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[11C]-NOP46 PET/CT Scan for Chronic Pain
Phase < 1
Recruiting
Led By Akiva Mintz, MD, PhD
Research Sponsored by Akiva Mintz
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
For Patients with Focal Pain: Subjects must have current pain from a focal injury for which they are under a physician's care.
All subjects must be 18 years of age or older, able to read, understand, and voluntarily sign an informed consent document.
Must not have
Participants with evidence of diffuse pain at the time of enrollment up to agent administration are to be excluded from this study.
Women who are pregnant or breastfeeding.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 48 hours post-scan
Awards & highlights
No Placebo-Only Group
Summary
This trial involves giving a small amount of a new drug called [11C]-NOP46 to people with long-term pain. The drug travels to the painful areas in the body, and a camera takes pictures of these areas. This could help doctors better understand and treat long-term pain.
Who is the study for?
This trial is for adults who can consent to participate. Healthy volunteers must not have chronic pain or be pregnant, and agree to use contraception. Patients with focal pain should experience moderate to severe pain (>4 on the Visual Analogue Scale) and also agree to contraceptive measures.
What is being tested?
The study tests a new radiotracer called [11C]-NOP46 using PET/CT scans in two stages: first in five healthy individuals for safety, then in thirty patients with chronic pain if no toxicities are found.
What are the potential side effects?
Potential side effects aren't specified but will be monitored during the initial safety evaluation of the radiotracer [11C]-NOP46 in healthy participants before proceeding with patients having chronic pain.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am currently experiencing pain from a specific injury and am seeing a doctor for it.
Select...
I am 18 or older and can understand and sign a consent form.
Select...
I am a volunteer without any ongoing pain from an injury.
Select...
My pain level is more than 4 on a scale of 0 to 10.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not have widespread pain currently.
Select...
I am not pregnant or breastfeeding.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 48 hours post-scan
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~48 hours post-scan
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Uptake ratio for site with pain is >1
Secondary study objectives
Occurrence of Physiologic Effects of Single Micro-dose of [11C]-NOP46
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Individuals with Focal PainExperimental Treatment2 Interventions
In Stage 2, up to 30 subjects with focal pain will receive a microdose of \[11C\]-NOP46 and undergo PET/CT scans for up to 60 minutes in length. The results of Stage 1 will inform the scanning parameters (uptake period, scan length, reconstruction parameters, etc.) for Stage 2.
Group II: Healthy VolunteersExperimental Treatment2 Interventions
In Stage 1, five healthy volunteers will receive a microdose of \[11C\]-NOP46 and undergo serial whole body PET/CT scans for up to 240 minutes post-administration. These image sets will be used to evaluate \[11C\]-NOP46 biodistribution and derive dosimetry estimates.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
PET/CT scan
2013
Completed Phase 1
~340
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for chronic pain work through various mechanisms. Pharmacologic treatments like NSAIDs and acetaminophen reduce inflammation and inhibit pain signals, while antidepressants and anticonvulsants modulate neurotransmitter levels to alleviate neuropathic pain.
Psychological therapies, such as cognitive-behavioral therapy, help patients manage pain perception and improve coping strategies. Interventional approaches, including radiopharmaceuticals, target specific pain pathways and provide localized pain relief.
Understanding these mechanisms is crucial for chronic pain patients as it allows for personalized treatment plans that can improve efficacy and reduce side effects. Radiotracers like [11C]-NOP46 used in PET/CT imaging help visualize pain pathways, aiding in the precise targeting of treatments.
Optimizing and Accelerating the Development of Precision Pain Treatments for Chronic Pain: IMMPACT Review and Recommendations.Challenges and opportunities in translational pain research - An opinion paper of the working group on translational pain research of the European pain federation (EFIC).Central Nervous System Targets: Supraspinal Mechanisms of Analgesia.
Optimizing and Accelerating the Development of Precision Pain Treatments for Chronic Pain: IMMPACT Review and Recommendations.Challenges and opportunities in translational pain research - An opinion paper of the working group on translational pain research of the European pain federation (EFIC).Central Nervous System Targets: Supraspinal Mechanisms of Analgesia.
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Who is running the clinical trial?
Akiva MintzLead Sponsor
Akiva Mintz, MD, PhDPrincipal Investigator - Columbia University
Columbia University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I agree to use birth control or abstain from sex during the study.I do not have widespread pain currently.I am currently experiencing pain from a specific injury and am seeing a doctor for it.I am not pregnant or breastfeeding.You cannot handle PET/CT scans.I cannot stop taking my pain medication for 2 days before receiving the study treatment.I am 18 or older and can understand and sign a consent form.I am a volunteer without any ongoing pain from an injury.I am not pregnant or capable of becoming pregnant.I am not pregnant and can prove it with a test if I am capable of becoming pregnant.My pain level is more than 4 on a scale of 0 to 10.
Research Study Groups:
This trial has the following groups:- Group 1: Individuals with Focal Pain
- Group 2: Healthy Volunteers
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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