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The purpose of this study is to assess the safety, tolerability and pharmacokinetics of single and multiple doses of XPF-001 in healthy volunteers.
The effect of food on the pharmacokinetics of XPF-001 will also be studied.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort 1: Single dose of XPF-001 | Experimental |
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| Cohort 2: Single dose of XPF-001 | Experimental |
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| Cohort 3: Single dose of XPF-001 | Experimental |
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| Cohort 4: Single dose of XPF-001 | Experimental |
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| Cohort 5: Single dose of XPF-001 | Experimental |
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| Cohort A: Repeated doses of XPF-001 | Experimental |
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| Cohort B: Repeated doses of XPF-001 | Experimental |
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| Cohort C: Repeated doses of XPF-001 |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| XPF-001 | Drug | Single oral dose, or 6 days of repeated oral doses. |
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| Measure | Description | Time Frame |
|---|---|---|
| ECGs, Telemetry, Vital Signs, Physical Examinations, Laboratory Assessments and Adverse Events. | up to 14 days post dose |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Richard Larouche, MD | Anapharm | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Anapharm | Montreal | Quebec | Canada |
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| Experimental |
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