Azienda Ospedaliero Universitaria Di Modena
Verified
Modena, Italy
Rare diseases
Investigational molecules
Locations
A plain-language summary of the goals, design and what participants do
This clinical trial is focused on studying two rare conditions: Erythropoietic Protoporphyria (EPP) and X-Linked Protoporphyria (XLP). These are genetic disorders that cause sensitivity to sunlight, leading to painful skin reactions. The study is testing a medication called Dersimelagon, also known by its code name MT-7117. This medication is taken orally in the form of a tablet.
The purpose of the study is to evaluate the long-term safety and tolerability of Dersimelagon in individuals with EPP or XLP. Participants in the study will take the medication over an extended period, and their health will be monitored to ensure the treatment is safe and well-tolerated. The study will involve regular check-ups, including physical exams and laboratory tests, to track any changes in health and to identify any potential side effects.
Throughout the study, participants will be closely observed for any treatment-emergent adverse events, which are any new or worsening health issues that occur during the study. This includes serious adverse events and any other health concerns that may arise. The study aims to provide valuable information on the long-term use of Dersimelagon for managing EPP and XLP, contributing to better understanding and treatment of these conditions.
The trial runs in 4 steps – from screening to follow-up. Each step says what happens and what the team monitors.
7 criteria
5 criteria
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Modena, Italy
Sassari, Italy
Rotterdam, The Netherlands
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This is a rare genetic disorder that affects the production of heme, a component of hemoglobin. It leads to a buildup of protoporphyrin in the blood, which can cause sensitivity to sunlight. Individuals with this condition often experience painful skin reactions after exposure to sunlight, including burning, itching, and swelling. Over time, repeated sun exposure can lead to changes in skin texture and appearance. The condition is usually diagnosed in childhood and can significantly impact daily activities due to the need to avoid sunlight.
This is a genetic disorder similar to erythropoietic protoporphyria, but it is linked to the X chromosome. It also results in the accumulation of protoporphyrin in the blood, causing sensitivity to sunlight. Affected individuals may experience severe pain, redness, and swelling of the skin after sun exposure. The condition can lead to chronic skin changes and scarring over time. It is typically identified in early childhood and requires careful management to avoid sun exposure. The disorder is more common in males due to its X-linked inheritance pattern.
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