The Natural History of the Progression of Atrophy Secondary to Stargardt Disease Type 4: PROM1-Related Macular Dystrophy

Stargardt Disease Clinical Trial

— ProgStar-4  

Official title:

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease Type 4 (STGD4): A Prospective Longitudinal Observational Study of Stargardt Disease Type 4, a PROM1- Related Macular Dystrophy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02410122
• Other study ID #: NA_00092688
• Status: Completed
• Start date: December 2014
• Est. completion date: March 2018

Study information

• Verified date: August 2018
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

While a fair amount of clinical data on Stargardt disease type 1 (STGD1) have been published, very little is known about Stargardt disease type 4 (STGD4). The ProgStar 04 study is an important opportunity to leverage the infrastructure, clinical trials sites, methods, and central reading center of the ProgStar program to investigate the progression of STGD4 and will help to establish patient cohorts worldwide for future clinical trials.

Description:

The PROM1 gene codes a protein called Prominin 1 (PROM1; also known as CD133 and AC133), most known for its original use as a human stem cell-specific marker. In the retina, PROM1 is involved in the formation and organization of disks within the outer segment (OS) of the photoreceptors. It is within this particular region that most of the electrochemical signals in response to light are generated (visual cycle-phototransduction). In STGD4, mutations in the PROM1 gene result in a defective isoform of the PROM1 protein that becomes trapped in the myoid region of the photoreceptors and cannot migrate to the OS site where disks are formed. Ultimately, the absence of PROM1 in the OS affects the growth and organization of the disks, which leads to disk malfunction and to vision problems.

Although many advances in genetic science have helped to recognize this variant of STGD, a comprehensive description of the natural history, including the variability in cone and rod dysfunction, of this STGD variant is not available. While there is no known treatment for STGD at this time, the preparation for future therapeutic approaches and for planning clinical trials must include an understanding of the disease itself, its variability, its progression and its correlation with visual loss. Moreover, clinical trials that aim to slow down the progression and/or to restore vision require validated outcome measures to prove treatment efficacy. However, such outcomes have not been established for STGD overall.

In summary, the characterization of STGD4-specific clinical manifestations, progression and prognosis as well as identification of outcome measures for clinical trials are critical to develop new clinical trials for STGD4. Hence, ProgStar 4 is developed as a prospective longitudinal observational study of patients with mutations in the PROM1 gene and a phenotype consistent with STGD.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: March 2018
• Est. primary completion date: March 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Years and older

Eligibility

Inclusion Criteria:

1. Provide a signed informed consent form and authorization allowing the disclosure and use of protected health information.

2. The designated primary study eye must have at least one well-demarcated area of atrophy. The lesion size should not exceed the area to be tracked in the OCT mode (20x20 degrees).

3. Have at least one pathogenic mutation confirmed in the PROM1 gene and a Stargardt phenotype.

4. The primary study eye must have clear ocular media and adequate pupillary dilation to permit good quality FAF and sd-OCT imaging in the opinion of the investigator.

5. Be able to cooperate in performing the examinations.

6. Be willing to undergo ocular examinations once every 6 months for up to 24 months.

7. Be at least six years old.

8. Both eyes can be included if inclusion criteria are fulfilled for both eyes.

Exclusion Criteria:

1. Ocular disease, such as choroidal neovascularization, glaucoma and diabetic retinopathy, in either eye that may confound assessment of the retina morphologically and functionally.

2. Intraocular surgery in the primary study eye within 90 days prior to baseline visit.

3. Current or previous participation in an interventional study to treat STGD such as gene therapy or stem cell therapy. Current participation in a drug trial or previous participation in a drug trial within six months before enrollment. The use of oral supplements of vitamins and minerals are permitted although the current use of Vitamin A supplementation shall be documented.

4. The site Principal Investigator may declare any patient at their site ineligible to participate in the study for a sound medical reason prior to the patient's enrollment into the study.

5. Any systemic disease with a limited survival prognosis (e.g. cancer, severe/unstable cardiovascular disease).

6. Any condition that would make adherence to the examination interfere with the patient attending their regular follow-up visits schedule of once every 6 months for up to 24 months difficult or unlikely, e.g. personality disorder, use of major tranquilizers such as Haldol or Phenothiazine, chronic alcoholism, Alzheimer's Disease or drug abuse.

7. Evidence of significant uncontrolled concomitant diseases such as cardiovascular, neurological, pulmonary, renal, hepatic, endocrine or gastro-intestinal disorders.

8. Patient is known to have one or more pathogenic mutation(s) in the ABCA4, RDS, or ELOVL4 genes.

Related Conditions & MeSH terms

• Atrophy
• Macular Degeneration
• Stargardt Disease

Locations

Country	Name	City	State
Germany	Universitäts-Augenklinik Bonn	Bonn
Germany	Center for Opthalmic Research, University of Tuebingen	Tuebingen
United Kingdom	Moorfields Eye Hospital	London
United States	Wilmer Eye Institute	Baltimore	Maryland
United States	Retina Foundation of the Southwest	Dallas	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Johns Hopkins University	The Shulsky Foundation

Countries where clinical trial is conducted

United States,  Germany,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Growth of atrophic lesions as measured by fundus autofluorescence (FAF) imaging		24 months
Secondary	Growth of atrophic lesions as measured by fundus autofluorescence (FAF) imaging		12 months
Secondary	Rate of retinal thinning and photoreceptor loss as measured by spectral domain optical coherence tomography (sd-OCT)		12 months
Secondary	Rate of retinal thinning and photoreceptor loss as measured by spectral domain optical coherence tomography (sd-OCT)		24 months
Secondary	Loss of retinal sensitivity as measured by microperimetry		12 months
Secondary	Loss of retinal sensitivity as measured by microperimetry		24 months
Secondary	Change in best-corrected visual acuity by using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol		12 months
Secondary	Change in best-corrected visual acuity by using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol		24 months
Secondary	Correlation of all outcome measures with genetic profile		12 months
Secondary	Correlation of all outcome measures with genetic profile		24 months

External Links

•   Click here for more information about this study: the Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar)