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Clinical Trials

September 20, 2021

Retina Foundation is Major Center for Next Phase of Gene Therapy for X-Linked Retinitis Pigmentosa: SKYLINE

X-linked retinitis pigmentosa (XLRP) is an inherited eye disease that causes gradual vision loss in boys and young men. The …

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Clinical Trials

August 26, 2021

Age-Related Macular Degeneration Happenings at the Foundation

At the Retina Foundation, our Laboratory Directors often partner with various pharmaceutical and biotechnology companies to conduct clinical trials and …

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Clinical Trials

June 29, 2021

Assessing Mobility Vision and Retinitis Pigmentosa

Scientists in the Rose-Silverthorne Retinal Degeneration Laboratory at the Retina Foundation recently began a new clinical trial utilizing a mobility …

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Clinical Trials

June 16, 2020

Choroideremia Research Is Necessary to Help Prevent Blindness at an Early Age

Choroideremia is an X-linked, recessive, inherited retinal disorder that affects 1 in 50,000 individuals. X-linked refers to the X chromosome, …

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Clinical Trials

October 1, 2019

Promising Results From Ongoing Phase 1/2 Clinical Trial for X-Linked Retinitis Pigmentosa (XLRP)

The Retina Foundation of the Southwest is one of four U.S. centers conducting a Phase 1/2 dose escalation, gene replacement …

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Clinical Trials

July 31, 2019

Retina Foundation Asks Kids to ‘Just Dance’ for Research Study

The Retina Foundation is an international leader in research on lazy eye, the most common cause of visual impairment in …

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Clinical Trials

July 23, 2019

Gene Therapy Trial for Choroideremia

In a clinical research study headed by Dr. David Birch, scientists in the Rose-Silverthorne Retinal Degenerations Lab are testing the …

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Clinical Trials

November 7, 2018

Phase III Treatment Trial for Stargardt Disease Enrolls First Patient

The Retina Foundation of the Southwest was the first site in the world to enroll patients in a new international …

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Clinical Trials

August 31, 2018

Retina Foundation Participates in International Effort to Treat Stargardt Disease

Stargardt disease is the most common form of inherited juvenile macular degeneration. Stargardt disease begins in late childhood and may …

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