Study of COV795 in Subjects With Osteoarthritis or Chronic Low Back Pain
CompletedPhase 3NCT01451385
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The primary objective is to demonstrate the safety and tolerability of COV795 with up to 35 days use as evaluated by physical exam, vital signs, pulse oximetry, clinical laboratory tests, and other adverse events (AEs).
Study details
- Official title
- An Open Label Safety Study of COV795 in Subjects With Osteoarthritis or Chronic Low Back Pain
- Conditions
- Interventions
- Drug: COV795
- Sponsor
- Mallinckrodt
- Start date
- 2011-09-20
- Primary completion
- 2012-06-18
- Sex
- All
- Age range
- from 18 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- United States
- Total sites listed
- 42
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion 1. Be considered in general good health based upon medical and surgical history, vital signs, pulse oximetry, physical exam, clinical lab tests, and electrocardiogram (ECG). 2. Be ≥18 years of age 3. Female subjects are eligible if not pregnant, not lactating or not planning to become pregnant within the next 2 months; surgically sterile or at least 2 years postmenopausal, or practicing an acceptable form of birth control for the duration of the study 4. Male subjects biologically capable of having children must agree to the use of a reliable method of birth control for the duration of the study 5. Have a clinical diagnosis of one of the following: * Osteoarthritis (OA) of the knee or hip for at least one year based on the American College of Rheumatology (ACR) criteria * Moderate to severe chronic lower back pain (CLBP), i.e. pain that occurs in an area with boundaries between the lowest rib and the crease of the buttocks that 1) must have been present for at least several hours a day for a minimum of 3 months, 2) is not due to a known malignancy, and 3) must be classified as non-neuropathic, neuropathic, or symptomatic for more than 6 months after lower back pain (LBP) surgery based on the Quebec Task Force Classification of Spinal Disorders 6. Have an average in-clinic pain score of ≥3 on the 11-point (0-10) numerical rating scale (NRS) as an average for the last 24 hours at screening visit. 7. Have a pain intensity score of ≥4 on NRS as an average for the last 24 hours at baseline visit. 8. Must, in the investigator's opinion, qualify for opioid therapy for their CLBP or OA. 9. Voluntarily provide written informed consent. Exclusion 1. Have any clinically significant condition or unstable inter-current illness that would preclude study participation or interfere with the assessment of pain and other symptoms of CLBP or OA or would increase the risk of opioid-related AEs 2. Have an uncontrolled or poorly controlled major psychiatric condition, or have clinically significant anxiety or depression 3. Have an active malignancy or history of malignancy within 2 years 4. Have a history of seizures (except pediatric febrile seizures) or cognitive dysfunction 5. Have clinically significant ECG abnormalities or have uncontrolled hypo- or hypertension 6. Had arthroscopic or open surgery on either knee or hip selected as the primary OA study joint within 6 months 7. For CLBP, had a surgical procedure for back pain within 6 months 8. For CLBP participant…
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01451385