Condition: Erythropoietic Protoporphyria (EPP) · X-Linked Porphyria (XLP) · Sponsor: Portal Therapeutics, Inc.
The purpose of this study is to collect information about the effects of EPP/XLP in adults and adolescents. This is an observational study in which participants will not receive any treatment. Study details include: * The study duration will be up to 6 months for each participant. * After Screening, participants will have a Baseline (Day 1) visit and return for visits every 4 weeks through 24 weeks. * Assessments to evaluate EPP/XLP will include clinical laboratory tests, physical exams, vital signs measurement, blood draws for PPIX concentration, reporting of EPP/XLP-related symptoms (including completion of a daily diary), light dosimetry.
This description comes directly from the study's public registry record.
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| Massachusetts General Hospital | Boston, Massachusetts, United States | Recruiting |
| Mount Sinai School of Medicine | New York, New York, United States | Recruiting |
| Wake Forest University Baptist Health - Dept of Gastroenterology | Wake Forest, North Carolina, United States | Recruiting |
| Temple University | Philadelphia, Pennsylvania, United States | Not Yet Recruiting |
| University of Texas Health - Ertan Digestive Disease Center | Houston, Texas, United States | Recruiting |
| UZ Leuven | Leuven, Belgium | Not Yet Recruiting |
| University of Alberta Hospital | Edmonton, Canada | Not Yet Recruiting |
| Centre Hospitalier Universitaire de Bordeaux - Hopital Saint - Andre | Bordeaux, France | Not Yet Recruiting |
| AP-HP Hopital Bichat - Claude Bernard | Paris, France | Not Yet Recruiting |
| Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano | Milan, Italy | Not Yet Recruiting |
| Azienda Ospedaliero-Universitaria di Modena | Modena, Italy | Not Yet Recruiting |
| Haukeland University Hospital | Bergen, Norway | Not Yet Recruiting |
+ 7 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07567131