Omnitram Pharmacokinetic and Analgesic Study Following CY2D6 Inhibition With Paroxetine In Healthy Volunteers

Completed · Phase 1 · Has a placebo group

Conditions studied: Pain

In brief

This study evaluates the analgesic effect of Omnitram and tramadol during concurrent administration of paroxetine. Paroxetine administration is expected to diminish the analgesic effect of tramadol, but not Omnitram. Each participant will receive paroxetine before and during treatment with Omnitram, tramadol, and placebo.

Key facts

Study ID

NCT03312777

Run by

Syntrix Biosystems, Inc.

People needed

60

Starts

2017-10-31

Expected to finish

2017-12-22

Last updated by the study team

2017-12-28

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy males and females with normal vital signs: systolic blood pressure > 90 mm Hg and < 140 mm Hg; diastolic blood pressure > 45 mm Hg and < 90 mm Hg; pulse 40 to 100 beats per minute; respiratory rate 10 to 20 breathes per minute.
• Between the ages of 18 and 50 years of age.
• Able and willing to give informed consent
• Able to comply with all study procedures.
• If female, must not be of childbearing potential or must agree to use one or more of the following forms of contraception during screening and for 30 days following study drug administration: hormonal (e.g., oral, transdermal, intravaginal, implant or injection); double barrier (i.e., condom, diaphragm with spermicide); intrauterine device (IUD) or system (IUS); vasectomized partner (6 months minimum); abstinence; or bilateral tubal ligation.
• Have adequate hematologic function as evidenced by the following screening results:
• WBC >3,500/mm3 and < 12,000/mm3 Platelet Count > 150,000/mm3 and < 540,000/mm3 Hemoglobin > 12.0 gm/dL and < 20.5 gm/dL
• Have adequate liver function as evidenced by the following screening results:
• AST (SGOT) ≤ 60 IU/L ALT (SGPT) men ≤ 83 IU/L women < 60 IU/L Alkaline Phosphatase ≤ 200 IU/L Total Bilirubin ≤ 1.2 mg/dL PT and PTT < 1.2 ULN
• Electrocardiogram (ECG) without clinically significant findings as determined by the PI.
• Have adequate renal function as evidenced by the following screening result:
• Glomerular filtration rate (GFR) calculated by Cockcroft-Gault formula >60 ml/min.
• Urinalysis demonstrating < +1 glucose, +1 ketones, and +1 protein.
• Negative pregnancy test within 1 week of study day 1 (women of childbearing potential only).
• Negative urine test for substances of abuse, including opiates, per CRU standards.
• Negative serology tests for HIV, hepatitis B surface antigen, and hepatitis C virus antibody.
• Body Mass Index (BMI) 18.0 to 32 kg/m.
• Cold pressor screening results as follows: 1) pain tolerance of > 20 seconds and <120 seconds.
• Cytochrome P450 2D6 (CYP2D6) genotype by Genelex consistent with intermediate metabolizer phenotype or normal metabolizer phenotype.

You may not qualify if…

• Oral temperature > 38°C or history of current illness.
• History of seizures, epilepsy, or recognized increase risk of seizure (e.g., head trauma, metabolic disorders, alcohol or drug withdrawal).
• History of cirrhosis or laboratory evidence of liver disease.
• Use of alcohol within 24 hours of day -1 until the end of the study; and grapefruit, grapefruit-related citrus fruits (e.g., Seville oranges, pomelos), or grapefruit juice or grapefruit-related juices, or other medication, within 7 days of study drug administration and until the end of the study.
• History of previous anaphylaxis, severe allergic reaction to paroxetine, tramadol, codeine, or other opioid drugs.
• Use of MAO Inhibitors (including linezolid), Serotonin Reuptake Inhibitors, Serotonin-Norepinephrine Reuptake Inhibitors, and prescription or over-the counter (OTC) medications known to induce or inhibit drug metabolism, including CYP2D6, and other drugs that may affect the serotonergic neurotransmitter systems including, but not limited to, triptans, dextromethorphan, tricyclic antidepressants, bupropion, lithium, tramadol, dietary supplements such as tryptophan and St. John's Wort, and antipsychotics or other dopamine antagonists. These restrictions are to be maintained from 14 days before study day -1, until the subject completes the study.
• Any other unstable acute or chronic disease that could interfere with the evaluation of the safety of the study drug as determined by the principal Investigator in dialogue with the Sponsor Medical Monitor.
• Currently pregnant or breast feeding.
• Unlikely to comply with the study protocol.
• Known or suspected alcohol or drug abuse within the past 6 months.
• Received another investigational agent within 4 weeks of Day 1, or receiving any other investigational agent during this study.
• Any concurrent disease or condition that in the opinion of the investigator impairs the subject's ability to complete the trial. Psychological, familial, sociological, geographical or medical conditions which, in the Investigator's opinion, could compromise compliance with the objectives and procedures of this protocol, or obscure interpretation of the trial data.

Where it is running

• PRA Health Sciences — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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