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NCT06393517 · ClinicalTrials.gov registry record · Phase 1
A Study to Learn How Different Forms of the Study Medicine Called PF-06954522 Are Taken up Into the Blood in Healthy Adults
A Phase 1 study, sponsored by Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 23
- Enrollment target
NCT06393517: Completed Phase 1 study, sponsored by Pfizer.
NCT06393517 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 23 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06393517, a Phase 1 study, has completed, sponsored by Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 23 participants
- Enrollment target
Study Summary
The purpose of this study is to compare three finished products of PF-06954522 in terms of the uptake into the blood stream. This study is seeking participants who are: \- Healthy male or female participants aged 18 years or older. All participants in this study will receive PF-06954522 once by mouth. The participants may receive different tablets by mouth for PF-06954522. The study will compare experiences of people receiving three different products of PF-06954522. This will help understand how much PF-06954522 is taken up into the blood for each product given. Participants will take part into the study for about 77 days. During this time participants will have to stay onsite for 21 days. There will be one follow up (by telephone) study visit.
Interventions
- DRUG PF-06954522 IR (Formulation 1)
- DRUG PF-06954522 MR (Formulation 2)
- DRUG PF-06954522 MR (Formulation 3)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2024-04-30 |
| Est. Completion | 2024-09-01 |
| Phase | Phase 1 |
What the finished NCT06393517 record still lists
NCT06393517 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower).
The record links to 0 conditions, and to 3 interventions - of which PF-06954522 IR (Formulation 1) is the first listed.
NCT06393517 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06393517 about?
NCT06393517 is a clinical study titled "A Study to Learn How Different Forms of the Study Medicine Called PF-06954522 Are Taken up Into the Blood in Healthy Adults". The purpose of this study is to compare three finished products of PF-06954522 in terms of the uptake into the blood stream. This study is seeking participants who are: \- Healthy male or female participants aged 18 years or older. All participants in this study will receive PF-06954522 once by m...
What is the current status of trial NCT06393517?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2024-04-30. Estimated completion is 2024-09-01.
What interventions are being tested in trial NCT06393517?
The interventions under investigation include: PF-06954522 IR (Formulation 1) (DRUG), PF-06954522 MR (Formulation 2) (DRUG), PF-06954522 MR (Formulation 3) (DRUG).
Who is sponsoring clinical trial NCT06393517?
This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06393517's enrollment target sits among peer trials
23 1596th of 2000 higher than 400 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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