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Active, not recruiting Phase 2 Interventional

Phase 2 Tolerability and Effects of ALK-001 on Stargardt Disease

ClinicalTrials.gov ID: NCT02402660

Public ClinicalTrials.gov record NCT02402660. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 10:38 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Multicenter, Double-Masked, Randomized, Placebo-Controlled Study to Investigate the Long Term Safety, Tolerability, Pharmacokinetics and Effects of ALK-001 on the Progression of Stargardt Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the long term safety and tolerability of ALK-001 (C20-D3-retinyl acetate), and to explore the effects of ALK-001 on the progression of Stargardt disease in patients between the ages of 8 and 70 years old. Funding Source - FDA OOPD

Study identification

NCT ID
NCT02402660
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alkeus Pharmaceuticals, Inc.
Industry
Enrollment
160 participants

Conditions and interventions

Eligibility (public fields only)

Age range
8 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2015 (Actual)
Primary completion
Jun 30, 2028 (Estimated)
Completion
Nov 30, 2028 (Estimated)
Last update posted
Sep 21, 2026

2015 – 2028

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Alkeus Site Phoenix Arizona 85020 —
Alkeus Site Los Angeles California 90095 —
Alkeus Site Aurora Colorado 80045 —
Alkeus Site Gainesville Florida 32601 —
Alkeus Site Miami Florida 33136 —
Alkeus Site Indianapolis Indiana 46202 —
Alkeus Site Baltimore Maryland 21287 —
Alkeus Site Grand Rapids Michigan 49546 —
Alkeus Site New York New York 10032 —
Alkeus Site Westbury New York 11590 —
Alkeus Site Houston Texas 77025 —
Alkeus Site Salt Lake City Utah 84132 —
Alkeus Site Silverdale Washington 98383 —
Alkeus Site Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02402660, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 21, 2026 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02402660 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →