<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Zilucoplan</id>
	<title>Zilucoplan - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Zilucoplan"/>
	<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Zilucoplan&amp;action=history"/>
	<updated>2026-04-27T00:34:32Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
	<generator>MediaWiki 1.44.2</generator>
	<entry>
		<id>https://wikimd.org/index.php?title=Zilucoplan&amp;diff=5485597&amp;oldid=prev</id>
		<title>Prab at 20:51, 3 April 2024</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Zilucoplan&amp;diff=5485597&amp;oldid=prev"/>
		<updated>2024-04-03T20:51:03Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:Zilucoplan structure.svg|Zilucoplan structure|400px|right|thumb]]&lt;br /&gt;
{{svg-image}}&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Zilucoplan&amp;#039;&amp;#039;&amp;#039; is a [[Synthetic Peptides|synthetic macrocyclic peptide]] that functions as an inhibitor of the [[Complement System|terminal complement protein C5]], showcasing potential [[Anti-Inflammatory|anti-inflammatory]] and cell protective properties. Developed to address the unmet medical needs in conditions such as [[Paroxysmal Nocturnal Hemoglobinuria (PNH)]], [[Generalized Myasthenia Gravis (gMG)]], and [[Lupus Nephritis (LN)]], Zilucoplan offers a new approach to managing these complex diseases.&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Upon [[Subcutaneous Injection|subcutaneous administration]], Zilucoplan selectively binds to a distinct site on the terminal complement protein C5. This binding inhibits the cleavage of C5 into [[C5a]] and [[C5b]], pivotal steps in the activation of the complement system. By preventing this cleavage, Zilucoplan effectively halts the formation of the membrane-attack complex (MAC), a critical component in cell lysis and destruction observed in complement-mediated conditions.&lt;br /&gt;
&lt;br /&gt;
Furthermore, Zilucoplan blocks the interaction between C5b and [[C6]], further impeding the assembly of the MAC. This dual-action mechanism ensures a comprehensive inhibition of the terminal stages of the complement pathway, offering protection against MAC-mediated [[Red Blood Cells|red blood cells]] (RBCs) lysis and subsequent tissue damage.&lt;br /&gt;
&lt;br /&gt;
== Clinical Applications ==&lt;br /&gt;
Zilucoplan has been primarily investigated for its efficacy in treating diseases where complement-mediated damage plays a critical role:&lt;br /&gt;
&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Paroxysmal Nocturnal Hemoglobinuria (PNH):&amp;#039;&amp;#039;&amp;#039; A rare, life-threatening disease characterized by the destruction of red blood cells, leading to hemoglobinuria, anemia, and potential thrombosis.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Generalized Myasthenia Gravis (gMG):&amp;#039;&amp;#039;&amp;#039; A neuromuscular disorder resulting in muscle weakness and fatigue, where complement activation contributes to the damage of the neuromuscular junction.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Lupus Nephritis (LN):&amp;#039;&amp;#039;&amp;#039; A serious complication of systemic lupus erythematosus (SLE) that affects the kidneys, potentially leading to kidney failure.&lt;br /&gt;
&lt;br /&gt;
== Development and Approval ==&lt;br /&gt;
Zilucoplan&amp;#039;s development represents a collaborative effort between researchers and pharmaceutical companies to address the lack of targeted therapies for complement-mediated diseases. Its journey from discovery through to clinical trials highlights the potential for synthetic peptides in altering the treatment landscape for patients with PNH, gMG, and LN. Ongoing trials continue to evaluate the safety, efficacy, and optimal dosing of Zilucoplan, with the aim of achieving regulatory approval and broadening treatment options for patients suffering from these debilitating conditions.&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics and Administration ==&lt;br /&gt;
Administered through subcutaneous injection, Zilucoplan offers a patient-friendly alternative to intravenous treatments, potentially improving compliance and quality of life for individuals with chronic conditions requiring long-term management.&lt;br /&gt;
&lt;br /&gt;
== Future Directions ==&lt;br /&gt;
The exploration of Zilucoplan&amp;#039;s application beyond PNH, gMG, and LN to other complement-mediated diseases promises to expand its therapeutic reach, underscoring the versatility and potential of complement inhibitors in clinical practice.&lt;br /&gt;
{{stubd}}&lt;br /&gt;
{{Immunosuppressants}}&lt;br /&gt;
{{Complement system}}&lt;br /&gt;
{{Portal bar | Medicine}}&lt;br /&gt;
[[Category:Amino acid derivatives]]&lt;br /&gt;
[[Category:Complement system]]&lt;br /&gt;
[[Category:Cyclic peptides]]&lt;br /&gt;
[[Category:Immunosuppressants]]&lt;br /&gt;
[[Category:Orphan drugs]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
</feed>