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| ID | Type | Description | Link |
|---|---|---|---|
| C4791001 | Other Identifier | Alias Study Number |
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First In Human (FIH), randomized, double-blind, placebo-controlled single ascending dose (SAD) and multiple ascending dose (MAD) escalation study of approximately 80 subjects. The SAD portion of the study will enroll six cohorts of eight healthy subjects per cohort, for a total of approximately 48 healthy subjects. The MAD portion of the study will enroll four cohorts of eight healthy subjects per cohort, for a total of approximately 32 healthy subjects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort 1 | Experimental | single intravenous dose |
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| Cohort 2 | Experimental | single intravenous dose |
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| Cohort 3 | Experimental | single intravenous dose |
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| Cohort 4 | Experimental | single intravenous dose |
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| Cohort 5 | Experimental | single intravenous dose |
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| Cohort 6 | Experimental | single intravenous dose |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| APX001 single dose 1 | Drug |
| ||
| APX001 single dose 2 |
| Measure | Description | Time Frame |
|---|---|---|
| Safety and tolerability of single and multiple doses of APX001 as measured by adverse events (AEs), physical examinations (PE), vital signs (VS), laboratory safety tests, urinalysis and 12-lead electrocardiograms (ECG). | 21 days |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics of single and multiple doses of APX001 as measured by maximum observed concentration (Cmax). | 21 days | |
| Pharmacokinetics of single and multiple doses of APX001 as measured by area under the curve (AUC). | 21 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Marc Engelhardt | Basilea Pharmaceutica International Ltd, Allschwil | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| PRA Health Sciences | Groningen | 9728 NZ | Netherlands | |||
| PRA Health Sciences |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 36988461 | Result | Hodges MR, Ople E, Wedel P, Shaw KJ, Jakate A, Kramer WG, Marle SV, van Hoogdalem EJ, Tawadrous M. Safety and Pharmacokinetics of Intravenous and Oral Fosmanogepix, a First-in-Class Antifungal Agent, in Healthy Volunteers. Antimicrob Agents Chemother. 2023 Apr 18;67(4):e0162322. doi: 10.1128/aac.01623-22. Epub 2023 Mar 29. |
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| Cohort 7 | Experimental | multiple intravenous doses |
|
| Cohort 8 | Experimental | multiple intravenous doses |
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| Cohort 9 | Experimental | multiple intravenous doses |
|
| Cohort 10 | Experimental | multiple intravenous doses |
|
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| APX001 single dose 3 | Drug |
|
| APX001 single dose 4 | Drug |
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| APX001 single dose 5 | Drug |
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| APX001 single dose 6 | Drug |
|
| APX001 multiple dose 1 | Drug |
|
| APX001 multiple dose 2 | Drug |
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| APX001 multiple dose 3 | Drug |
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| APX001 multiple dose 4 | Drug |
|
| Matching Placebo | Drug |
|
| Pharmacokinetics of single and multiple doses of APX001 as measured by terminal phase half-life (t1/2). | 21 days |
| Pharmacokinetics of single and multiple doses of APX001 as measured by volume of distribution (Vd). | 21 days |
| Pharmacokinetics of single and multiple doses of APX001 as measured by elimination rate constant (Kel). | 21 days |
| Pharmacokinetics of single and multiple dose of APX001 as measured by accumulation ratio. | 21 days |
| Groningen |
| Netherlands |
| ID | Term |
|---|---|
| D009181 | Mycoses |
| ID | Term |
|---|---|
| D001423 | Bacterial Infections and Mycoses |
| D007239 | Infections |
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