Peringatan Keamanan

In a single-dose toxicology study in rats, the no-observed adverse effect level (NOAEL) following IV administration was 40x106 MSC/kg and the maximum tolerated dose (MTD) was 65x106 MSCs/kg. The NOAEL was a cumulative dose of 80x106 MSC/kg when dosing twice per week in a repeat-dose study in rats, with no effects on host immune cell quantities or immune system functionality. There was no evidence of alloantibody formation.L11022

In a 6-week tumorigenicity study in mice, there was no evidence of tumor formation attributed to human mesenchymal stem cells. Standard genotoxicity and carcinogenicity studies, as well as animal reproduction and developmental toxicology studies were not conducted with remestmecel-L as they were not relevant for the aGvHD patient population.L11022

Remestemcel-L

DB13973

biotech approved investigational

Deskripsi

Remestemcel-L is a third-party, off-the-shelf suspension of ex-vivo cultured adult human mesenchymal stem cells intended for intravenous infusion. The mesenchymal stem cells are derived from the bone marrow of unrelated and human leukocyte antigen (HLA)–unmatched healthy adult donors and have the ability to differentiate into different tissue cells. It was approved for use in Canada in May 2012 as Prochymal for the management of refractory acute Graft versus Host Disease (aGvHD) in children who are unresponsive to systemic steroid therapies, with the approval conditional upon further trials being conducted.

aGvHD is a T-cell mediated disease that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues A31822 developed by 30-80% of the recipients A31818. aGvHD is often characterized by the presence of inflammatory cascades through signalling of activated T cells. While systemic corticosteroids and other immunosuppressive agents are commonly used as first-line treatments to manage aGvHD, about 30-50% of patients with aGvHD experience inadequately control of disease with first-line therapies, putting them in a risk for poor outcomes and creating a significant clinical challenge A31818. It is estimated that the patients with the most severe forms of refractory aGvHD that do not respond to steroid therapy have expected one-year survival rates of only 5% to 30% L11022. Human mesenchymal stem cells (hMSCs) serve to down-regulate inflammatory responses and produce anti-inflammatory cytokines and growth factors to promote tissue repair A31818. In clinical studies, patients treated with remestemcel-L demonstrated an improvement in their aGvHD and improved survival rates at subsequent days following intravenous infusion L11022. Based on its tolerability and safety profile, remestemcel-L is a promising alternative to second-line immunosuppressive agents A31818.

Struktur Molekul 2D

Struktur tidak tersedia

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) -
Volume Distribusi -
Klirens (Clearance) -

Absorpsi

Following intravenous infusion, distribution of remestemcel-L to the lungs within minutes of infusion was observed in several in vivo biodistribution studies of healthy animals. Based on findings of total body irradiation studies of animals, remestemcel-L will preferentially distribute to sites of inflammation and tissue damage such as the bone marrow, GI tract, and skin, the organs that have sustained the most tissue damage.L11022

Metabolisme

The metabolism of cellular components (nucleic acids, amino acids, lipids, etc) in the normal course of cell turnover in the body is well understood. It is expected that the infused cells will be metabolized the same way; therefore these studies were not conducted.L11022

Rute Eliminasi

The excretion of cellular components (nucleic acids, amino acids, lipids, etc) in the normal course of cell turnover in the body is well understood. It is expected that the infused cells will be metabolized the same way; therefore these studies were not conducted.L11022

Interaksi Obat

0 Data
Tidak ada data.

Referensi & Sumber

Artikel (PubMed)
  • PMID: 24216185
    Kurtzberg J, Prockop S, Teira P, Bittencourt H, Lewis V, Chan KW, Horn B, Yu L, Talano JA, Nemecek E, Mills CR, Chaudhury S: Allogeneic human mesenchymal stem cell therapy (remestemcel-L, Prochymal) as a rescue agent for severe refractory acute graft-versus-host disease in pediatric patients. Biol Blood Marrow Transplant. 2014 Feb;20(2):229-35. doi: 10.1016/j.bbmt.2013.11.001. Epub 2013 Nov 8.
  • PMID: 14735553
    Reddy P: Pathophysiology of acute graft-versus-host disease. Hematol Oncol. 2003 Dec;21(4):149-61. doi: 10.1002/hon.716.
  • PMID: 15882431
    Jaksch M, Mattsson J: The pathophysiology of acute graft-versus-host disease. Scand J Immunol. 2005 May;61(5):398-409. doi: 10.1111/j.1365-3083.2005.01595.x.
  • PMID: 23574329
    Tobin LM, Healy ME, English K, Mahon BP: Human mesenchymal stem cells suppress donor CD4(+) T cell proliferation and reduce pathology in a humanized mouse model of acute graft-versus-host disease. Clin Exp Immunol. 2013 May;172(2):333-48. doi: 10.1111/cei.12056.
  • PMID: 24903975
    Amorin B, Alegretti AP, Valim V, Pezzi A, Laureano AM, da Silva MA, Wieck A, Silla L: Mesenchymal stem cell therapy and acute graft-versus-host disease: a review. Hum Cell. 2014 Oct;27(4):137-50. doi: 10.1007/s13577-014-0095-x. Epub 2014 Jun 6.
  • PMID: 17784964
    Jacobsohn DA, Vogelsang GB: Acute graft versus host disease. Orphanet J Rare Dis. 2007 Sep 4;2:35. doi: 10.1186/1750-1172-2-35.

Contoh Produk & Brand

Produk: 1 • International brands: 2
Produk
  • Prochymal
    Solution • 100000000 unit / 15 mL • Intravenous • Canada • Approved
International Brands
  • NestaCell
  • Prochymal

Sekuens Gen/Protein (FASTA)

Sekuens dimuat saat dibutuhkan agar halaman tetap ringan.
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