A Study to Determine the Efficacy and Safety of Fasinumab for the Treatment of Adults With Chronic Low Back Pain



Status:Completed
Conditions:Back Pain, Back Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:35 - Any
Updated:2/10/2018
Start Date:January 26, 2016
End Date:September 13, 2017

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A Randomized, Double-blind, Multi-dose, Placebo-controlled Phase 2/3 Study to Evaluate the Efficacy and Safety of Fasinumab in Patients With Moderate to Severe Chronic Low Back Pain

The main objective of the trial is to evaluate the efficacy of fasinumab compared to placebo
as measured by the change from baseline in the average daily Low Back Pain Intensity (LBPI)
Numerical Rating Scale (NRS).

Secondary objectives of the study are to evaluate the efficacy of fasinumab compared to
placebo as measured by:

- Change from baseline in the Roland Morris disability questionnaire (RMDQ) total score

- Change from baseline in the Patient Global Assessment (PGA) of Low Back Pain (LBP) score

- Change from baseline in the average daily LBPI NRS score


Key Inclusion Criteria:

1. Male or female ≥35 years of age at the screening visit

2. Clinical diagnosis of chronic moderate to severe LBP (nonradiculopathic)for ≥3 months

3. History of regular analgesic medication

4. History of inadequate pain relief or intolerance to analgesics used for chronic LBP

5. Willing to discontinue current pain medication

Key Exclusion Criteria:

1. History of lumbosacral radiculopathy within the past 2 years

2. Evidence on baseline lumbar spine magnetic resonance imaging of potentially
confounding conditions

3. Recent use of longer acting pain medications

4. Evidence of destructive arthropathy

5. Other medical conditions that may interfere with participation or accurate assessments
during the trial
We found this trial at
59
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