Narsoplimab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Human |
| Target | Mannan-binding lectin-associated serine protease-2 (MASP2) |
| Clinical data | |
| Trade names | Yartemlea |
| Other names | OMS-721, OMS620646, narsoplimab-wuug |
| License data |
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| Routes of administration | Intravenous |
| Drug class | Anti-inflammatory |
| ATC code |
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| Legal status | |
| Legal status | |
| Identifiers | |
| CAS Number | |
| DrugBank | |
| UNII | |
| KEGG | |
| Chemical and physical data | |
| Formula | C6340H9876N1680O1996S48 |
| Molar mass | 143109.39 g·mol−1 |
Narsoplimab, sold under the brand name Yartemlea, is a monoclonal antibody used for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy.[1][2] Narsoplimab is a mannan-binding lectin-associated serine protease-2 (MASP-2) inhibitor.[1] It is a recombinant human immunoglobulin G4 (IgG4) monoclonal antibody.[1]
Narsoplimab was approved for medical use in the United States in December 2025.[3]
Medical uses
Narsoplimab is indicated for the treatment of people with hematopoietic stem cell transplant-associated thrombotic microangiopathy.[1][2]
Hematopoietic stem cell transplant-associated thrombotic microangiopathy is a serious and life-threatening complication of hematopoietic stem cell transplant in which tiny blood clots form in the small blood vessels.[2] This can lead to organ damage, including damage to the kidneys, cardiovascular system, and gastrointestinal tract.[2]
Side effects
The most common side effects are viral infections, sepsis, hemorrhage, diarrhea, vomiting, nausea, neutropenia (low number of neutrophils, a type of white blood cell), fever, fatigue, and low potassium.[2]
Mechanism of action
Thrombotic microangiopathy is triggered by immunosuppressive treatment during stem cell transplant, especially when calcineurin and mTOR inhibitors are used.[4] It causes injury to endothelial cells, which is associated with an alteration of carbohydrate patterns on these cells, which is recognized by the complement system in the lectin pathway. Lectins are proteins that recognize specific glycoproteins, which is the main cause of microangiopathy during and after this procedure. Mannan-binding lectin-associated serine protease-2 (MASP-2) directly induces the coagulation cascade and the activation of C4 and C2 components. However, it can also bypass their activation by directly activating the C3 component, causing further activation of the terminal pathway and opsonization.[5]
Narsoplimab blocks the action of MASP-2.[1]
History
The efficacy of narsoplimab was assessed in a single-arm, open-label study (TA-TMA Study) of 28 participants, with additional data from 19 participants (6 pediatric participants and 13 adult participants) enrolled in an expanded access program.[2] In the TA-TMA Study, participants either received narsoplimab 4 mg/kg or 370 mg intravenously once weekly.[2]
Names
Narsoplimab is the international nonproprietary name.[6][7]
Narsoplimab is sold under the brand name Yartemlea.[1][2]
References
- ^ a b c d e f g "Archived copy" (PDF). Archived (PDF) from the original on 5 January 2026. Retrieved 6 January 2026.
{{cite web}}: CS1 maint: archived copy as title (link) - ^ a b c d e f g h "FDA approves first drug to treat serious complication of stem cell transplant". U.S. Food and Drug Administration (FDA). 5 January 2026. Retrieved 6 January 2026. This article incorporates text from this source, which is in the public domain.
- ^ "Novel Drug Approvals for 2025". U.S. Food and Drug Administration. 2 January 2026. Archived from the original on 3 March 2025. Retrieved 6 January 2026.
- ^ Khosla J, Yeh AC, Spitzer TR, Dey BR (February 2018). "Hematopoietic stem cell transplant-associated thrombotic microangiopathy: current paradigm and novel therapies". Bone Marrow Transplantation. 53 (2): 129–137. doi:10.1038/bmt.2017.207. PMID 28967899.
- ^ Merle NS, Church SE, Fremeaux-Bacchi V, Roumenina LT (2 June 2015). "Complement System Part I - Molecular Mechanisms of Activation and Regulation". Frontiers in Immunology. 6: 262. doi:10.3389/fimmu.2015.00262. ISSN 1664-3224. PMC 4451739. PMID 26082779.
- ^ World Health Organization (2020). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 83". WHO Drug Information. 34 (1). hdl:10665/339768.
- ^ World Health Organization (2021). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 85". WHO Drug Information. 35 (1). hdl:10665/340684.