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NCT06301971 · ClinicalTrials.gov registry record · Phase 1
A Study to Assess Mass Balance, Pharmacokinetics, Metabolism, and Excretion of Emraclidine in Healthy Adult Male Participants
A Phase 1 study of Healthy Participants, sponsored by Cerevel Therapeutics.
- Completed
- Registry status
- Phase 1
- Development phase
- 8
- Enrollment target
- 1
- Study location
NCT06301971 is a Phase 1 study of Healthy Participants that has completed, run by Cerevel Therapeutics. The registered enrollment target is 8 participants, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06301971, a Phase 1 study of Healthy Participants, has completed, sponsored by Cerevel Therapeutics.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 8 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary purpose of this study is to determine the mass balance, routes, and rates of elimination of total radioactivity and characterize the pharmacokinetics (PK) of emraclidine, metabolite CV-0000364, and total radioactivity in plasma and whole blood following a single oral dose of \[14C\]-emraclidine in healthy adult male participants.
Conditions Studied
Interventions
- DRUG Emraclidine
Study Locations (1)
Texas
- Austin, Texas - Austin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2024-03-04 |
| Est. Completion | 2024-04-04 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06301971
The ClinicalTrials.gov registry entry for NCT06301971 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (88% lower). The listed sponsor is Cerevel Therapeutics, which has 21 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 1 intervention - of which Emraclidine is the first listed.
NCT06301971 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06301971 about?
NCT06301971 is a clinical study titled "A Study to Assess Mass Balance, Pharmacokinetics, Metabolism, and Excretion of Emraclidine in Healthy Adult Male Participants". The primary purpose of this study is to determine the mass balance, routes, and rates of elimination of total radioactivity and characterize the pharmacokinetics (PK) of emraclidine, metabolite CV-0000364, and total radioactivity in plasma and whole blood following a single oral dose of \[14C\]-emra...
What is the current status of trial NCT06301971?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2024-03-04. Estimated completion is 2024-04-04.
What conditions does trial NCT06301971 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT06301971?
The interventions under investigation include: Emraclidine (DRUG).
Who is sponsoring clinical trial NCT06301971?
This trial is sponsored by Cerevel Therapeutics, which has 21 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06301971 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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