VISTA Clinical Trial - AGTC HCP | Vista - AGTC HCP | Vista _Education & Science

XLRP Clinical TrialsGenetic TestingGene Therapy & IRDsResourcesRefer a PatientMale - 25XLRP DiagnosisExperiencing night blindness Male - 46RPGR MutationDiagnosis at age 10Legally blind by age 36 Male - 13XLRP DiagnosisFamily history of RPGR mutation The answer toGenetic Blindnessstarts with a clear visionThe focus is on investigational genetic therapies to restore visual function in patients with rare inherited retinal conditions.Learn more about our clinical trialsRefer a patientSee the possibilities for your patients.RPGR Mutation Male: 36 years oldVista clinical trial eligibilityYour patient may qualify to participate in the VISTA clinical trial, a phase 2/3 study evaluating an investigational gene therapy for the treatment of retinitis pigmentosa. Patients must meet the following criteria:Diagnosis of XLRP confirmed by a healthcare professionalHave a mutation in the RPGR gene confirmed by genetic testingMale ages 13-50 yearsPre-screening optionsRefer a patient for genetic testingHealthcare provider brochure See possibilities, not problems. Take the next step to find out more about resources available for you and your patients. Clinical Trial Opportunities The VISTA clinical trial is currently pre-screening male patients between the ages of 13-50 (inclusive) diagnosed with X-linked retinitis pigmentosa (XLRP). learn more Genetic TestingGenetic testing is critical to the diagnosis of patients with Inherited Retinal Disease. Learn more about the free genetic testing that may be available for your patients.learn more What is Gene Therapy?Gene therapy targets the exact cause of a disease and aims to treat the disease through a one-time administration.learn more Visionary science for life-changing curesAGTC is a biotechnology company seeking to transform the lives of patients with rare and debilitating eye diseases through its proprietary gene therapy platform.Our team includes industry-leading experts and innovative thinkers working together on discoveries that we hope will transform the lives of people with rare inherited eye disorders. In particular, we are studying how to use our gene therapy platform to develop investigational treatments for disorders that are caused by single-gene mutations and that also have a significant effect on a person’s sight.Learn more about AGTC and their groundbreaking investigational gene therapies for patients with rare diseases.Learn more at agtc.comThe answer to genetic Blindness starts with a CLEAR VISION.Refer a Patient for Pre-screeningRefer a Patient for Genetic TestingXLRP Clinical TrialsGenetic TestingGene Therapy & IRDsResourcesPrivacy Policy • Legal Notice • © 2022 AGTC • All rights reserved. | We respect confidentiality and privacy. Do not sell my dataWe use cookies to optimize site functionality and give you the best experience. Necessary cookies enable core functionality. The website cannot function properly without these cookies and can only be disabled by changing your browser preferences. 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