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The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics of escalating multiple oral doses of varenicline AMT 8 controlled release formulation for 14 days in adult smokers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort 1 | Other | Subjects will be randomized to receive either experimental drug (N=9) or matching placebo (N=3). |
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| Cohort 2 | Other | Subjects will be randomized to receive either experimental drug (N=9) or matching placebo (N=3). |
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| Cohort 3 | Other | Subjects will be randomized to receive either experimental drug (N=9) or matching placebo (N=3). |
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| Optional Cohort 4 | Other | Subjects will be randomized to receive either experimental drug (N=9) or matching placebo (N=3). |
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| Optional Cohort 5 | Other | Subjects will be randomized to receive either experimental drug (N=9) or matching placebo (N=3). |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Varenicline Tartrate | Drug | Varenicline 1.8 mg AMT-8 controlled release tablets administered twice a day for 14 days. |
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| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetic endpoints include varenicline area under the curve from 0-24 hours (AUC24), maximum plasma concentration (Cmax), | Day 1 and Day 14 | |
| Safety endpoints include evaluation of clinical safety laboratory tests, supine vital signs, triplicate 12-lead ECGs and adverse events. | up to 14 days | |
| Time of maximum plasma concentration (Tmax) on Day 1 and Day 14 | Day 1 and Day 14 | |
| Minimum plasma concentration (Cmin), terminal half life (t1/2), observed accumulation ratio (Rac), peak:trough fluctuation (%PTF) on Day 14 only. | Day 14 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Pfizer CT.gov Call Center | Pfizer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pfizer Investigational Site | East Grand Forks | Minnesota | 58721 | United States | ||
| Pfizer Investigational Site |
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| Label | URL |
|---|---|
| To obtain contact information for a study center near you, click here. | View source |
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| ID | Term |
|---|---|
| D016540 | Smoking Cessation |
| ID | Term |
|---|---|
| D015438 | Health Behavior |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| D000068580 | Varenicline |
| ID | Term |
|---|---|
| D001552 | Benzazepines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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| Varenicline Tartrate | Drug | Planned dose is Varenicline 2.4 mg AMT-8 controlled release tablets administered twice a day for 14 days. Actual dose may be adjusted based on emerging data from prior dose cohorts. |
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| Varenicline Tartrate | Drug | Planned dose is Varenicline 3 mg AMT-8 controlled release tablets administered twice a day for 14 days. Actual dose may be adjusted based on emerging data from prior dose cohorts. |
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| Varenicline Tartrate | Drug | The dose to be administered is not yet determined and will be based on emerging data from prior dose cohorts. The dose will be administered as Varenicline AMT-8 controlled release tablets twice a day for 14 days. The doses to be tested may be lower, higher or repeat a previously tested dose and may include a titration. |
|
| Varenicline Tartrate | Drug | The dose to be administered is not yet determined and will be based on emerging data from prior dose cohorts. The dose will be administered as Varenicline AMT-8 controlled release tablets twice a day for 14 days. The doses to be tested may be lower, higher or repeat a previously tested dose and may include a titration. |
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| Fargo |
| North Dakota |
| 58104 |
| United States |
| D011810 | Quinoxalines |