

39 sites
  • Site 334
    Huntsville, Alabama 35801, United States
  • Site 328
    Tucson, Arizona 85712, United States
  • Site 332
    Jacksonville, Florida 32257, United States
  • Site 340
    Miami Gardens, Florida 33169, United States
  • Site 320
    Plantation, Florida 33317, United States
  • Site 302
    Tampa, Florida 33603, United States
  • Site 315
    Tampa, Florida 33613, United States
  • Site 310
    Winter Haven, Florida 33880, United States
  • Site 316
    Dawsonville, Georgia 30534, United States
  • Site 311
    Marietta, Georgia 30060, United States
  • Site 336
    Bloomington, Illinois 61701, United States
  • Site 345
    Blue Island, Illinois 60406, United States
  • Site 304
    Evansville, Indiana 47714, United States
  • Site 325
    Valparaiso, Indiana 46383, United States
  • Site 321
    Overland Park, Kansas 66210, United States
  • Site 342
    Wichita, Kansas 67205, United States
  • Site 329
    New Orleans, Louisiana 70114, United States
  • Site 326
    Quincy, Massachusetts 02169, United States
  • Site 303
    Saint Louis, Missouri 63141, United States
  • Site 306
    Las Vegas, Nevada 89119, United States
  • Site 313
    Belvidere, New Jersey 07823, United States
  • Site 346
    Blackwood, New Jersey 08012, United States
  • Site 323
    Hartsdale, New York 10530, United States
  • Site 338
    Mooresville, North Carolina 28117, United States
  • Site 333
    Cincinnati, Ohio 45212, United States
  • Site 343
    Cleveland, Ohio 44122, United States
  • Site 308
    Huber Heights, Ohio 45424, United States
  • Site 347
    Kettering, Ohio 45429, United States
  • Site 335
    Oklahoma City, Oklahoma 73112, United States
  • Site 312
    Eugene, Oregon 97401, United States
  • Site 322
    Duncansville, Pennsylvania 16635, United States
  • Site 324
    Wyomissing, Pennsylvania 19610, United States
  • Site 344
    Myrtle Beach, South Carolina 29588, United States
  • Site 314
    Summerville, South Carolina 29485, United States
  • Site 341
    New Tazewell, Tennessee 37825, United States
  • Site 318
    Austin, Texas 78731, United States
  • Site 330
    Dallas, Texas 75231, United States
  • Site 309
    San Antonio, Texas 78218, United States
  • Site 331
    West Jordan, Utah 84088, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02603705
Lead sponsor
Egalet Ltd
Responsible party
Sponsor
First posted
Nov 13, 2015
Start date
Mar 7, 2016
Primary completion
Jun 15, 2017
Completion
Jun 15, 2017
Last update
Mar 5, 2018

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2018. You cannot join it, but the record below documents what was studied.

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