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	<title>Progressive familial intrahepatic cholestasis &#8211; European Clinical Trials Information Network</title>
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	<title>Progressive familial intrahepatic cholestasis &#8211; European Clinical Trials Information Network</title>
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		<title>Study on Long-Term Safety and Effects of Maralixibat for Patients with Alagille Syndrome</title>
		<link>https://clinicaltrials.eu/trial/study-on-long-term-safety-and-effects-of-maralixibat-for-patients-with-alagille-syndrome/</link>
		
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		<pubDate>Wed, 29 Apr 2026 15:04:39 +0000</pubDate>
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					<description><![CDATA[This clinical trial is focused on studying Alagille syndrome, a rare genetic disorder that affects the liver and other parts of the body. The study will use a treatment called Livmarli, which is an oral solution containing the active substance maralixibat. The purpose of the study is to evaluate how well patients tolerate the treatment, [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>This clinical trial is focused on studying <i>Alagille syndrome</i>, a rare genetic disorder that affects the liver and other parts of the body. The study will use a treatment called <i>Livmarli</i>, which is an oral solution containing the active substance <i>maralixibat</i>. The purpose of the study is to evaluate how well patients tolerate the treatment, its long-term safety, and its effectiveness in managing symptoms of Alagille syndrome.</p>
<p>Participants in the study will take <i>Livmarli</i> as prescribed, and researchers will monitor them over an extended period. The study will look at various aspects, such as any side effects experienced, changes in liver function, and the severity of itching, which is a common symptom of the disease. The study will also observe how the treatment affects the levels of certain substances in the blood and the use of other medications for liver disease.</p>
<p>The trial aims to gather information on the safety of <i>Livmarli</i> over a long period, including any potential liver-related issues. It will also assess how well patients can tolerate the starting dose and any changes in dosage. The study will continue until 2035, providing valuable insights into the long-term management of <i>Alagille syndrome</i> with <i>Livmarli</i>.</p>
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