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NCT01474798 · ClinicalTrials.gov registry record · Phase 2

Phase II Trial of RA-18C3 in Subjects With Moderate to Severe Acne Vulgaris

A Phase 2 study, sponsored by Janssen Research & Development.

Completed
Registry status
Phase 2
Development phase
11
Enrollment target

NCT01474798: Completed Phase 2 study, sponsored by Janssen Research & Development.

NCT01474798 is a Phase 2 study that has completed, run by Janssen Research & Development. The registered enrollment target is 11 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01474798, a Phase 2 study, has completed, sponsored by Janssen Research & Development.

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target

Study Summary

This is a 91-day phase II, open label trial of the true human monoclonal antibody RA-18C3 in subjects with moderate to severe acne vulgaris. Ten (10) subjects will receive RA-18C3 via subcutaneous injection. Subjects will receive injections at Days 0, 21, and 42 for a total of 3 injections. Study drug will be administered under close observation in a facility equipped to handle medical emergencies. Subjects will not be discharged from the facility until at least 1 hour following the injection or 1 hour after their vital signs have stabilized. Safety will be assessed by pre- and post-treatment serial measurements of vital signs, clinical laboratory assessments, and the recording of adverse clinical events.

Primary Outcome

Incidence and type of adverse clinical events

Interventions

  • DRUG RA-18C3

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2012-02-29
Est. Completion 2012-12-31
Phase Phase 2
Janssen Research & Development

593 total trials

What the finished NCT01474798 record still lists

NCT01474798 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which RA-18C3 is the first listed.

NCT01474798 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01474798 about?

NCT01474798 is a clinical study titled "Phase II Trial of RA-18C3 in Subjects With Moderate to Severe Acne Vulgaris". This is a 91-day phase II, open label trial of the true human monoclonal antibody RA-18C3 in subjects with moderate to severe acne vulgaris. Ten (10) subjects will receive RA-18C3 via subcutaneous injection. Subjects will receive injections at Days 0, 21, and 42 for a total of 3 injections. Study dr...

What is the current status of trial NCT01474798?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2012-02-29. Estimated completion is 2012-12-31.

What interventions are being tested in trial NCT01474798?

The interventions under investigation include: RA-18C3 (DRUG).

Who is sponsoring clinical trial NCT01474798?

This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01474798's enrollment target sits among peer trials

11 1967th of 2000 higher than 33 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01474798, the US trial registry maintained by the National Library of Medicine. NCT01474798 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.