Study to Assess the Bioavailability, Pharmacokinetics, Safety, and Tolerability of AVP-923 in Healthy Adult Participants
Completed · Phase 1
Conditions studied: Healthy Adult Male and Female Volunteers
In brief
This study will be conducted to evaluate the relative bioavailability, pharmacokinetics, safety, and tolerability of AVP-923 (dextromethorphan hydrobromide \[DM\] and quinidine sulfate \[Q\] capsules) when the contents of a capsule are administered in applesauce or via a nasogastric feeding tube, compared with administration of a capsule in healthy, fasting, adult participants.
Key facts
- Study ID
- NCT03381664
- Run by
- Avanir Pharmaceuticals
- People needed
- 17
- Starts
- 2017-11-28
- Expected to finish
- 2018-01-30
- Last updated by the study team
- 2018-02-23
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy adults, 18 to 65 years of age, inclusive
- Willing to sign informed consent form
- Cytochrome P450 2D6 genotype that confers extensive metabolizer profile (as per documented phenotype interpretation from local laboratory and approval from Avanir)
You may not qualify if…
- History or presence of significant pulmonary, hepatic, renal, hematologic, allergic, endocrine (including diabetes), immunologic, dermatologic, neurologic (including history or presence of seizures or convulsive disorders), psychiatric disease (including history of suicidal ideation or behavior) or any eating disorder deemed clinically significant by the investigator
- History or presence of significant cardiovascular disease, including complete heart block, QT interval corrected for heart rate (QTc) prolongation, and/or torsades de pointes
- History or presence of any gastrointestinal (GI) disease or condition that could compromise participant safety or affect the absorption of study drug, including GI ulcers, GI bleeding, esophageal or gastric varices, and dyspepsia requiring regular (i.e., more frequently than once a month) use of acid-reducing drugs
- Known hypersensitivity/intolerance to dextromethorphan or quinidine
- Participants whom the principal investigator or his delegate deems to be ineligible
Where it is running
- Vince & Associates Clinical Research — Overland Park, Kansas, United States
Full record on ClinicalTrials.gov
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