230 Participants NeededMy employer runs this trial

ALK-001 for Stargardt Disease

(NORTHSTAR Trial)

Recruiting at 13 trial locations
Ft
Overseen ByFor trial questions: trials@alkeuspharma.com or 877-255-7476
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new drug called ALK-001 to determine its effectiveness for people with Stargardt disease, a genetic eye condition that affects vision. The study aims to evaluate the drug's efficacy and safety for patients. Participants are divided into two groups: one receives ALK-001, and the other receives a placebo (a substance with no therapeutic effect). Suitable candidates include those diagnosed with Stargardt disease and possessing a genetic report confirming the condition. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants an opportunity to contribute to a potentially groundbreaking treatment.

Will I have to stop taking my current medications?

The trial does not specify if you need to stop taking your current medications, but you cannot take supplements with vitamin A or beta-carotene, liver-based products, or certain prescription medications within 30 days before starting the trial.

Is there any evidence suggesting that ALK-001 is likely to be safe for humans?

In earlier studies, ALK-001 showed promising safety results for people with Stargardt disease. Research indicates that this treatment is generally well-tolerated, with no serious side effects reported. ALK-001, a modified form of vitamin A, is designed for greater efficiency. It has undergone several trials and demonstrated safety for use. In one study, it slowed the progression of eye damage, indicating potential effectiveness. Overall, the safety data appears positive, confirming the treatment's safety for humans in these earlier trials.12345

Why do researchers think this study treatment might be promising for Stargardt disease?

Most treatments for Stargardt Disease focus on managing symptoms and slowing progression, but ALK-001 offers a promising new approach. Unlike existing options, ALK-001 is designed to slow down the accumulation of toxic vitamin A byproducts in the retina, which are a key cause of vision loss in this condition. This mechanism of action is particularly exciting because it targets the root cause rather than just the symptoms, potentially offering a more effective way to preserve vision. Researchers are hopeful that this could significantly improve the quality of life for those affected by Stargardt Disease.

What evidence suggests that ALK-001 might be an effective treatment for Stargardt disease?

Research has shown that ALK-001, also known as gildeuretinol, may help treat Stargardt disease. Studies have found that ALK-001 can slow the disease's progression and, in some cases, even halt its worsening for up to six years. ALK-001 works by preventing certain changes in vitamin A, which are believed to contribute to Stargardt disease. Other research has found that it can also slow the growth of damaged areas in the retina, known as geographic atrophy (GA) lesions. In this trial, participants will receive either ALK-001 or a placebo. Overall, ALK-001 appears to be a well-tolerated treatment with positive effects on slowing the disease.15678

Are You a Good Fit for This Trial?

This trial is for males and females aged 8 to 45 with a confirmed genetic diagnosis of Stargardt disease. Participants must not be pregnant or breastfeeding, must avoid certain supplements and medications, and cannot have recently joined other drug or device studies.

Inclusion Criteria

Have signed and dated the informed consent forms (ICFs; or assent as appropriate) to participate
I am willing to use birth control as required during and after the study.
I have been diagnosed with typical autosomal recessive Stargardt macular dystrophy.
See 2 more

Exclusion Criteria

I have not taken vitamin A, beta-carotene, liver products, or oral retinoids recently.
I am pregnant, breastfeeding, or planning to have a child during the study.
I have not had gene, cell, or device therapy for STGD, and no drug study in the past 6 months.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive ALK-001 or placebo to evaluate efficacy and safety in Stargardt disease

24 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • ALK-001

Trial Overview

The study compares ALK-001, an investigational drug, to a placebo in people with Stargardt disease. Participants are randomly assigned to receive either ALK-001 or the placebo to see if the drug can slow down vision loss.

How Is the Trial Designed?

2

Treatment groups

Active Control

Placebo Group

Group I: ActiveActive Control1 Intervention
Group II: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Alkeus Pharmaceuticals, Inc.

Lead Sponsor

Trials
4
Recruited
520+

Citations

Study of ALK-001 on the Progression of Stargardt Disease

It identifies the role of the intervention that participants receive. Types of arms include experimental arm, active comparator arm, placebo comparator arm, ...

October 9, 2025

Results from the study of oral gildeuretinol in moderate Stargardt disease to be presented as late-breaker during Retina Subspecialty Day.

Stargardt disease ALK-001 phase 2 clinical trial - IOVS

The primary endpoint is safety of two dose levels of ALK-001, while efficacy outcomes include atrophy lesion size by fundus autofluorescence (FAF), best- ...

Study of ALK-001 on the Progression of Stargardt Disease

This study evaluates the efficacy and safety of investigational study drug ALK-001 in participants 8 to 45 years of age, inclusive, ...

TEASE-3 study: Positive interim data are reported for ...

The TEASE-3 study of gildeuretinol (ALK-001) which showed that treatment halted progression of early-stage Stargardt disease for up to 6 years.

Phase 1 Safety Study of ALK-001 in Healthy Volunteers

This protocol is a phase 1 clinical study to assess the safety and pharmacokinetics of ALK-001 in healthy volunteers.

Favorable safety data supports Alkeus' oral gildeuretinol for ...

Alkeus receives two rare disease FDA designations for Stargardt candidate ... ALK-001 demonstrated both “safety and tolerability,” with no ...

Alkeus Pharmaceuticals Presents Gildeuretinol Data ...

The study showed daily oral gildeuretinol significantly slowed the growth of atrophic retinal lesions in Stargardt disease by a 21.6% reduction versus the ...