Journal of Bone and Mineral Research, ISSN 0884-0431, 10/2006, Volume 21, Issue 10, pp. 1571 - 1580
Lung cancer metastases to bone produce a primarily mixed osteolytic/osteoblastic lesion. The purpose of this study was to determine if blockade of both...
RANK:Fc protein | RANK ligand | RANK | bone metastasis | osteoclastogenesis | noggin | Noggin | Osteoclastogenesis | Bone metastasis | Bone Morphogenetic Proteins - antagonists & inhibitors | Neoplasm Transplantation | Bone Neoplasms - therapy | Humans | Lung Neoplasms - metabolism | Recombinant Fusion Proteins - therapeutic use | Bone Neoplasms - secondary | Lung Neoplasms - pathology | Male | Bone Neoplasms - pathology | Tibia - pathology | Carcinoma, Non-Small-Cell Lung - pathology | Cytokines - metabolism | Carcinoma, Non-Small-Cell Lung - metabolism | Tibia - diagnostic imaging | Mice, SCID | Osteoclasts - metabolism | Osteolysis - metabolism | Radiography | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Cell Line, Tumor | Mice | Osteoclasts - drug effects
RANK:Fc protein | RANK ligand | RANK | bone metastasis | osteoclastogenesis | noggin | Noggin | Osteoclastogenesis | Bone metastasis | Bone Morphogenetic Proteins - antagonists & inhibitors | Neoplasm Transplantation | Bone Neoplasms - therapy | Humans | Lung Neoplasms - metabolism | Recombinant Fusion Proteins - therapeutic use | Bone Neoplasms - secondary | Lung Neoplasms - pathology | Male | Bone Neoplasms - pathology | Tibia - pathology | Carcinoma, Non-Small-Cell Lung - pathology | Cytokines - metabolism | Carcinoma, Non-Small-Cell Lung - metabolism | Tibia - diagnostic imaging | Mice, SCID | Osteoclasts - metabolism | Osteolysis - metabolism | Radiography | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Cell Line, Tumor | Mice | Osteoclasts - drug effects
Journal Article
JOURNAL OF BONE AND MINERAL RESEARCH, ISSN 0884-0431, 10/2006, Volume 21, Issue 10, pp. 1571 - 1580
Lung cancer metastases to bone produce a primarily mixed osteolytic/osteoblastic lesion. The purpose of this study was to determine if blockade of both...
RANK ligand | bone metastasis | OSTEOLYTIC LESIONS | noggin | BMP SIGNALING INHIBITION | RANK | BREAST-CANCER | OSTEOCLAST DEPLETION | PROSTATE-CANCER | IN-VIVO | ENDOCRINOLOGY & METABOLISM | RECEPTOR ACTIVATOR | RANK : Fc protein | CYSTINE KNOT PROTEIN | osteoclastogenesis | KAPPA-B LIGAND | MORPHOGENETIC PROTEIN-2
RANK ligand | bone metastasis | OSTEOLYTIC LESIONS | noggin | BMP SIGNALING INHIBITION | RANK | BREAST-CANCER | OSTEOCLAST DEPLETION | PROSTATE-CANCER | IN-VIVO | ENDOCRINOLOGY & METABOLISM | RECEPTOR ACTIVATOR | RANK : Fc protein | CYSTINE KNOT PROTEIN | osteoclastogenesis | KAPPA-B LIGAND | MORPHOGENETIC PROTEIN-2
Journal Article
Blood, ISSN 0006-4971, 03/2012, Volume 119, Issue 13, pp. 3031 - 3037
Current factor VIII (FVIII) products display a half-life (t(1/2)) of similar to 8-12 hours, requiring frequent intravenous injections for prophylaxis and...
PROPHYLACTIC TREATMENT | IMPACT | THERAPY | ORTHOPEDIC STATUS | PROGRESS | TAILORED PROPHYLAXIS | OUTCOMES | HEMATOLOGY | VON-WILLEBRAND-FACTOR | CHILDREN | Recombinant Fusion Proteins - adverse effects | Factor VIII - pharmacokinetics | Humans | Middle Aged | Receptors, Fc - metabolism | Recombinant Fusion Proteins - therapeutic use | Half-Life | Male | Metabolic Clearance Rate | Immunoglobulin Fc Fragments - administration & dosage | Receptors, Fc - therapeutic use | Dose-Response Relationship, Drug | Young Adult | Time Factors | Adult | Factor VIII - adverse effects | Immunoglobulin Fc Fragments - therapeutic use | Immunoglobulin Fc Fragments - adverse effects | Recombinant Fusion Proteins - administration & dosage | Factor VIII - therapeutic use | von Willebrand Factor - analysis | Infusion Pumps | Hemophilia A - blood | Hemophilia A - metabolism | Receptors, Fc - administration & dosage | Recombinant Fusion Proteins - pharmacokinetics | Factor VIII - administration & dosage | Hemophilia A - drug therapy | Clinical Trials and Observations
PROPHYLACTIC TREATMENT | IMPACT | THERAPY | ORTHOPEDIC STATUS | PROGRESS | TAILORED PROPHYLAXIS | OUTCOMES | HEMATOLOGY | VON-WILLEBRAND-FACTOR | CHILDREN | Recombinant Fusion Proteins - adverse effects | Factor VIII - pharmacokinetics | Humans | Middle Aged | Receptors, Fc - metabolism | Recombinant Fusion Proteins - therapeutic use | Half-Life | Male | Metabolic Clearance Rate | Immunoglobulin Fc Fragments - administration & dosage | Receptors, Fc - therapeutic use | Dose-Response Relationship, Drug | Young Adult | Time Factors | Adult | Factor VIII - adverse effects | Immunoglobulin Fc Fragments - therapeutic use | Immunoglobulin Fc Fragments - adverse effects | Recombinant Fusion Proteins - administration & dosage | Factor VIII - therapeutic use | von Willebrand Factor - analysis | Infusion Pumps | Hemophilia A - blood | Hemophilia A - metabolism | Receptors, Fc - administration & dosage | Recombinant Fusion Proteins - pharmacokinetics | Factor VIII - administration & dosage | Hemophilia A - drug therapy | Clinical Trials and Observations
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 12/2016, Volume 22, Issue 23, pp. 5898 - 5908
Purpose: The induction of tissue-localized virus-specific CD8 T-cell response is essential for the development of an effective therapeutic vaccine against...
GAMMA | RESPONSES | CLINICAL-TRIAL | ONCOLOGY | FEMALE GENITAL-TRACT | HELPER-CELLS | RECEPTOR | HUMAN-PAPILLOMAVIRUS | INTRAEPITHELIAL NEOPLASIA | LESIONS | IL-7 | Dendritic Cells - immunology | Mice, Inbred C57BL | Vaccines, DNA - immunology | Uterine Cervical Neoplasms - immunology | Administration, Intravaginal | Alphapapillomavirus - immunology | Interleukin-7 - administration & dosage | Cancer Vaccines - immunology | Immunity, Cellular - immunology | Animals | Interleukin-7 - immunology | Vaccination - methods | Papillomavirus Infections - immunology | Uterine Cervical Neoplasms - virology | Female | Papillomavirus Vaccines - immunology | Mice | CD8-Positive T-Lymphocytes - immunology | Cytokines - immunology
GAMMA | RESPONSES | CLINICAL-TRIAL | ONCOLOGY | FEMALE GENITAL-TRACT | HELPER-CELLS | RECEPTOR | HUMAN-PAPILLOMAVIRUS | INTRAEPITHELIAL NEOPLASIA | LESIONS | IL-7 | Dendritic Cells - immunology | Mice, Inbred C57BL | Vaccines, DNA - immunology | Uterine Cervical Neoplasms - immunology | Administration, Intravaginal | Alphapapillomavirus - immunology | Interleukin-7 - administration & dosage | Cancer Vaccines - immunology | Immunity, Cellular - immunology | Animals | Interleukin-7 - immunology | Vaccination - methods | Papillomavirus Infections - immunology | Uterine Cervical Neoplasms - virology | Female | Papillomavirus Vaccines - immunology | Mice | CD8-Positive T-Lymphocytes - immunology | Cytokines - immunology
Journal Article
Expert Opinion on Biological Therapy, ISSN 1471-2598, 07/2016, Volume 16, Issue 7, pp. 903 - 915
Introduction: Many of the biotherapeutics approved or under development suffer from a short half-life necessitating frequent applications in order to maintain...
polymer | half-life extension | fusion protein | PEGylation | Albumin | FcRn | glycosylation | Fc region | MEDICINE, RESEARCH & EXPERIMENTAL | SINGLE-CHAIN DIABODY | LONG-ACTING ERYTHROPOIETIN | FACTOR VIIA | GONADOTROPIN-BETA-SUBUNIT | ALBUMIN-BINDING DOMAIN | PH-DEPENDENT BINDING | NEONATAL FC-RECEPTOR | GLUCAGON-LIKE PEPTIDE-1 | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CARBOXYL-TERMINAL PEPTIDE | Biological Therapy - methods | Biological Therapy - trends | Albumins - metabolism | Immunoglobulin Fc Fragments - metabolism | Humans | Receptors, Fc - metabolism | Half-Life | Albumins - administration & dosage | Glycosylation - drug effects | Immunoglobulin Fc Fragments - administration & dosage | Histocompatibility Antigens Class I - metabolism | Animals | Receptors, Fc - administration & dosage | Histocompatibility Antigens Class I - administration & dosage
polymer | half-life extension | fusion protein | PEGylation | Albumin | FcRn | glycosylation | Fc region | MEDICINE, RESEARCH & EXPERIMENTAL | SINGLE-CHAIN DIABODY | LONG-ACTING ERYTHROPOIETIN | FACTOR VIIA | GONADOTROPIN-BETA-SUBUNIT | ALBUMIN-BINDING DOMAIN | PH-DEPENDENT BINDING | NEONATAL FC-RECEPTOR | GLUCAGON-LIKE PEPTIDE-1 | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CARBOXYL-TERMINAL PEPTIDE | Biological Therapy - methods | Biological Therapy - trends | Albumins - metabolism | Immunoglobulin Fc Fragments - metabolism | Humans | Receptors, Fc - metabolism | Half-Life | Albumins - administration & dosage | Glycosylation - drug effects | Immunoglobulin Fc Fragments - administration & dosage | Histocompatibility Antigens Class I - metabolism | Animals | Receptors, Fc - administration & dosage | Histocompatibility Antigens Class I - administration & dosage
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 05/2016, Volume 63, Issue 5, pp. 922 - 924
The development of inhibitors toward factor VIII (FVIII) is a common and serious complication of hemophilia A (HA) therapy. Patients with hemophilia who...
recombinant factor VIII‐Fc fusion protein | hemophilia A | eloctate | factor VIII inhibitors | immune tolerance induction | Eloctate | Immune tolerance induction | Recombinant factor VIII-Fc fusion protein | Hemophilia A | Factor VIII inhibitors | recombinant factor VIII-Fc fusion protein | HEMOPHILIA-A PATIENTS | THERAPY | ONCOLOGY | PEDIATRICS | HEMATOLOGY | IMMUNOLOGICAL-TOLERANCE | Recombinant Fusion Proteins - immunology | Factor VIII - immunology | Hemophilia A - immunology | Humans | Factor VIII - genetics | Infant | Male | Receptors, Fc - immunology | Receptors, Fc - administration & dosage | Factor VIII - administration & dosage | Factor VIII - antagonists & inhibitors | Recombinant Fusion Proteins - genetics | Receptors, Fc - genetics | Blood Coagulation Factor Inhibitors - immunology | Hemophilia A - drug therapy | Desensitization, Immunologic | Recombinant Fusion Proteins - administration & dosage | Immune Tolerance - drug effects | Blood coagulation factor VIII | Hemophilia
recombinant factor VIII‐Fc fusion protein | hemophilia A | eloctate | factor VIII inhibitors | immune tolerance induction | Eloctate | Immune tolerance induction | Recombinant factor VIII-Fc fusion protein | Hemophilia A | Factor VIII inhibitors | recombinant factor VIII-Fc fusion protein | HEMOPHILIA-A PATIENTS | THERAPY | ONCOLOGY | PEDIATRICS | HEMATOLOGY | IMMUNOLOGICAL-TOLERANCE | Recombinant Fusion Proteins - immunology | Factor VIII - immunology | Hemophilia A - immunology | Humans | Factor VIII - genetics | Infant | Male | Receptors, Fc - immunology | Receptors, Fc - administration & dosage | Factor VIII - administration & dosage | Factor VIII - antagonists & inhibitors | Recombinant Fusion Proteins - genetics | Receptors, Fc - genetics | Blood Coagulation Factor Inhibitors - immunology | Hemophilia A - drug therapy | Desensitization, Immunologic | Recombinant Fusion Proteins - administration & dosage | Immune Tolerance - drug effects | Blood coagulation factor VIII | Hemophilia
Journal Article
Cardiovascular Drugs and Therapy, ISSN 0920-3206, 12/2008, Volume 22, Issue 6, pp. 437 - 442
Reperfusion of the ischemic myocardium is associated with increased inflammatory processes that can exert deleterious effects and therefore contribute to...
Remodelling | Medicine & Public Health | TNF-α | Transient ischemia | Cardiology | sTNFR-Fc | Cardiac dysfunction | ISCHEMIA/REPERFUSION INJURY | CARDIAC & CARDIOVASCULAR SYSTEMS | TNF-alpha | HEART-FAILURE | RATS | ISCHEMIA | NECROSIS-FACTOR-ALPHA | MESSENGER-RNA | ACUTE MYOCARDIAL-INFARCTION | PHARMACOLOGY & PHARMACY | EXPRESSION | Recombinant Proteins - therapeutic use | Staining and Labeling - methods | Tumor Necrosis Factor-alpha - metabolism | Rats, Wistar | Humans | Echocardiography - methods | Male | Receptors, Tumor Necrosis Factor - therapeutic use | Myocardial Reperfusion Injury - pathology | Etanercept | Time Factors | Myocardial Infarction - pathology | Immunoglobulin G - pharmacology | Myocardial Reperfusion Injury - drug therapy | Disease Models, Animal | Myocardial Infarction - diagnosis | Data Interpretation, Statistical | Immunoglobulin G - therapeutic use | Rats | Receptors, Tumor Necrosis Factor - administration & dosage | Recombinant Proteins - pharmacology | Forecasting | Immunoglobulin G - administration & dosage | Recombinant Proteins - administration & dosage | Ventricular Dysfunction, Left - physiopathology | Animals | Evans Blue | Myocardial Infarction - drug therapy | Ventricular Dysfunction, Left - drug therapy | Injections, Intravenous - methods | Hemodynamics - drug effects | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Ventricular Dysfunction, Left | Injections, Intravenous | Echocardiography | Immunoglobulin G | Recombinant Proteins | Tumor Necrosis Factor-alpha | Tissues and Organs | Life Sciences | Human health and pathology | Myocardial Infarction | Receptors, Tumor Necrosis Factor | Staining and Labeling | Myocardial Reperfusion Injury | Hemodynamics
Remodelling | Medicine & Public Health | TNF-α | Transient ischemia | Cardiology | sTNFR-Fc | Cardiac dysfunction | ISCHEMIA/REPERFUSION INJURY | CARDIAC & CARDIOVASCULAR SYSTEMS | TNF-alpha | HEART-FAILURE | RATS | ISCHEMIA | NECROSIS-FACTOR-ALPHA | MESSENGER-RNA | ACUTE MYOCARDIAL-INFARCTION | PHARMACOLOGY & PHARMACY | EXPRESSION | Recombinant Proteins - therapeutic use | Staining and Labeling - methods | Tumor Necrosis Factor-alpha - metabolism | Rats, Wistar | Humans | Echocardiography - methods | Male | Receptors, Tumor Necrosis Factor - therapeutic use | Myocardial Reperfusion Injury - pathology | Etanercept | Time Factors | Myocardial Infarction - pathology | Immunoglobulin G - pharmacology | Myocardial Reperfusion Injury - drug therapy | Disease Models, Animal | Myocardial Infarction - diagnosis | Data Interpretation, Statistical | Immunoglobulin G - therapeutic use | Rats | Receptors, Tumor Necrosis Factor - administration & dosage | Recombinant Proteins - pharmacology | Forecasting | Immunoglobulin G - administration & dosage | Recombinant Proteins - administration & dosage | Ventricular Dysfunction, Left - physiopathology | Animals | Evans Blue | Myocardial Infarction - drug therapy | Ventricular Dysfunction, Left - drug therapy | Injections, Intravenous - methods | Hemodynamics - drug effects | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Ventricular Dysfunction, Left | Injections, Intravenous | Echocardiography | Immunoglobulin G | Recombinant Proteins | Tumor Necrosis Factor-alpha | Tissues and Organs | Life Sciences | Human health and pathology | Myocardial Infarction | Receptors, Tumor Necrosis Factor | Staining and Labeling | Myocardial Reperfusion Injury | Hemodynamics
Journal Article
Journal of Neurotrauma, ISSN 0897-7151, 12/2014, Volume 31, Issue 24, pp. 1955 - 1966
Axonal growth and neurological recovery after traumatic spinal cord injury (SCI) is limited by the presence of inhibitory proteins in myelin, several of which...
Original Articles | myelin | contusion | AXONAL REGENERATION | OUTGROWTH INHIBITOR | ANTIBODY | Nogo | IDENTIFICATION | NEUROSCIENCES | translational science | MYELIN-ASSOCIATED GLYCOPROTEIN | CLINICAL NEUROLOGY | STROKE | traumatic spinal cord injury | NEURITE OUTGROWTH | GROWTH | Nogo receptor | pharmacokinetics | SOLUBLE NOGO-66 RECEPTOR | CENTRAL-NERVOUS-SYSTEM | CRITICAL CARE MEDICINE | Injections, Spinal | Spinal Cord Injuries - drug therapy | Recovery of Function - drug effects | Humans | Rats | Rats, Sprague-Dawley | Recombinant Proteins - administration & dosage | Animals | Receptors, Fc - administration & dosage | Myelin Proteins - administration & dosage | Female | Nogo Receptor 1 | Receptors, Cell Surface - administration & dosage | Neuroprotective Agents - administration & dosage | GPI-Linked Proteins - administration & dosage | Disease Models, Animal | Neurology | Care and treatment | Spinal cord injuries | Diagnosis | Analysis | Proteins | Pharmacology | Neurons | Rodents | Original
Original Articles | myelin | contusion | AXONAL REGENERATION | OUTGROWTH INHIBITOR | ANTIBODY | Nogo | IDENTIFICATION | NEUROSCIENCES | translational science | MYELIN-ASSOCIATED GLYCOPROTEIN | CLINICAL NEUROLOGY | STROKE | traumatic spinal cord injury | NEURITE OUTGROWTH | GROWTH | Nogo receptor | pharmacokinetics | SOLUBLE NOGO-66 RECEPTOR | CENTRAL-NERVOUS-SYSTEM | CRITICAL CARE MEDICINE | Injections, Spinal | Spinal Cord Injuries - drug therapy | Recovery of Function - drug effects | Humans | Rats | Rats, Sprague-Dawley | Recombinant Proteins - administration & dosage | Animals | Receptors, Fc - administration & dosage | Myelin Proteins - administration & dosage | Female | Nogo Receptor 1 | Receptors, Cell Surface - administration & dosage | Neuroprotective Agents - administration & dosage | GPI-Linked Proteins - administration & dosage | Disease Models, Animal | Neurology | Care and treatment | Spinal cord injuries | Diagnosis | Analysis | Proteins | Pharmacology | Neurons | Rodents | Original
Journal Article
The Journal of Immunology, ISSN 0022-1767, 11/2002, Volume 169, Issue 9, pp. 5171 - 5180
Many biological functions, including control of the homeostasis and maternofetal transfer of serum gamma-globulins, are mediated by the MHC class I-related...
SITE | COMPLEX | MUTAGENESIS | CRYSTAL-STRUCTURE | I-RELATED RECEPTOR | MHC | MICE | LIGAND | IMMUNOLOGY | IMMUNOGLOBULIN-G | BINDING | Surface Plasmon Resonance | Receptors, IgG - administration & dosage | Animals, Newborn - genetics | Injections, Intravenous | Immunoglobulin G - blood | Humans | Receptors, Fc - metabolism | Histocompatibility Antigens Class I | Peptide Library | Receptors, IgG - metabolism | Organ Specificity - immunology | Bacteriophage M13 - genetics | Organ Specificity - genetics | Receptors, IgG - genetics | Infant, Newborn | Receptors, IgG - blood | Mutagenesis, Site-Directed | Binding Sites, Antibody - genetics | Injections, Intramuscular | Bacteriophage M13 - immunology | Immunoglobulin G - administration & dosage | Precipitin Tests | Animals | Immunoglobulin G - genetics | Receptors, Fc - administration & dosage | Receptors, Fc - genetics | Mice | Mice, Inbred BALB C | Animals, Newborn - immunology | Receptors, Fc - blood | Hydrogen-Ion Concentration | Immunoglobulin G - metabolism
SITE | COMPLEX | MUTAGENESIS | CRYSTAL-STRUCTURE | I-RELATED RECEPTOR | MHC | MICE | LIGAND | IMMUNOLOGY | IMMUNOGLOBULIN-G | BINDING | Surface Plasmon Resonance | Receptors, IgG - administration & dosage | Animals, Newborn - genetics | Injections, Intravenous | Immunoglobulin G - blood | Humans | Receptors, Fc - metabolism | Histocompatibility Antigens Class I | Peptide Library | Receptors, IgG - metabolism | Organ Specificity - immunology | Bacteriophage M13 - genetics | Organ Specificity - genetics | Receptors, IgG - genetics | Infant, Newborn | Receptors, IgG - blood | Mutagenesis, Site-Directed | Binding Sites, Antibody - genetics | Injections, Intramuscular | Bacteriophage M13 - immunology | Immunoglobulin G - administration & dosage | Precipitin Tests | Animals | Immunoglobulin G - genetics | Receptors, Fc - administration & dosage | Receptors, Fc - genetics | Mice | Mice, Inbred BALB C | Animals, Newborn - immunology | Receptors, Fc - blood | Hydrogen-Ion Concentration | Immunoglobulin G - metabolism
Journal Article
Lancet, The, ISSN 0140-6736, 02/2008, Volume 371, Issue 9610, pp. 395 - 403
Summary Background Chronic immune thrombocytopenic purpura (ITP) is characterised by accelerated platelet destruction and decreased platelet production....
Internal Medicine | AUTOANTIBODIES | ADULT PATIENTS | IN-VITRO | AMG-531 | MEGAKARYOCYTES | CHRONIC ITP | PLATELET DESTRUCTION | SPLENECTOMY | UMCG Approved | THROMBOPOIETIN LEVELS | TGF-BETA-1 | MEDICINE, GENERAL & INTERNAL | Double-Blind Method | Drug Administration Schedule | Humans | Middle Aged | Male | Treatment Outcome | Recombinant Fusion Proteins | Thrombopoietin | Receptors, Fc - therapeutic use | Carrier Proteins - adverse effects | Splenectomy | Platelet Count | Receptors, Fc - administration & dosage | Carrier Proteins - administration & dosage | Purpura, Thrombotic Thrombocytopenic - drug therapy | Purpura, Thrombotic Thrombocytopenic - immunology | Adult | Female | Aged | Carrier Proteins - therapeutic use | Purpura, Thrombotic Thrombocytopenic - blood | Chronic Disease - drug therapy | Thrombocytopenic purpura | Drug therapy | Research | Clinical trials | Blood diseases | Medical treatment | Chronic illnesses
Internal Medicine | AUTOANTIBODIES | ADULT PATIENTS | IN-VITRO | AMG-531 | MEGAKARYOCYTES | CHRONIC ITP | PLATELET DESTRUCTION | SPLENECTOMY | UMCG Approved | THROMBOPOIETIN LEVELS | TGF-BETA-1 | MEDICINE, GENERAL & INTERNAL | Double-Blind Method | Drug Administration Schedule | Humans | Middle Aged | Male | Treatment Outcome | Recombinant Fusion Proteins | Thrombopoietin | Receptors, Fc - therapeutic use | Carrier Proteins - adverse effects | Splenectomy | Platelet Count | Receptors, Fc - administration & dosage | Carrier Proteins - administration & dosage | Purpura, Thrombotic Thrombocytopenic - drug therapy | Purpura, Thrombotic Thrombocytopenic - immunology | Adult | Female | Aged | Carrier Proteins - therapeutic use | Purpura, Thrombotic Thrombocytopenic - blood | Chronic Disease - drug therapy | Thrombocytopenic purpura | Drug therapy | Research | Clinical trials | Blood diseases | Medical treatment | Chronic illnesses
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2010, Volume 363, Issue 20, pp. 1889 - 1899
The platelet-stimulating agent romiplostim was compared with standard interventions for chronic immune thrombocytopenic purpura. Patients given romiplostim had...
MORTALITY | CONTROLLED-TRIAL | MEDICINE, GENERAL & INTERNAL | MANAGEMENT | EFFICACY | ITP | PURPURA | DOUBLE-BLIND | SPLENECTOMY | COMPLICATIONS | TERM | Glucocorticoids - therapeutic use | Recombinant Fusion Proteins - adverse effects | Humans | Middle Aged | Recombinant Fusion Proteins - therapeutic use | Male | Thrombopoietin - therapeutic use | Thrombopoietin - administration & dosage | Purpura, Thrombocytopenic, Idiopathic - drug therapy | Receptors, Fc - therapeutic use | Splenectomy | Young Adult | Injections, Subcutaneous | Treatment Failure | Aged, 80 and over | Adult | Female | Recombinant Fusion Proteins - administration & dosage | Purpura, Thrombocytopenic, Idiopathic - surgery | Platelet Count | Thrombopoietin - adverse effects | Receptors, Fc - administration & dosage | Adolescent | Intention to Treat Analysis | Quality of Life | Aged | Thrombocytopenic purpura | Medical care | Blood platelets | Drug therapy | Analysis | Quality management | Autoimmune diseases | Medical research
MORTALITY | CONTROLLED-TRIAL | MEDICINE, GENERAL & INTERNAL | MANAGEMENT | EFFICACY | ITP | PURPURA | DOUBLE-BLIND | SPLENECTOMY | COMPLICATIONS | TERM | Glucocorticoids - therapeutic use | Recombinant Fusion Proteins - adverse effects | Humans | Middle Aged | Recombinant Fusion Proteins - therapeutic use | Male | Thrombopoietin - therapeutic use | Thrombopoietin - administration & dosage | Purpura, Thrombocytopenic, Idiopathic - drug therapy | Receptors, Fc - therapeutic use | Splenectomy | Young Adult | Injections, Subcutaneous | Treatment Failure | Aged, 80 and over | Adult | Female | Recombinant Fusion Proteins - administration & dosage | Purpura, Thrombocytopenic, Idiopathic - surgery | Platelet Count | Thrombopoietin - adverse effects | Receptors, Fc - administration & dosage | Adolescent | Intention to Treat Analysis | Quality of Life | Aged | Thrombocytopenic purpura | Medical care | Blood platelets | Drug therapy | Analysis | Quality management | Autoimmune diseases | Medical research
Journal Article
British Journal of Haematology, ISSN 0007-1048, 01/2016, Volume 172, Issue 2, pp. 262 - 273
Summary In anecdotal reports, some patients with immune thrombocytopenia (ITP) maintained platelet counts after discontinuing romiplostim. Here, we examined...
thrombopoietin receptor agonist | romiplostim | platelet response | immune thrombocytopenia | remission | Romiplostim | Remission | Thrombopoietin receptor agonist | Immune thrombocytopenia | Platelet response | PURPURA ITP | EFFICACY | ADULTS | THROMBOPOIETIN-RECEPTOR AGONISTS | HIGH-DOSE DEXAMETHASONE | THERAPY | RITUXIMAB | 2ND-LINE TREATMENT | RETROSPECTIVE ANALYSIS | HEMATOLOGY | LONG-TERM TREATMENT | Prospective Studies | Recombinant Fusion Proteins - adverse effects | Humans | Middle Aged | Recombinant Fusion Proteins - therapeutic use | Male | Thrombopoietin - therapeutic use | Thrombopoietin - administration & dosage | Receptors, Fc - therapeutic use | Thrombocytopenia - drug therapy | Adult | Female | Blood Platelets - drug effects | Autoimmune Diseases - drug therapy | Recombinant Fusion Proteins - administration & dosage | Drug Administration Schedule | Kaplan-Meier Estimate | Treatment Outcome | Remission Induction | Thrombocytopenia - blood | Autoimmune Diseases - blood | Receptors, Thrombopoietin - agonists | Platelet Count | Thrombopoietin - adverse effects | Receptors, Fc - administration & dosage | Thrombocytopenia | Immune response
thrombopoietin receptor agonist | romiplostim | platelet response | immune thrombocytopenia | remission | Romiplostim | Remission | Thrombopoietin receptor agonist | Immune thrombocytopenia | Platelet response | PURPURA ITP | EFFICACY | ADULTS | THROMBOPOIETIN-RECEPTOR AGONISTS | HIGH-DOSE DEXAMETHASONE | THERAPY | RITUXIMAB | 2ND-LINE TREATMENT | RETROSPECTIVE ANALYSIS | HEMATOLOGY | LONG-TERM TREATMENT | Prospective Studies | Recombinant Fusion Proteins - adverse effects | Humans | Middle Aged | Recombinant Fusion Proteins - therapeutic use | Male | Thrombopoietin - therapeutic use | Thrombopoietin - administration & dosage | Receptors, Fc - therapeutic use | Thrombocytopenia - drug therapy | Adult | Female | Blood Platelets - drug effects | Autoimmune Diseases - drug therapy | Recombinant Fusion Proteins - administration & dosage | Drug Administration Schedule | Kaplan-Meier Estimate | Treatment Outcome | Remission Induction | Thrombocytopenia - blood | Autoimmune Diseases - blood | Receptors, Thrombopoietin - agonists | Platelet Count | Thrombopoietin - adverse effects | Receptors, Fc - administration & dosage | Thrombocytopenia | Immune response
Journal Article
Blood, ISSN 0006-4971, 03/2009, Volume 113, Issue 10, pp. 2161 - 2171
Chronic immune thrombocytopenic purpura (ITP) is characterized by low platelet counts and mucocutaneous bleeding. In previous studies romiplostim (AMG531), a...
AUTOIMMUNE THROMBOCYTOPENIA | ADULT PATIENTS | INTRAVENOUS GAMMA-GLOBULIN | IN-VITRO | PURPURA | AMG-531 | BONE-MARROW | SPLENECTOMY | PLATELET PRODUCTION | HEMATOLOGY | THROMBOPOIETIN LEVELS | Humans | Middle Aged | Male | Recombinant Fusion Proteins | Thrombopoietin | Purpura, Thrombocytopenic, Idiopathic - drug therapy | Carrier Proteins - adverse effects | Platelet Count | Receptors, Fc - administration & dosage | Carrier Proteins - administration & dosage | Female | Blood Platelets - drug effects | Thrombopoiesis - drug effects
AUTOIMMUNE THROMBOCYTOPENIA | ADULT PATIENTS | INTRAVENOUS GAMMA-GLOBULIN | IN-VITRO | PURPURA | AMG-531 | BONE-MARROW | SPLENECTOMY | PLATELET PRODUCTION | HEMATOLOGY | THROMBOPOIETIN LEVELS | Humans | Middle Aged | Male | Recombinant Fusion Proteins | Thrombopoietin | Purpura, Thrombocytopenic, Idiopathic - drug therapy | Carrier Proteins - adverse effects | Platelet Count | Receptors, Fc - administration & dosage | Carrier Proteins - administration & dosage | Female | Blood Platelets - drug effects | Thrombopoiesis - drug effects
Journal Article