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Amy Pikalek

BIM2

Posted on December 1, 2020

To identify whether genetic variation or polymorphism in genes that impact angiogenesis can be identified as biomarkers for responsiveness to anti-VEGF therapy in patients with neovascular age-related macular degeneration.

Posted in Age-related Macular Degeneration, Barbara Blodi, Clinical Trials, Genetics

GENETIC EYE DISORDERS

Posted on December 1, 2020

To identify the gene or genes responsible for developmental causes of blindness in the world, and to establish a Pediatric Ophthalmic Genetics and Research Program at the University of Wisconsin–Madison.

Posted in Actively Recruiting, Clinical Trials, Genetics, Terri Young, Young Lab

XOLARIS

Posted on December 1, 2020

To gain a better understanding of disease progression over time in male subjects with X-linked retinitis pigmentosa (XLRP).

Posted in Clinical Trials, Inherited Retinal Degeneration, Kimberly Stepien, Past

CHM SURVEY TRIAL

Posted on December 1, 2020

Choroideremia (CHM) Health Outcomes

Posted in Choroideremia, Clinical Trials, Inherited Retinal Degeneration, Kimberly Stepien, Past

CATALINA

Posted on December 1, 2020

A Phase II Multicenter, Randomized, Double-Masked, Sham-Controlled Study of the Safety and Efficacy of Intravitreal Injections of NGM621 in Subjects with Geographic Atrophy (GA) Secondary to Age-Related Macular Degeneration (AMD) (CATALINA)

Posted in Age-related Macular Degeneration, Clinical Trials, Geographic Atrophy, Kathleen Schildroth, Past

Meet Alicia Wolf, Social Worker with UW Health Patient Resources

Posted on November 3, 2020

Patient Services in Action: Alicia Wolf       As the social worker for ophthalmology services, Alicia Wolf has been assisting our providers in connecting their patients to resources to cope with low vision, as …

Posted in Age-related Macular Degeneration, News, Vision Rehab

Pro-EYS

Posted on September 30, 2020

Rate of Progression in EYS Related Retinal Degeneration (Pro-EYS).

Posted in Clinical Trials, Genetic mutation, Inherited Retinal Degeneration, Kimberly Stepien, Ongoing

AGTC A3

Posted on September 30, 2020

A Multiple-Site, Phase 1/2, Safety and Efficacy Trial of AGTC 402, a Recombinant Adeno-associated Virus Vector Expressing CNGA3, in Patients with Congenital Achromatopsia Caused by Mutations in the CNGA3 Gene

Posted in Clinical Trials, Congenital Achromatopsia, Genetic mutation, Inherited Retinal Degeneration, Kimberly Stepien, Past

AGTC B3

Posted on September 30, 2020

A Multiple-Site, Phase 1/2, Safety and Efficacy Trial of a Recombinant Adeno-associated Virus Vector Expressing CNGB3 (rAAV2tYF-PR1.7-hCNGB3) in Patients with Congenital Achromatopsia Caused by Mutations in the CNGB3 Gene

Posted in Clinical Trials, Congenital Achromatopsia, Genetic mutation, Inherited Retinal Degeneration, Kimberly Stepien, Past
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