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A study to evaluate the pharmacokinetics and bioequivalence of sumatriptan delivered by the Intraject system.
A single center, randomized, single-dose, open-label, partial-block, four-period, four-way crossover study in 54 healthy adult subjects to evaluate the pharmacokinetics and bioequivalence of sumatriptan delivered by the Intraject system compared to IMITREX STATdose at three injection sites (abdomen, thigh, and arm.)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| A | Experimental | IMITREX -abd. to Intraject-abd. to IMITREX -thigh to Intraject-thigh |
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| B | Experimental | Intraject-abd. to IMITREX -abd. to Intraject-thigh to IMITREX -thigh |
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| C | Experimental | Intraject-abd to IMITREX -abd to Intraject-arm. to IMITREX -arm. |
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| D | Experimental | IMITREX-abd to Intraject-abd to IMITREX-arm. to Intraject-arm. |
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| E | Experimental | IMITREX-arm to Intraject-arm to IMITREX-thigh to Intraject-thigh |
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| F | Experimental | Intraject-thigh to IMITREX-thigh to Intraject-arm to IMITREX-arm |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Sumatriptan (via Intraject System) | Device | 0.5 mL of solution with 6 mg of sumatriptan (base) as the succinate salt |
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| Measure | Description | Time Frame |
|---|---|---|
| The area under the plasma concentration-time curve, maximal plasma concentration, time to maximal concentration, terminal elimination half-life, and apparent terminal elimination rate constant of sumatriptan will be determined at each of 3 sites | one week |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Patricia Chandler, MD | Covance | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Covance, Inc | Dallas | Texas | 75247 | United States |
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