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Comparing the Extent to Which Two Evolocumab Drug Products Are Made Available in the Body After a Single Subcutaneous Dose
NCT07422285 · View on ClinicalTrials.gov ↗
Study Summary
The main objective of this trial is to evaluate the pharmacokinetics of two evolocumab drug products in healthy participants.
Conditions Studied
Interventions
- DRUG Evolocumab Drug Substance A
- DRUG Evolocumab Drug Substance B
Study Locations (4)
Florida
- Fortrea Clinical Research Unit - Daytona Beach — Daytona Beach
Missouri
- QPS Bio-Kinetic — Springfield
Texas
- Fortrea Clinical Research Unit - Dallas — Dallas
Wisconsin
- Fortrea Clinical Research Unit Inc. - Madison — Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2026-01-16 |
| Est. Completion | 2026-07-07 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07422285
The ClinicalTrials.gov registry entry for NCT07422285 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 266 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Healthy Participants appearing as the primary indexed condition, and to 2 interventions — of which Evolocumab Drug Substance A is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07422285 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Florida, Missouri, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07422285 about?
NCT07422285 is a clinical study titled "Comparing the Extent to Which Two Evolocumab Drug Products Are Made Available in the Body After a Single Subcutaneous Dose". The main objective of this trial is to evaluate the pharmacokinetics of two evolocumab drug products in healthy participants.
What is the current status of trial NCT07422285?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 400 participants. The study started on 2026-01-16. Estimated completion is 2026-07-07.
What conditions does trial NCT07422285 study?
This clinical trial studies the following conditions: Healthy Participants, Pharmacokinetics. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07422285?
The interventions under investigation include: Evolocumab Drug Substance A (DRUG), Evolocumab Drug Substance B (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07422285?
This trial is sponsored by Amgen, which has 266 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07422285 being conducted?
This trial has 4 study locations across Florida, Missouri, Texas, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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