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Spots Global Cancer Trial Database for Safety and Tolerability of Egalet-002 in Patients With Moderate-to-Severe Chronic Noncancer Pain

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

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

Official Title: An Open-label Phase 3 Trial to Evaluate the Safety and Tolerability of Egalet ADER Oxycodone Tablet, Egalet-002, in Patients With Moderate-to-Severe Chronic Noncancer Pain

Study ID: NCT02603705

Study Description

Brief 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.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Site 334, Huntsville, Alabama, United States

Site 328, Tucson, Arizona, United States

Site 332, Jacksonville, Florida, United States

Site 340, Miami Gardens, Florida, United States

Site 320, Plantation, Florida, United States

Site 302, Tampa, Florida, United States

Site 315, Tampa, Florida, United States

Site 310, Winter Haven, Florida, United States

Site 316, Dawsonville, Georgia, United States

Site 311, Marietta, Georgia, United States

Site 336, Bloomington, Illinois, United States

Site 345, Blue Island, Illinois, United States

Site 304, Evansville, Indiana, United States

Site 325, Valparaiso, Indiana, United States

Site 321, Overland Park, Kansas, United States

Site 342, Wichita, Kansas, United States

Site 329, New Orleans, Louisiana, United States

Site 326, Quincy, Massachusetts, United States

Site 303, Saint Louis, Missouri, United States

Site 306, Las Vegas, Nevada, United States

Site 313, Belvidere, New Jersey, United States

Site 346, Blackwood, New Jersey, United States

Site 323, Hartsdale, New York, United States

Site 338, Mooresville, North Carolina, United States

Site 333, Cincinnati, Ohio, United States

Site 343, Cleveland, Ohio, United States

Site 308, Huber Heights, Ohio, United States

Site 347, Kettering, Ohio, United States

Site 335, Oklahoma City, Oklahoma, United States

Site 312, Eugene, Oregon, United States

Site 322, Duncansville, Pennsylvania, United States

Site 324, Wyomissing, Pennsylvania, United States

Site 344, Myrtle Beach, South Carolina, United States

Site 314, Summerville, South Carolina, United States

Site 341, New Tazewell, Tennessee, United States

Site 318, Austin, Texas, United States

Site 330, Dallas, Texas, United States

Site 309, San Antonio, Texas, United States

Site 331, West Jordan, Utah, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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