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ACTIVE NOT RECRUITING Phase 2

Phase I/II Follow-up Study of SAR422459 in Patients With Stargardt's Macular Degeneration

NCT01736592 · View on ClinicalTrials.gov ↗

Study Summary

Primary Objective: To evaluate the long-term safety and tolerability of SAR422459 in patients with Stargardt's Macular Degeneration. Secondary Objective: To assess: * Safety * Biological activity

Conditions Studied

Interventions

  • DRUG Long term follow up in all patients who received SAR422459 in previous study TDU13583

Study Locations (2)

Oregon

  • Oregon Health and Science University Site Number : 840001 — Portland

Other

  • Investigational Site Number : 250001 — Paris

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2012-12-14
Est. Completion 2033-08-29
Phase Phase 2

Sponsor

Sanofi

275 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01736592

The ClinicalTrials.gov registry entry for NCT01736592 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sanofi, which has 275 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 Stargardt's Disease appearing as the primary indexed condition, and to 1 intervention — of which Long term follow up in all patients who received SAR422459 in previous study TDU13583 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: NCT01736592 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Oregon, Other. 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 NCT01736592 about?

NCT01736592 is a clinical study titled "Phase I/II Follow-up Study of SAR422459 in Patients With Stargardt's Macular Degeneration". Primary Objective: To evaluate the long-term safety and tolerability of SAR422459 in patients with Stargardt's Macular Degeneration. Secondary Objective: To assess: * Safety * Biological activity

What is the current status of trial NCT01736592?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 27 participants. The study started on 2012-12-14. Estimated completion is 2033-08-29.

What conditions does trial NCT01736592 study?

This clinical trial studies the following conditions: Stargardt's Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01736592?

The interventions under investigation include: Long term follow up in all patients who received SAR422459 in previous study TDU13583 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01736592?

This trial is sponsored by Sanofi, which has 275 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01736592 being conducted?

This trial has 2 study locations across Oregon. 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