Condition: Retinitis Pigmentosa · Sponsor: Sumitomo Pharma America, Inc.
The Goal of this study is to evaluate the safety, tolerability, and clinical responses following single dose of DSP-3077. Study enrolls both male and female patients in 3 cohorts with each cohort defined by visual acuity (VA) criteria and dose level of DSP-3077. Each cohort will include 4 participants.
This description comes directly from the study's public registry record.
Contact details are listed per location below or on the registry record.
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| Massachusetts Eye and Ear | Boston, Massachusetts, United States | Recruiting |
| University of Minnesota | Minneapolis, Minnesota, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06891885