Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01226628 · ClinicalTrials.gov registry record · Phase 1

A Safety Study of CNTO 2476 in Patients With Age-Related Macular Degeneration

A Phase 1 study, sponsored by Janssen Research & Development.

Completed
Registry status
Phase 1
Development phase
39
Enrollment target

NCT01226628: Completed Phase 1 study, sponsored by Janssen Research & Development.

NCT01226628 is a Phase 1 study that has completed, run by Janssen Research & Development. The registered enrollment target is 39 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01226628, a Phase 1 study, has completed, sponsored by Janssen Research & Development.

COMPLETED
Registry status
Phase 1
Development phase
39 participants
Enrollment target

Study Summary

The main purpose of this study to evaluate the safety and tolerability of CNTO 2476 administered subretinally (beneath the retina) using the iTrack Model 275 micro catheter in patients with visual acuity (acuteness or clearness of vision) impairment associated with the geographic atrophy (GA: partial or complete wasting away of retinal layer below the retina) manifestation of age-related macular degeneration (AMD: medical condition which usually affects older adults and results in a loss of vision in the center of the visual field \[the macula\] because of damage to the retina).

Primary Outcome

This number will be summarized descriptively for treated and fellow eyes within each dose level included in Phase 1 and Phase 2a portions of the study

Interventions

  • BIOLOGICAL CNTO 2476
  • PROCEDURE iTrack Model 275 micro catheter

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2010-10-21
Est. Completion 2017-05-31
Phase Phase 1
Janssen Research & Development

593 total trials

What the finished NCT01226628 record still lists

NCT01226628 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower).

The record links to 0 conditions, and to 2 interventions - of which CNTO 2476 is the first listed.

NCT01226628 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01226628 about?

NCT01226628 is a clinical study titled "A Safety Study of CNTO 2476 in Patients With Age-Related Macular Degeneration". The main purpose of this study to evaluate the safety and tolerability of CNTO 2476 administered subretinally (beneath the retina) using the iTrack Model 275 micro catheter in patients with visual acuity (acuteness or clearness of vision) impairment associated with the geographic atrophy (GA: partia...

What is the current status of trial NCT01226628?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2010-10-21. Estimated completion is 2017-05-31.

What interventions are being tested in trial NCT01226628?

The interventions under investigation include: CNTO 2476 (BIOLOGICAL), iTrack Model 275 micro catheter (PROCEDURE).

Who is sponsoring clinical trial NCT01226628?

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 NCT01226628's enrollment target sits among peer trials

39 1191st of 2000 higher than 804 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03465592 · 39 participants · Phase 1

    Trial of Nivolumab Following Partially Human Leukocyte Antigen (HLA) Mismatched BMT in Children & Adults With Sarcoma

  • NCT03961776 · 39 participants

    Monitoring Treatment Response With On-board DWI During Neo-adjuvant Chemo-radiation for Rectal Cancer Using Magnetic Resonance-guided-radiotherapy Systems

  • NCT04050280 · 39 participants · Phase 2

    CLAG-GO for Patients With Persistent, Relapsed or Refractory AML

  • NCT04190862 · 39 participants · Phase 1

    E-CEL UVEC as an Adjunct Cell Therapy for Treatment of Anal Fistulas

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01226628, the US trial registry maintained by the National Library of Medicine. NCT01226628 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.