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	<title>Acquired C1 inhibitor deficiency &#8211; European Clinical Trials Information Network</title>
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	<title>Acquired C1 inhibitor deficiency &#8211; European Clinical Trials Information Network</title>
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		<title>Study to evaluate the efficacy and safety of deucrictibant for the prevention and treatment of angioedema attacks in adults with acquired angioedema</title>
		<link>https://clinicaltrials.eu/trial/study-to-evaluate-the-efficacy-and-safety-of-deucrictibant-for-the-prevention-and-treatment-of-angioedema-attacks-in-adults-with-acquired-angioedema/</link>
		
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		<pubDate>Wed, 29 Apr 2026 15:09:30 +0000</pubDate>
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					<description><![CDATA[This study is being conducted to evaluate the efficacy and safety of deucrictibant (PHA-022121) in adults with Acquired Angioedema due to C1 Inhibitor Deficiency. This condition is a rare disease that causes episodes of swelling, known as angioedema, which often occur in the face, hands, feet, or digestive tract. The research focuses on two different [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>This study is being conducted to evaluate the efficacy and safety of <b>deucrictibant</b> (<b>PHA-022121</b>) in adults with <b>Acquired Angioedema due to C1 Inhibitor Deficiency</b>. This condition is a rare disease that causes episodes of swelling, known as <b>angioedema</b>, which often occur in the face, hands, feet, or digestive tract. The research focuses on two different ways to use the medication: to prevent these swelling attacks from happening and to treat them as they occur.</p>
<p>The study is divided into three different parts. In the first part, participants take an extended-release tablet, which is a type of medication designed to release the drug slowly into the body over time, to see if it can prevent attacks. This part compares the drug to a <b>placebo</b>. The second part looks at using a soft capsule, which is a small, gel-like pill, to provide relief during an active attack. This part also compares the medication to a <b>placebo</b>. In the final part, participants receive the medication during an attack to monitor its safety and how well it is tolerated by the body.</p>
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