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| ID | Type | Description | Link |
|---|---|---|---|
| 2024-518535-11-00 | Registry Identifier | CTIS (EU) |
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The purpose of this study is to learn about how much the study medicine PF-07976016 will be taken up and processed by healthy male participants. The total number of weeks of the study is up to approximately 12 weeks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm 1 | Experimental | Participants will receive doses of PF-07976016 with and without radiolabel. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| [14C] PF-07976016 | Drug | [14C] PF-07976016 liquid (oral) formulation |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Total recovery of radioactivity expressed as a percent of total oral radioactive dose administered. | From dose (Day 1) and for up to 21 days thereafter |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with treatment emergent adverse events | First dose (Day 1) through 28 to 35 days after final dose (approximately 12 weeks) |
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Inclusion Criteria:
Exclusion Criteria:
Healthy male participants
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| Name | Affiliation | Role |
|---|---|---|
| Pfizer CT.gov Call Center | Pfizer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| ICON | Groningen | 9728 NZ | Netherlands |
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| Label | URL |
|---|---|
| To obtain contact information for a study center near you, click here. | View source |
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Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.
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| PF-07976016 |
| Drug |
PF-07976016 liquid (oral) formulation |
|
| [14C] PF-07976016 | Drug | [14C] PF-07976016 intravenous (IV) formulation |
|