CR002

DB05139

biotech investigational

Deskripsi

CR002 is a novel investigational fully human monoclonal antibody that blocks the activity of excess platelet-derived growth factor-D (PDGF-D), a target shown to play a role in kidney inflammation. This is a novel therapeutic approach to treat kidney inflammation.

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

Data absorpsi tidak tersedia.

Metabolisme

Data metabolisme tidak tersedia.

Rute Eliminasi

Data eliminasi belum tersedia.

Interaksi Obat

372 Data
Diethylstilbestrol Diethylstilbestrol may increase the thrombogenic activities of CR002.
Chlorotrianisene Chlorotrianisene may increase the thrombogenic activities of CR002.
Conjugated estrogens Conjugated estrogens may increase the thrombogenic activities of CR002.
Estrone Estrone may increase the thrombogenic activities of CR002.
Estradiol Estradiol may increase the thrombogenic activities of CR002.
Dienestrol Dienestrol may increase the thrombogenic activities of CR002.
Ethinylestradiol Ethinylestradiol may increase the thrombogenic activities of CR002.
Mestranol Mestranol may increase the thrombogenic activities of CR002.
Estriol Estriol may increase the thrombogenic activities of CR002.
Estrone sulfate Estrone sulfate may increase the thrombogenic activities of CR002.
Quinestrol Quinestrol may increase the thrombogenic activities of CR002.
Hexestrol Hexestrol may increase the thrombogenic activities of CR002.
Tibolone Tibolone may increase the thrombogenic activities of CR002.
Synthetic Conjugated Estrogens, A Synthetic Conjugated Estrogens, A may increase the thrombogenic activities of CR002.
Synthetic Conjugated Estrogens, B Synthetic Conjugated Estrogens, B may increase the thrombogenic activities of CR002.
Polyestradiol phosphate Polyestradiol phosphate may increase the thrombogenic activities of CR002.
Esterified estrogens Esterified estrogens may increase the thrombogenic activities of CR002.
Zeranol Zeranol may increase the thrombogenic activities of CR002.
Equol Equol may increase the thrombogenic activities of CR002.
Promestriene Promestriene may increase the thrombogenic activities of CR002.
Methallenestril Methallenestril may increase the thrombogenic activities of CR002.
Epimestrol Epimestrol may increase the thrombogenic activities of CR002.
Moxestrol Moxestrol may increase the thrombogenic activities of CR002.
Estradiol acetate Estradiol acetate may increase the thrombogenic activities of CR002.
Estradiol benzoate Estradiol benzoate may increase the thrombogenic activities of CR002.
Estradiol cypionate Estradiol cypionate may increase the thrombogenic activities of CR002.
Estradiol valerate Estradiol valerate may increase the thrombogenic activities of CR002.
Biochanin A Biochanin A may increase the thrombogenic activities of CR002.
Formononetin Formononetin may increase the thrombogenic activities of CR002.
Estetrol Estetrol may increase the thrombogenic activities of CR002.
Cetuximab The risk or severity of adverse effects can be increased when Cetuximab is combined with CR002.
Human immunoglobulin G The risk or severity of adverse effects can be increased when Human immunoglobulin G is combined with CR002.
Omalizumab The risk or severity of adverse effects can be increased when Omalizumab is combined with CR002.
Adalimumab The risk or severity of adverse effects can be increased when Adalimumab is combined with CR002.
Abciximab The risk or severity of adverse effects can be increased when Abciximab is combined with CR002.
Gemtuzumab ozogamicin The risk or severity of adverse effects can be increased when Gemtuzumab ozogamicin is combined with CR002.
Indium In-111 satumomab pendetide The risk or severity of adverse effects can be increased when Indium In-111 satumomab pendetide is combined with CR002.
Infliximab The risk or severity of adverse effects can be increased when Infliximab is combined with CR002.
Trastuzumab The risk or severity of adverse effects can be increased when Trastuzumab is combined with CR002.
Rituximab The risk or severity of adverse effects can be increased when Rituximab is combined with CR002.
Basiliximab The risk or severity of adverse effects can be increased when Basiliximab is combined with CR002.
Muromonab The risk or severity of adverse effects can be increased when Muromonab is combined with CR002.
Digoxin Immune Fab (Ovine) The risk or severity of adverse effects can be increased when Digoxin Immune Fab (Ovine) is combined with CR002.
Ibritumomab tiuxetan The risk or severity of adverse effects can be increased when Ibritumomab tiuxetan is combined with CR002.
Tositumomab The risk or severity of adverse effects can be increased when Tositumomab is combined with CR002.
Alemtuzumab The risk or severity of adverse effects can be increased when Alemtuzumab is combined with CR002.
Capromab pendetide The risk or severity of adverse effects can be increased when Capromab pendetide is combined with CR002.
Efalizumab The risk or severity of adverse effects can be increased when Efalizumab is combined with CR002.
Antithymocyte immunoglobulin (rabbit) The risk or severity of adverse effects can be increased when Antithymocyte immunoglobulin (rabbit) is combined with CR002.
Natalizumab The risk or severity of adverse effects can be increased when Natalizumab is combined with CR002.
Palivizumab The risk or severity of adverse effects can be increased when Palivizumab is combined with CR002.
Daclizumab The risk or severity of adverse effects can be increased when Daclizumab is combined with CR002.
Bevacizumab The risk or severity of adverse effects can be increased when Bevacizumab is combined with CR002.
Technetium Tc-99m arcitumomab The risk or severity of adverse effects can be increased when Technetium Tc-99m arcitumomab is combined with CR002.
Eculizumab The risk or severity of adverse effects can be increased when Eculizumab is combined with CR002.
Panitumumab The risk or severity of adverse effects can be increased when Panitumumab is combined with CR002.
Ranibizumab The risk or severity of adverse effects can be increased when Ranibizumab is combined with CR002.
Galiximab The risk or severity of adverse effects can be increased when Galiximab is combined with CR002.
Pexelizumab The risk or severity of adverse effects can be increased when Pexelizumab is combined with CR002.
Afelimomab The risk or severity of adverse effects can be increased when Afelimomab is combined with CR002.
Epratuzumab The risk or severity of adverse effects can be increased when Epratuzumab is combined with CR002.
Bectumomab The risk or severity of adverse effects can be increased when Bectumomab is combined with CR002.
Oregovomab The risk or severity of adverse effects can be increased when Oregovomab is combined with CR002.
IGN311 The risk or severity of adverse effects can be increased when IGN311 is combined with CR002.
Adecatumumab The risk or severity of adverse effects can be increased when Adecatumumab is combined with CR002.
Labetuzumab The risk or severity of adverse effects can be increased when Labetuzumab is combined with CR002.
Matuzumab The risk or severity of adverse effects can be increased when Matuzumab is combined with CR002.
Fontolizumab The risk or severity of adverse effects can be increased when Fontolizumab is combined with CR002.
Bavituximab The risk or severity of adverse effects can be increased when Bavituximab is combined with CR002.
Rozrolimupab The risk or severity of adverse effects can be increased when CR002 is combined with Rozrolimupab.
Girentuximab The risk or severity of adverse effects can be increased when CR002 is combined with Girentuximab.
Obiltoxaximab The risk or severity of adverse effects can be increased when CR002 is combined with Obiltoxaximab.
XTL-001 The risk or severity of adverse effects can be increased when CR002 is combined with XTL-001.
NAV 1800 The risk or severity of adverse effects can be increased when CR002 is combined with NAV 1800.
Briakinumab The risk or severity of adverse effects can be increased when CR002 is combined with Briakinumab.
Otelixizumab The risk or severity of adverse effects can be increased when CR002 is combined with Otelixizumab.
AMG 108 The risk or severity of adverse effects can be increased when CR002 is combined with AMG 108.
Iratumumab The risk or severity of adverse effects can be increased when CR002 is combined with Iratumumab.
Enokizumab The risk or severity of adverse effects can be increased when CR002 is combined with Enokizumab.
Ramucirumab The risk or severity of adverse effects can be increased when CR002 is combined with Ramucirumab.
Farletuzumab The risk or severity of adverse effects can be increased when CR002 is combined with Farletuzumab.
Veltuzumab The risk or severity of adverse effects can be increased when CR002 is combined with Veltuzumab.
Ustekinumab The risk or severity of adverse effects can be increased when CR002 is combined with Ustekinumab.
Trastuzumab emtansine The risk or severity of adverse effects can be increased when CR002 is combined with Trastuzumab emtansine.
PRO-542 The risk or severity of adverse effects can be increased when CR002 is combined with PRO-542.
TNX-901 The risk or severity of adverse effects can be increased when CR002 is combined with TNX-901.
Inotuzumab ozogamicin The risk or severity of adverse effects can be increased when CR002 is combined with Inotuzumab ozogamicin.
RI 624 The risk or severity of adverse effects can be increased when CR002 is combined with RI 624.
Stamulumab The risk or severity of adverse effects can be increased when CR002 is combined with MYO-029.
CT-011 The risk or severity of adverse effects can be increased when CR002 is combined with CT-011.
Leronlimab The risk or severity of adverse effects can be increased when CR002 is combined with Leronlimab.
Glembatumumab vedotin The risk or severity of adverse effects can be increased when CR002 is combined with Glembatumumab vedotin.
Olaratumab The risk or severity of adverse effects can be increased when CR002 is combined with Olaratumab.
IPH 2101 The risk or severity of adverse effects can be increased when CR002 is combined with IPH 2101.
TB-402 The risk or severity of adverse effects can be increased when CR002 is combined with TB-402.
Caplacizumab The risk or severity of adverse effects can be increased when CR002 is combined with Caplacizumab.
IMC-1C11 The risk or severity of adverse effects can be increased when CR002 is combined with IMC-1C11.
Eldelumab The risk or severity of adverse effects can be increased when CR002 is combined with Eldelumab.
Lumiliximab The risk or severity of adverse effects can be increased when CR002 is combined with Lumiliximab.
Canakinumab The risk or severity of adverse effects can be increased when CR002 is combined with Canakinumab.

Target Protein

Platelet-derived growth factor D PDGFD

Referensi & Sumber

Artikel (PubMed)
  • PMID: 17308324
    Boor P, Konieczny A, Villa L, Kunter U, van Roeyen CR, LaRochelle WJ, Smithson G, Arrol S, Ostendorf T, Floege J: PDGF-D inhibition by CR002 ameliorates tubulointerstitial fibrosis following experimental glomerulonephritis. Nephrol Dial Transplant. 2007 May;22(5):1323-31. Epub 2007 Feb 17.
  • PMID: 16510766
    Ostendorf T, Rong S, Boor P, Wiedemann S, Kunter U, Haubold U, van Roeyen CR, Eitner F, Kawachi H, Starling G, Alvarez E, Smithson G, Floege J: Antagonism of PDGF-D by human antibody CR002 prevents renal scarring in experimental glomerulonephritis. J Am Soc Nephrol. 2006 Apr;17(4):1054-62. Epub 2006 Mar 1.
  • PMID: 12937299
    Ostendorf T, van Roeyen CR, Peterson JD, Kunter U, Eitner F, Hamad AJ, Chan G, Jia XC, Macaluso J, Gazit-Bornstein G, Keyt BA, Lichenstein HS, LaRochelle WJ, Floege J: A fully human monoclonal antibody (CR002) identifies PDGF-D as a novel mediator of mesangioproliferative glomerulonephritis. J Am Soc Nephrol. 2003 Sep;14(9):2237-47.

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