A Long-term Safety Study With Tapentadol ER and Oxycodone CR in Patients With Moderate to Severe Pain Due to Chronic, Painful Diabetic Peripheral Neuropathy (DPN)

Stopped early · Phase 3

Conditions studied: Diabetic Neuropathy, Painful, Diabetic Polyneuropathy

In brief

The purpose of this study is to evaluate the safety profile of orally administered tapentadol ER dosages of 100 to 250 mg twice daily in patients with chronic, painful diabetic peripheral neuropathy (DPN) over long-term exposure of up to 1 year.

Key facts

Study ID

NCT01063868

Run by

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

People needed

47

Starts

2010-01-01

Expected to finish

2010-06-01

Last updated by the study team

2014-03-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Man or woman aged 18 years or older
• Patients with Type 1 or 2 diabetes mellitus must have a documented clinical diagnosis of painful diabetic peripheral neuropathy with symptoms and signs for at least 6 months, and pain present at the time of screening
• Diagnosis must include pain plus reduction or absence of pin sensibility and/or vibration sensibility on Total Neuropathy Score - Nurse (TNSn) examination in lower and/or upper extremities at screening
• The investigator considers the patient's blood glucose to be controlled by diet, or hypoglycemics, or insulin for at least 3 months prior to enrolling in the study (this control should be documented by figures of glycated hemoglobin (HbA1c) no greater than 11% at screening)
• Patients have been taking analgesic medications for the condition for at least 3 months prior to screening (patients taking opioid analgesics must be dissatisfied with current treatment, and patients taking non-opioid analgesics must be dissatisfied with current analgesia)
• Patients currently requiring opioid treatment must be taking daily doses of an opioid-based analgesic equivalent to <=160mg of oral morphine
• Patients with baseline score for average pain intensity in the previous 24 hours of =>4 on the 11-point numerical rating scale (NRS) at the beginning of the titration period

You may not qualify if…

• Significant pulmonary, gastrointestinal, endocrine, metabolic (except diabetes mellitus), neurological, psychiatric disorders (resulting in disorientation, memory impairment or inability to report accurately as in schizophrenia, Alzheimer's disease)
• History of moderate to severe hepatic impairment
• Severely impaired renal function
• Clinically significant laboratory abnormalities
• Clinically significant cardiac disease
• History of seizure disorder or epilepsy
• History of any other clinically significant disease that in the investigator's opinion may affect efficacy or safety assessments or may compromise patient safety during study participation.

Where it is running

• Study site — Mesa, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Fruitland Park, Florida, United States
• Study site — New Port Richey, Florida, United States
• Study site — Oviedo, Florida, United States
• Study site — Tampa, Florida, United States
• Study site — Libertyville, Illinois, United States
• Study site — Franklin, Indiana, United States
• Study site — Paducah, Kentucky, United States
• Study site — Wellesley Hills, Massachusetts, United States
• Study site — Albuquerque, New Mexico, United States
• Study site — New York, New York, United States
• Study site — Greenville, North Carolina, United States
• Study site — Hickory, North Carolina, United States
• Study site — Wilmington, North Carolina, United States
• Study site — Winston-Salem, North Carolina, United States
• Study site — Kettering, Ohio, United States
• Study site — Tulsa, Oklahoma, United States
• Study site — Greer, South Carolina, United States
• Study site — Dallas, Texas, United States
• Study site — Odessa, Texas, United States
• Study site — San Antonio, Texas, United States
• Study site — Virginia Beach, Virginia, United States

Full record on ClinicalTrials.gov

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