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NCT06531811 · ClinicalTrials.gov registry record · Phase 1
A Study to Investigate the Relative Bioavailability of AZD8630 Following a Device and Formulation Transition in Healthy Participants.
A Phase 1 study of Healthy Participants, sponsored by AstraZeneca.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
- 1
- Study location
NCT06531811 is a Phase 1 study of Healthy Participants that has completed, run by AstraZeneca. The registered enrollment target is 32 participants, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (51% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06531811, a Phase 1 study of Healthy Participants, has completed, sponsored by AstraZeneca.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate the potential difference between pharmacokinetics (PK), safety, tolerability and device performance between the AZD8630 test formulation and the AZD8630 reference formulation.
Conditions Studied
Interventions
- DRUG AZD8630 (test formulation) via test inhaler
- DRUG AZD8630 (reference formulation) via Monodose inhaler
- DEVICE Test inhaler
- DEVICE Monodose inhaler
Study Locations (1)
Maryland
- Research Site - Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2024-08-06 |
| Est. Completion | 2024-10-03 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06531811
The ClinicalTrials.gov registry entry for NCT06531811 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (51% lower). The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 4 interventions - of which AZD8630 (test formulation) via test inhaler is the first listed.
NCT06531811 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT06531811 about?
NCT06531811 is a clinical study titled "A Study to Investigate the Relative Bioavailability of AZD8630 Following a Device and Formulation Transition in Healthy Participants.". The purpose of this study is to evaluate the potential difference between pharmacokinetics (PK), safety, tolerability and device performance between the AZD8630 test formulation and the AZD8630 reference formulation.
What is the current status of trial NCT06531811?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2024-08-06. Estimated completion is 2024-10-03.
What conditions does trial NCT06531811 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT06531811?
The interventions under investigation include: AZD8630 (test formulation) via test inhaler (DRUG), AZD8630 (reference formulation) via Monodose inhaler (DRUG), Test inhaler (DEVICE), Monodose inhaler (DEVICE).
Who is sponsoring clinical trial NCT06531811?
This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06531811 being conducted?
This trial has 1 study location across Maryland. 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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