Phase 2
Completed N=5
PK/PD Comparison of Guanfacine ER and IR
Source: ClinicalTrials.gov NCT01904526 ↗Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Apr 2018
Primary outcomePrimary: Plasma Trough Levels of Guanfacine — 3.40; 3.46; 5.92 ng/ml
Summary
Evaluate whether a 4mg/day or 6/mg day dose of extended-release guanfacine produces pharmacokinetic/dynamic (PK/PD) properties similar to 3mg/day immediate release guanfacine.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Plasma Trough Levels of Guanfacine |
3.40; 3.46; 5.92 | — |
| SECONDARY Heart Rate |
59.6; 58.8; 61.6 | — |
| SECONDARY Systolic Blood Pressure |
101.0; 107.4; 108.4 | — |
Eligibility Criteria
Inclusion Criteria
- Age 18-65
- Able to read, write and comprehend English
- Smoker
- Able to take oral medications and willing to adhere to medication regimen
- Provide evidence of a stable living residence in the last 2 months, have reasonable transportation to the study site, and have no plans to move within the next 3 months or unresolved legal problems.
Exclusion Criteria
- Any significant current medical conditions that would contraindicate smoking
- Current Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) abuse or dependence of other substances, other than nicotine dependence or alcohol abuse
- Positive test results at intake appointment on urine drug screens for illicit drugs
- Past 30 day use of psychoactive drugs including anxiolytics and antidepressants
- Women who are pregnant or nursing
- Suicidal, homicidal or evidence of current mental illness such as schizophrenia, bipolar disorder or major depression, or anxiety disorders
- Meeting DSM-IV criteria for current attention deficit hyperactivity disorder (ADHD)
- Individuals who are currently taking medications known to be effective for smoking cessation or are regular users of other tobacco products in the past 30 days
- Only one member per household can participate in the study
- Specific exclusions for administration of guanfacine not already specified include:
- EKG evidence at baseline screening of any clinically significant conduction abnormalities or arrhythmias
- Known intolerance for guanfacine or any alpha blocker
- History of fainting, syncopal attacks
- Heart failure or myocardial infarction
- Impaired liver (as indicated by aspartate aminotransferase (AST), alanine aminotransferase (ALT) >3x normal)
- Renal function (as indicated by estimated creatinine clearance <60cc/min)
- Treatment with any antihypertensive drug or any alpha-adrenergic blocker
- Use of any central nervous system depressant (e.g., phenothiazines, barbiturates, benzodiazepines)
- Use of strong cytochrome P450 3A4 (CYP3A4) inhibitors (e.g., ketoconazole) or inducers (e.g., rifampin), or consumption of grapefruit juice
- Subjects may have not donated blood in the past 8 weeks or have been involved in other investigational studies that involve substantial blood draws or medications unknown to us
Data sourced from ClinicalTrials.gov (NCT01904526). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.