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To compare the bioavailability and pharmacokinetic profiles of two different formulations MN-166 50mg, extended release (ER) tablets with MN-166 10mg capsules in a single-dose regimen in healthy volunteers
Part 1:
To compare the bioavailability and pharmacokinetic profiles of two different formulations MN-166 50mg, extended release (ER) tablets with MN-166 10mg capsules in a single-dose regimen in healthy volunteers; and To choose one of the two MN-166 50mg ER tablet formulations for evaluation in Part 2.
Secondary: To determine the safety and tolerability of the two formulations of MN-166 ER tablets in a single-dose regimen in healthy volunteers.
Part 2:
To compare the bioavailability and steady-state pharmacokinetic profile of MN-166 50mg ER tablet with MN-166 10mg capsules in a multiple-dose regimen in healthy volunteers; and
Secondary: To determine the safety and tolerability of MN-166 ER tablets in a multiple-dose regimen in healthy volunteers
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Extended-release formulation 1 (ER1) | Experimental | 50mg MN-166 tablet. This formulation is intended for once-a-day dosing, hence, the label of extended-release. |
|
| Extended-release formulation 2 (ER2) | Experimental | 50mg MN-166 tablet. This formulation is intended for once-a-day dosing, hence, the label of extended-release. |
|
| Intermediate-release formulation (IR) | Active Comparator | 10mg MN-166 capsule. This formulation is typically given two or three times daily, hence, the label of intermediate-release. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MN-166 | Drug | an orally available small molecule drug approved in Japan and Korea for asthma and post-stroke complications and has been prescribed for these indications for more than 25 years |
| Measure | Description | Time Frame |
|---|---|---|
| Compare the PK Profile of two new formulations in Single-day dose of MN-166 | Compare the maximum plasma concentrations [Cmax] of MN-166 of two different formulations MN-166 50mg, extended release (ER) tablets with MN-166 10mg capsules in a single-dose regimen in healthy volunteers. | 5 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Compare the incidence of treatment-emergent adverse events of two new formulations in Single-day dose of MN-166 | Compare the number and frequency of treatment-emergent adverse events (serious and non-serious) profiles of two different formulations MN-166 50mg, extended release (ER) tablets with MN-166 10mg capsules in a single-dose regimen in healthy volunteers. | 5 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Robina Smith, MD | WCCT Global, Inc. | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| WCCT Global, Inc. | Cypress | California | 90630 | United States |
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| ID | Term |
|---|---|
| C038366 | ibudilast |
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Subjects will receive the following three treatments in a crossover fashion, administered one week apart:
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| Compare the PK Profile of two new formulations in Multi-day dose of MN-166 | Compare the maximum plasma concentrations [Cmax] of MN-166 of two different formula in a multiple-dose regimen. | 3 weeks |
| Compare the incidence of treatment-emergent adverse events of two new formulations in Multi-day dose of MN-166 | Compare the number and frequency of treatment-emergent adverse events (serious and non-serious) of MN-166 (pharmacokinetic profiles) of two different formula in a multiple-dose regimen. | 3 weeks |