Chronic Pain Master Protocol (CPMP): A Study of LY3016859 in Participants With Chronic Low Back Pain

Completed · Phase 2 · Has a placebo group

Conditions studied: Chronic Low-back Pain

In brief

This study is being done to test the safety and efficacy of the study drug LY3016859 for the treatment of chronic low back pain. This trial is part of the chronic pain master protocol H0P-MC-CPMP (NCT05986292) which is a protocol to accelerate the development of new treatments for chronic pain.

Key facts

Study ID

NCT04529096

Run by

Eli Lilly and Company

People needed

149

Starts

2020-08-25

Expected to finish

2021-10-04

Last updated by the study team

2023-11-30

Who can join

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

You may qualify if…

• Have a visual analog scale (VAS) pain value ≥40 and <95 during screening.
• Have a history of daily pain for at least 12 weeks based on participant report or medical history.
• Have a value of ≤30 on the pain catastrophizing scale.
• Have a body mass index <40 kilograms per meter squared (kg/m²) (inclusive).
• Are willing to maintain a consistent regimen of any ongoing nonpharmacologic pain-relieving therapies (for example, physical therapy) and will not start any new nonpharmacologic pain-relieving therapies during study participation.
• Are willing to discontinue all medications taken for chronic pain conditions for the duration of the study.
• Have a history of low back pain for at least 3 months located between the 12th thoracic vertebra and the lower gluteal folds, with or without radiation.
• Have a history of low back pain as classified by the Quebec Task Force Category 1 through 3.
• Have stable glycemic control as indicated by a glycated hemoglobin (HbA1c) less than or equal to 10 at time of screening.
• Are men, or women able to abide by reproductive and contraceptive requirements.

You may not qualify if…

• Have second- or third-degree atrioventricular (AV) heart block or AV dissociation or history of ventricular tachycardia.
• Have had a procedure within the past 6 months intended to produce permanent sensory loss in the target area of interest (for example, ablation techniques).
• Have surgery planned during the study for any reason, related or not to the disease state under evaluation.
• Have, in the judgment of the investigator, an acute, serious, or unstable medical condition or a history or presence of any other medical illness that would preclude study participation.
• There is an inability to rule out other causative or confounding sources of pain in the primary condition under study.
• Have had cancer within 2 years of baseline, except for cutaneous basal cell or squamous cell carcinoma resolved by excision.
• Have a substance use disorder as defined by the Diagnostic and Statistical Manual of Mental Disorders (5th edition; DSM-5; American Psychiatric Association).
• Have congenital QT prolongation or QT interval corrected for heart rate using Fridericia's formula (QTcF) interval measurement >450 milliseconds (msec) for male participants, >470 msec for female participants, or >480 msec for participants with bundle branch block.
• Have any clinically important abnormality at screening, as determined by investigator, in physical or neurological examination, vital signs, electrocardiogram (ECG), or clinical laboratory test results that could be detrimental to the participant or could compromise the study.
• Have a positive human immunodeficiency virus (HIV) test result at screening.
• Are, in the judgment of the investigator, actively suicidal and therefore deemed to be at significant risk for suicide.
• Have an intolerance to acetaminophen or paracetamol or any of its excipients.
• Have a history of alcohol, illicit drug, analgesic or narcotic use disorder within 2 years prior to screening.
• Have used a therapeutic injection (botulinum toxin or corticosteroids) in the 3 months prior to starting the washout period.
• Have history of or current compression fracture.
• Have had a recent major trauma (within 6 months of baseline).
• Have a history of low back pain as classified by the Quebec Task Force Categories 4 through 11.
• Are using spinal cord stimulator or dorsal root ganglion stimulator.
• Have fibromyalgia.

Where it is running

• Simon Williamson Clinic — Birmingham, Alabama, United States
• Synexus - US — Chandler, Arizona, United States
• Synexus- Chandler — Chandler, Arizona, United States
• Irvine Clinical Research Center — Irvine, California, United States
• Artemis Institute for Clinical Research — Riverside, California, United States
• Artemis Institute for Clinical Research — San Diego, California, United States
• VIN-Julie Schwartzbard — Aventura, Florida, United States
• Suncoast Research Group — Miami, Florida, United States
• Renstar Medical Research — Ocala, Florida, United States
• Synexus - US — Orlando, Florida, United States
• Synexus - US — Pinellas Park, Florida, United States
• Martin E. Hale M.D., P.A. — Plantation, Florida, United States
• Synexus - US — The Villages, Florida, United States
• Synexus Clinical Research — Chicago, Illinois, United States
• Northwestern University — Chicago, Illinois, United States
• Cotton O'Neil Infusion Center — Topeka, Kansas, United States
• ActivMed Practices and Research — Methuen, Massachusetts, United States
• MedVadis Research Corporation — Waltham, Massachusetts, United States
• Great Lakes Research Group, Inc. — Bay City, Michigan, United States
• StudyMetrix Research — City of Saint Peters, Missouri, United States
• Synexus - US — Omaha, Nebraska, United States
• PharmQuest — Greensboro, North Carolina, United States
• Synexus - Cincinnati — Cincinnati, Ohio, United States
• Rapid Medical Research — Cleveland, Ohio, United States
• Aventiv Research Inc — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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