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NCT06438263 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate Bioavailability of Rocatinlimab Autoinjector and Vial in Healthy Participants

A Phase 1 study, sponsored by Amgen.

Completed
Registry status
Phase 1
Development phase
231
Enrollment target

NCT06438263: Completed Phase 1 study, sponsored by Amgen.

NCT06438263 is a Phase 1 study that has completed, run by Amgen. The registered enrollment target is 231 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (285% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06438263, a Phase 1 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 1
Development phase
231 participants
Enrollment target

Study Summary

The main objective of this study is to evaluate the pharmacokinetics (PK) of rocatinlimab given as a single subcutaneous (SC) autoinjector dose compared to vial in healthy participants.

Interventions

  • DRUG Rocatinlimab

Trial Details

FieldValue
Enrollment Target 231 participants
Start Date 2024-08-06
Est. Completion 2025-07-02
Phase Phase 1
Amgen

558 total trials

What the finished NCT06438263 record still lists

NCT06438263 is an interventional study that assigns participants to a tested intervention. The registered 231 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (285% higher).

The record links to 0 conditions, and to 1 intervention - of which Rocatinlimab is the first listed.

NCT06438263 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06438263 about?

NCT06438263 is a clinical study titled "A Study to Evaluate Bioavailability of Rocatinlimab Autoinjector and Vial in Healthy Participants". The main objective of this study is to evaluate the pharmacokinetics (PK) of rocatinlimab given as a single subcutaneous (SC) autoinjector dose compared to vial in healthy participants.

What is the current status of trial NCT06438263?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 231 participants. The study started on 2024-08-06. Estimated completion is 2025-07-02.

What interventions are being tested in trial NCT06438263?

The interventions under investigation include: Rocatinlimab (DRUG).

Who is sponsoring clinical trial NCT06438263?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06438263's enrollment target sits among peer trials

231 217th of 2000 higher than 1,782 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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Source: ClinicalTrials.gov NCT06438263, the US trial registry maintained by the National Library of Medicine. NCT06438263 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.