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● Active Not Recruiting
Study of Bitopertin in Participants With EPP or XLP (APOLLO)
Condition: Erythropoietic Protoporphyria (EPP) · X-Linked Protoporphyria (XLP) · Sponsor: Disc Medicine, Inc
About this study
The goal of this clinical trial is to learn if bitopertin works and is safe to treat EPP or XLP in participants 12 years or older. The main questions it aims to answer are: * Whether bitopertin increases pain-free sunlight exposure after 6 months of treatment in participants with EPP or XLP. * How PPIX concentration levels change from before bitopertin treatment to after 6 months of treatment. Researchers will compare bitopertin to a placebo look-alike substance that contains no drug. Participants will complete daily questionnaires and attend study visits for assessments.
This description comes directly from the study's public registry record.
Talk to the study team
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Locations (27)
| Marvel Clinical Research | Huntington Beach, California, United States | — |
| University of California San Francisco | San Francisco, California, United States | — |
| University of Miami Miller School of Medicine | Miami, Florida, United States | — |
| Massachusetts General Hospital | Boston, Massachusetts, United States | — |
| MetroBoston Clinical Partners | Boston, Massachusetts, United States | — |
| Henry Ford Health System | Detroit, Michigan, United States | — |
| Mount Sinai Hospital | New York, New York, United States | — |
| Wake Forest University | Winston-Salem, North Carolina, United States | — |
| Remington-Davis Clinical Research | Columbus, Ohio, United States | — |
| University of Texas Medical Branch | Galveston, Texas, United States | — |
| University of Washington | Seattle, Washington, United States | — |
| Royal Prince Alfred Hospital | Camperdown, New South Wales, Australia | — |
+ 15 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06910358