Skip to content

A Study Using fMRI Imaging to Evaluate the Effect of NKTR-181 on Brain Activity in Healthy, Non-physically Dependent Recreational Opioid Users.

TerminatedPhase 1NCT03802227
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

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 main purpose of this study is to evaluate the effect of NKTR-181 on brain activity in healthy, non-physically dependent recreational opioid users. This study will last about 88 days for each participant.

Study details

Official title
A Phase 1 Double-Blind, Double-Dummy, Parallel-Group, Randomized, Positive Control Study Using fMRI to Evaluate the Effect of NKTR-181 on Brain Activity in Healthy, Non-physically Dependent Recreational Opioid Users
Conditions
  • Moderate to Severe Chronic Pain
Interventions
  • Drug: NKTR-181
  • Drug: Oxycodone IR
Sponsor
Nektar Therapeutics
Start date
2018-10-22
Primary completion
2019-12-17
Sex
All
Age range
from 18 Years to 60 Years
Healthy volunteers
true
Results posted
Yes, on ClinicalTrials.gov
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Key Inclusion Criteria: * Healthy male and female recreational opioid users, 18-65 years of age inclusive. * Body Mass Index (BMI) between 19.0 to 45.0kg/m2 * Have at least one urine drug screen positive for opioids during Screening to confirm recreational opioid use. Subjects testing positive for methadone or buprenorphine prescribed for treatment will be excluded. * Subjects must agree to practice adequate contraception as outlined in the protocol. Key Exclusion Criteria: * Any metal fragments or other bodily metal that would pose a risk to subjects during MRI scanning as determined by the MRI technologist and/or MRI physicist * Any clinically significant disease or condition that might compromise the cardiovascular, hematological, renal, hepatic, pulmonary, endocrine, central nervous, or gastrointestinal systems or other conditions that may interfere with the absorption, distribution, metabolism, or excretion of the study drug or would place the subject at increased risk * History of clinically significant acute asthma or other obstructive airway disease requiring daily controller medication or any condition that may increase the risk for respiratory depression * Current neurologic conditions such as convulsive disorders, or history of severe head injury. * Any current DSM-5 axis I psychiatric disorder or neurological disorder requiring ongoing treatment * Current substance use disorder (moderate to severe), other than Opioid, Nicotine, THC (tetrahydrocannabinol), cocaine, or caffeine as defined by DSM-5 * Physical dependence of opioids * History of claustrophobia or any other psychiatric disorder that would preclude subject tolerance of MRI procedures. * Current use of any medication that could affect central nervous system blood flow (e.g. certain cardiovascular medications, triptan migraine medications) * Clinical Opiate Withdrawal Scale (COWS) score of greater than 5 during screening or prior to first scan. * Positive urine drug screen for buprenorphine or methadone immediately prior to the first scan.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03802227