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| ID | Type | Description | Link |
|---|---|---|---|
| U54DA037842 | U.S. NIH Grant/Contract | View source |
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The study was discontinued by the sponsor. No results to report
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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
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Healthy adult men who abuse opioids and are physically dependent on them will be invited to participate in a study to examine the ability of NT-814, a neurokinin (NK) antagonist at the 1 and 3 receptor subtypes, to alter the abuse liability of oxycodone.
After completing the screening process, participants will be scheduled for admission onto the General Clinical Research Unit on 5-South for a 13-week study. During Week 1, participants will be detoxified from opioids. During Week 2 after the detoxification period, participants will be randomized to receive one of four maintenance doses of NT-814. During Weeks 3-4 participants may receive oxycodone during laboratory sessions and will complete a cue exposure session involving presentation of neutral and drug cues. Participants then will have the opportunity to self-administer drug by making clicks on a computer mouse. Weeks 2, 5, 8, and 11 will be medication stabilization weeks following by testing during Weeks 3-4, 6-7, 9-10, and 12-13. At the conclusion of the study, participants will be given an exit interview during which the study will be described. Those who are interested in treatment for their drug use at the end of the study will be offered referrals to studies at our Substance Treatment and Research Service or other treatment providers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | Placebo Comparator: Placebo - During this arm, Placebo medication will be administered orally each evening at 8pm. |
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| NT-814 50 mg | Active Comparator | Active Comparator: NT-814 50 mg - During this arm, 50 mg NT-814 will be administered orally each evening at 8pm. |
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| NT-814 100 mg | Active Comparator | Active Comparator: NT-814 100 mg - During this arm, 100 mg NT-814 will be administered orally each evening at 8pm. |
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| NT-814 200 mg | Active Comparator | Active Comparator: NT-814 200 mg - During this arm, 200 mg NT-814 will be administered orally each evening at 8pm. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Placebo | Drug | Placebo for Neurokinin 1,3 antagonist |
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| Measure | Description | Time Frame |
|---|---|---|
| Percentage of oxycodone choices | Percentage of drug (versus money) choices in each study arm will be our primary outcome measure. | 1 week |
| Average visual analog scale ratings of "I like the choice" | Average ratings of oxycodone liking in each study arm will be obtained. | 1 week |
| Measure | Description | Time Frame |
|---|---|---|
| Average visual analog scale ratings of "I want heroin" | Average ratings of "I want heroin" in each study arm will be obtained. | 1 week |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sandra D Comer, PhD | NYSPI and Columbia University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| New York State Psychiatric Institute | New York | New York | United States |
Data will be shared via posters and talks at local and national conferences, as well as in publication form. The sharing of raw data will be done by request only, providing that there is a justifiable reason with a clear hypothesis and data analysis plan.
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Feb 18, 2016 | Jul 31, 2020 | Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Feb 18, 2016 | Jul 31, 2020 | SAP_001.pdf |
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| ID | Term |
|---|---|
| D009293 | Opioid-Related Disorders |
| ID | Term |
|---|---|
| D000079524 | Narcotic-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
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| NT-814 50 mg | Drug | Neurokinin 1,3 antagonist 50 mg |
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| NT-814 100 mg | Drug | Neurokinin 1,3 antagonist 100 mg |
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| NT-814 200 mg | Drug | Neurokinin 1,3 antagonist 200 mg |
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