Difference between revisions of "Romiplostim (Nplate)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
* 8/22/2008: Initial FDA approval
 
* 8/22/2008: Initial FDA approval
* 12/14/2018: Approved for pediatric patients 1 year of age and older with [[immune thrombocytopenia (ITP)]] for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy.
+
* 12/14/2018: Approved for pediatric patients 1 year of age and older with [[Immune thrombocytopenia|immune thrombocytopenia (ITP)]] for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy.
  
 
==Also known as==
 
==Also known as==

Revision as of 12:49, 8 May 2021

General information

Class/mechanism: Thrombopoietin (TPO/cMpl) receptor agonist. Romiplostim is an Fc-peptide fusion protein (peptibody) that interacts with the TPO receptor to trigger downstream signal cascades that ultimately stimulate platelet production by promoting proliferation and differentiation of megakaryocytes from bone marrow progenitor cells.[1][2][3]
Route: SC
Extravasation: n/a

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

  • 8/22/2008: Initial FDA approval
  • 12/14/2018: Approved for pediatric patients 1 year of age and older with immune thrombocytopenia (ITP) for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy.

Also known as

  • Brand name: Nplate

References