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COMPLETED Phase 1

RBM-007 in Subjects witH ExudatIve Age-related Macular Degeneration

NCT03633084 · View on ClinicalTrials.gov ↗

Study Summary

This is an open label, non-controlled, dose-escalating study assessing the safety, tolerability, and bioactivity of a single intravitreal (i.vt.) injection of RBM-007 in approximately nine subjects with exudative age-related macular degeneration.

Interventions

  • DRUG RBM-007 Injectable Solution

Study Locations (4)

California

  • Retinal Consultants Medical Group — Sacramento
  • Retinal Consultants Medical Group — Sacramento
  • Stanford University — Stanford
  • Bay Area Retina Associates — Walnut Creek

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2018-08-29
Est. Completion 2019-06-26
Phase Phase 1

Sponsor

Ribomic USA

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03633084

The ClinicalTrials.gov registry entry for NCT03633084 describes a study currently listed as completed. 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 9 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ribomic USA, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Age-related Macular Degeneration appearing as the primary indexed condition, and to 1 intervention — of which RBM-007 Injectable Solution 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: NCT03633084 reports 4 study locations spanning 1 distinct geographic area — top geographies include California. 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 NCT03633084 about?

NCT03633084 is a clinical study titled "RBM-007 in Subjects witH ExudatIve Age-related Macular Degeneration". This is an open label, non-controlled, dose-escalating study assessing the safety, tolerability, and bioactivity of a single intravitreal (i.vt.) injection of RBM-007 in approximately nine subjects with exudative age-related macular degeneration.

What is the current status of trial NCT03633084?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 9 participants. The study started on 2018-08-29. Estimated completion is 2019-06-26.

What conditions does trial NCT03633084 study?

This clinical trial studies the following conditions: Age-related Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03633084?

The interventions under investigation include: RBM-007 Injectable Solution (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03633084?

This trial is sponsored by Ribomic USA, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03633084 being conducted?

This trial has 4 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial