The New England Journal of Medicine, ISSN 0028-4793, 08/2013, Volume 369, Issue 7, pp. 630 - 639
In this phase 2b study, an interferon-free regimen consisting of the combination of a protease inhibitor (faldaprevir), a nonnucleoside polymerase inhibitor...
PROTEASE INHIBITOR | GENOTYPE-1-INFECTED SUBJECTS | ANTIVIRAL AGENTS | MEDICINE, GENERAL & INTERNAL | TELAPREVIR | C VIRUS-INFECTION | INTERFERON-FREE REGIMEN | INHIBITOR BI 207127 | RIBAVIRIN | COMBINATION | HEPATITIS-C | Enzyme Inhibitors - adverse effects | DNA-Directed RNA Polymerases - antagonists & inhibitors | Antiviral Agents - therapeutic use | Humans | Middle Aged | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Genotype | Male | Thiazoles - therapeutic use | Hepatitis C, Chronic - drug therapy | Oligopeptides - adverse effects | Enzyme Inhibitors - therapeutic use | Thiazoles - adverse effects | Viral Load | Oligopeptides - therapeutic use | Antiviral Agents - adverse effects | Protease Inhibitors - adverse effects | Adult | Female | Hepatitis C, Chronic - genetics | Protease Inhibitors - therapeutic use | Clinical trials | Antiviral agents | Research | Hepatitis C | Drug therapy | Photosensitivity | Diarrhea | Chronic infection | Nausea | Proteinase inhibitors | Patients | Ribavirin | Hepatitis | Vomiting | Human immunodeficiency virus--HIV | Interferon | Drug dosages | Genotypes
PROTEASE INHIBITOR | GENOTYPE-1-INFECTED SUBJECTS | ANTIVIRAL AGENTS | MEDICINE, GENERAL & INTERNAL | TELAPREVIR | C VIRUS-INFECTION | INTERFERON-FREE REGIMEN | INHIBITOR BI 207127 | RIBAVIRIN | COMBINATION | HEPATITIS-C | Enzyme Inhibitors - adverse effects | DNA-Directed RNA Polymerases - antagonists & inhibitors | Antiviral Agents - therapeutic use | Humans | Middle Aged | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Genotype | Male | Thiazoles - therapeutic use | Hepatitis C, Chronic - drug therapy | Oligopeptides - adverse effects | Enzyme Inhibitors - therapeutic use | Thiazoles - adverse effects | Viral Load | Oligopeptides - therapeutic use | Antiviral Agents - adverse effects | Protease Inhibitors - adverse effects | Adult | Female | Hepatitis C, Chronic - genetics | Protease Inhibitors - therapeutic use | Clinical trials | Antiviral agents | Research | Hepatitis C | Drug therapy | Photosensitivity | Diarrhea | Chronic infection | Nausea | Proteinase inhibitors | Patients | Ribavirin | Hepatitis | Vomiting | Human immunodeficiency virus--HIV | Interferon | Drug dosages | Genotypes
Journal Article
JAMA, ISSN 0098-7484, 11/2011, Volume 306, Issue 19, pp. 2137 - 2144
CONTEXT Recurrent stroke prevention guidelines suggest that larger reductions in systolic blood pressure (SBP) are positively associated with a greater...
TELMISARTAN | MEDICINE, GENERAL & INTERNAL | CARDIOVASCULAR OUTCOMES | TRANSIENT ISCHEMIC ATTACK | EXTENDED-RELEASE DIPYRIDAMOLE | COMBINATION | HEALTH-CARE PROFESSIONALS | PROGNOSTIC VALUE | ASSOCIATION | HYPERTENSIVE PATIENTS | SECONDARY PREVENTION | Blood Pressure | Recurrence | Benzoates - therapeutic use | Diastole | Follow-Up Studies | Ticlopidine - therapeutic use | Humans | Middle Aged | Male | Reference Values | Risk | Systole | Vascular Diseases - mortality | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Female | Aspirin - therapeutic use | Stroke - mortality | Benzimidazoles - therapeutic use | Stroke - prevention & control | Brain Ischemia - prevention & control | Ticlopidine - analogs & derivatives | Randomized Controlled Trials as Topic | Myocardial Infarction | Platelet Aggregation Inhibitors | Aged | Brain Ischemia - mortality | Dipyridamole - administration & dosage | Measurement | Stroke (Disease) | Causes of | Blood pressure | Methods | Medical records | Medical research | Stroke
TELMISARTAN | MEDICINE, GENERAL & INTERNAL | CARDIOVASCULAR OUTCOMES | TRANSIENT ISCHEMIC ATTACK | EXTENDED-RELEASE DIPYRIDAMOLE | COMBINATION | HEALTH-CARE PROFESSIONALS | PROGNOSTIC VALUE | ASSOCIATION | HYPERTENSIVE PATIENTS | SECONDARY PREVENTION | Blood Pressure | Recurrence | Benzoates - therapeutic use | Diastole | Follow-Up Studies | Ticlopidine - therapeutic use | Humans | Middle Aged | Male | Reference Values | Risk | Systole | Vascular Diseases - mortality | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Female | Aspirin - therapeutic use | Stroke - mortality | Benzimidazoles - therapeutic use | Stroke - prevention & control | Brain Ischemia - prevention & control | Ticlopidine - analogs & derivatives | Randomized Controlled Trials as Topic | Myocardial Infarction | Platelet Aggregation Inhibitors | Aged | Brain Ischemia - mortality | Dipyridamole - administration & dosage | Measurement | Stroke (Disease) | Causes of | Blood pressure | Methods | Medical records | Medical research | Stroke
Journal Article
Breast Cancer Research and Treatment, ISSN 0167-6806, 6/2012, Volume 133, Issue 3, pp. 1057 - 1065
Afatinib is an oral, ErbB family blocker, which covalently binds and irreversibly blocks all kinase-competent ErbB family members. This phase II, open-label,...
Human epidermal growth factor receptor | Medicine & Public Health | ErbB2 | ErbB1 | Oncology | Breast cancer | Second-generation small molecule kinase inhibitors | Trastuzumab | LAPATINIB | GROWTH-FACTOR RECEPTOR | ONCOLOGY | EGFR/HER2 INHIBITOR | TYROSINE KINASE | RESISTANCE | Antibodies, Monoclonal, Humanized - therapeutic use | Humans | Middle Aged | Receptor, ErbB-2 - metabolism | Treatment Outcome | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - administration & dosage | Breast Neoplasms - drug therapy | Disease Progression | Breast Neoplasms - metabolism | Neoplasm Metastasis | Antineoplastic Agents - adverse effects | Breast Neoplasms - pathology | Quinazolines - therapeutic use | Quinazolines - adverse effects | Aged, 80 and over | Adult | Breast Neoplasms - mortality | Female | Quinazolines - administration & dosage | Aged | Receptor, ErbB-2 - antagonists & inhibitors | Antimitotic agents | Medical research | Care and treatment | Cancer patients | Chemotherapy | Epidermal growth factor | Medicine, Experimental | Metastasis | Antineoplastic agents | Cancer | Clinical Trial
Human epidermal growth factor receptor | Medicine & Public Health | ErbB2 | ErbB1 | Oncology | Breast cancer | Second-generation small molecule kinase inhibitors | Trastuzumab | LAPATINIB | GROWTH-FACTOR RECEPTOR | ONCOLOGY | EGFR/HER2 INHIBITOR | TYROSINE KINASE | RESISTANCE | Antibodies, Monoclonal, Humanized - therapeutic use | Humans | Middle Aged | Receptor, ErbB-2 - metabolism | Treatment Outcome | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - administration & dosage | Breast Neoplasms - drug therapy | Disease Progression | Breast Neoplasms - metabolism | Neoplasm Metastasis | Antineoplastic Agents - adverse effects | Breast Neoplasms - pathology | Quinazolines - therapeutic use | Quinazolines - adverse effects | Aged, 80 and over | Adult | Breast Neoplasms - mortality | Female | Quinazolines - administration & dosage | Aged | Receptor, ErbB-2 - antagonists & inhibitors | Antimitotic agents | Medical research | Care and treatment | Cancer patients | Chemotherapy | Epidermal growth factor | Medicine, Experimental | Metastasis | Antineoplastic agents | Cancer | Clinical Trial
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2019, Volume 78, Issue 6, pp. 754 - 760
ObjectiveTo evaluate the safety, efficacy and therapeutic mechanism of BI 655064, an antagonistic anti-CD40 monoclonal antibody, in patients with rheumatoid...
SYSTEMIC-LUPUS-ERYTHEMATOSUS | INCREASED EXPRESSION | PHARMACOKINETICS | EFFICACY | SAFETY | INADEQUATE RESPONSE | CD40 LIGAND | RHEUMATOLOGY | INHIBITOR | T-CELLS | DISEASE-ACTIVITY | B-cells | Rheumatoid Arthritis | 1506 | autoantibodies | 2311
SYSTEMIC-LUPUS-ERYTHEMATOSUS | INCREASED EXPRESSION | PHARMACOKINETICS | EFFICACY | SAFETY | INADEQUATE RESPONSE | CD40 LIGAND | RHEUMATOLOGY | INHIBITOR | T-CELLS | DISEASE-ACTIVITY | B-cells | Rheumatoid Arthritis | 1506 | autoantibodies | 2311
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 06/2019, Volume 143, Issue 6, pp. 2158 - 2169
IL-23 contributes to the activation, maintenance, and proliferation of T 17 cells and plays a major role in psoriasis pathophysiology. IL-23p19 inhibition with...
ustekinumab | psoriasis | biomarkers | IL-17 | Risankizumab | IL-23 | IL-12 | Immunohistochemistry | Skin | Psoriasis | Dendritic cells | Analysis | Cell proliferation | Genes | Helper cells | Hispanic Americans | Interleukin 23 | Lymphocytes T | Gene sequencing | Histopathology | Lymphocytes | Skin diseases | Lesions | CD11c antigen | Cytokines | Lipocalin | Glycoprotein | Keratinocytes | Interleukin 12 | CD3 antigen | Ribonucleic acid--RNA | Gene expression | Patients | Studies | Monocytes | Biopsy | Biomarkers | Sampling methods
ustekinumab | psoriasis | biomarkers | IL-17 | Risankizumab | IL-23 | IL-12 | Immunohistochemistry | Skin | Psoriasis | Dendritic cells | Analysis | Cell proliferation | Genes | Helper cells | Hispanic Americans | Interleukin 23 | Lymphocytes T | Gene sequencing | Histopathology | Lymphocytes | Skin diseases | Lesions | CD11c antigen | Cytokines | Lipocalin | Glycoprotein | Keratinocytes | Interleukin 12 | CD3 antigen | Ribonucleic acid--RNA | Gene expression | Patients | Studies | Monocytes | Biopsy | Biomarkers | Sampling methods
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, p. e0160668
Background & Aim The resistance profile of anti-hepatitis C virus (HCV) agents used in combination is important to guide optimal treatment regimens. We...
PRECLINICAL CHARACTERIZATION | THERAPY | BI 207127 | VARIANTS | SOFOSBUVIR | MULTIDISCIPLINARY SCIENCES | INFECTION | RIBAVIRIN | INHIBITOR | HEPATITIS-C | BMS-791325 | Acrylates - therapeutic use | Humans | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Thiazoles - therapeutic use | Hepacivirus - metabolism | Oligopeptides - therapeutic use | Clinical Trials, Phase III as Topic | Protease Inhibitors - therapeutic use | Benzimidazoles - therapeutic use | Hepacivirus - drug effects | Antiviral Agents - therapeutic use | Carrier Proteins - antagonists & inhibitors | Viral Nonstructural Proteins - genetics | Treatment Outcome | Hepatitis C, Chronic - drug therapy | Mutation - genetics | Polymorphism, Genetic - drug effects | Carrier Proteins - genetics | Carrier Proteins - metabolism | Drug Resistance, Viral - drug effects | Polymorphism, Genetic - genetics | Viral Nonstructural Proteins - metabolism | Hepatitis C, Chronic - genetics | Viral Nonstructural Proteins - antagonists & inhibitors | Clinical Trials, Phase I as Topic | Amino Acid Substitution | Clinical Trials, Phase II as Topic | Antiviral agents | Complications and side effects | Drug resistance in microorganisms | Proteases | Physiological aspects | Dosage and administration | Genetic aspects | Research | Hepatitis C | Drug therapy | Clinical trials | Amino acids | Viruses | Infections | Ribavirin | Disease resistance | Hepatitis | Genotype & phenotype | Consolidation | Protease | Gastroenterology | Genotypes | Alanine | RNA polymerase | Patients | RNA-directed RNA polymerase | Studies | Polymerase | Inhibitors | Acids | Interferon | Hepatitis C virus | Binding sites | Polymorphism | Pharmaceuticals
PRECLINICAL CHARACTERIZATION | THERAPY | BI 207127 | VARIANTS | SOFOSBUVIR | MULTIDISCIPLINARY SCIENCES | INFECTION | RIBAVIRIN | INHIBITOR | HEPATITIS-C | BMS-791325 | Acrylates - therapeutic use | Humans | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Thiazoles - therapeutic use | Hepacivirus - metabolism | Oligopeptides - therapeutic use | Clinical Trials, Phase III as Topic | Protease Inhibitors - therapeutic use | Benzimidazoles - therapeutic use | Hepacivirus - drug effects | Antiviral Agents - therapeutic use | Carrier Proteins - antagonists & inhibitors | Viral Nonstructural Proteins - genetics | Treatment Outcome | Hepatitis C, Chronic - drug therapy | Mutation - genetics | Polymorphism, Genetic - drug effects | Carrier Proteins - genetics | Carrier Proteins - metabolism | Drug Resistance, Viral - drug effects | Polymorphism, Genetic - genetics | Viral Nonstructural Proteins - metabolism | Hepatitis C, Chronic - genetics | Viral Nonstructural Proteins - antagonists & inhibitors | Clinical Trials, Phase I as Topic | Amino Acid Substitution | Clinical Trials, Phase II as Topic | Antiviral agents | Complications and side effects | Drug resistance in microorganisms | Proteases | Physiological aspects | Dosage and administration | Genetic aspects | Research | Hepatitis C | Drug therapy | Clinical trials | Amino acids | Viruses | Infections | Ribavirin | Disease resistance | Hepatitis | Genotype & phenotype | Consolidation | Protease | Gastroenterology | Genotypes | Alanine | RNA polymerase | Patients | RNA-directed RNA polymerase | Studies | Polymerase | Inhibitors | Acids | Interferon | Hepatitis C virus | Binding sites | Polymorphism | Pharmaceuticals
Journal Article
International Journal of Stroke, ISSN 1747-4930, 10/2014, Volume 9, Issue 7, pp. 873 - 878
Background Risk profiles for stroke recurrence are poorly characterized. Aims We determined the variation in the risk and type of recurrent stroke among index...
predictors | recurrence | ischemic | risk factors | stroke | Recurrence | Stroke | Ischemic | Risk factors | Predictors | EVENTS | ASPIRIN | CLOPIDOGREL | RISK-FACTOR | CEREBRAL MICROBLEEDS | INTRACEREBRAL HEMORRHAGE | ATTACK | PERIPHERAL VASCULAR DISEASE | LACUNAR STROKE | Brain Ischemia - epidemiology | Stroke - prevention & control | Brain Ischemia - classification | Humans | Kaplan-Meier Estimate | Male | Risk | Brain Ischemia - prevention & control | Stroke - drug therapy | Secondary Prevention - methods | Stroke - classification | Brain Ischemia - drug therapy | Female | Stroke - epidemiology | Aged | Hypertension | Care and treatment | Aspirin | Relapse | Atrial fibrillation | Anticoagulants (Medicine) | Diseases | Stroke (Disease) | Ischemia | Analysis | Hypoglycemic agents | Stroke patients | Smoking
predictors | recurrence | ischemic | risk factors | stroke | Recurrence | Stroke | Ischemic | Risk factors | Predictors | EVENTS | ASPIRIN | CLOPIDOGREL | RISK-FACTOR | CEREBRAL MICROBLEEDS | INTRACEREBRAL HEMORRHAGE | ATTACK | PERIPHERAL VASCULAR DISEASE | LACUNAR STROKE | Brain Ischemia - epidemiology | Stroke - prevention & control | Brain Ischemia - classification | Humans | Kaplan-Meier Estimate | Male | Risk | Brain Ischemia - prevention & control | Stroke - drug therapy | Secondary Prevention - methods | Stroke - classification | Brain Ischemia - drug therapy | Female | Stroke - epidemiology | Aged | Hypertension | Care and treatment | Aspirin | Relapse | Atrial fibrillation | Anticoagulants (Medicine) | Diseases | Stroke (Disease) | Ischemia | Analysis | Hypoglycemic agents | Stroke patients | Smoking
Journal Article
Stroke, ISSN 0039-2499, 05/2013, Volume 44, Issue 5, pp. 1238 - 1243
Background and Purpose-Chronic pain syndromes are reported to be common after stroke, but most previous epidemiological studies have generally included small...
epidemiology | pain | ischemic stroke | MEDICAL COMPLICATIONS | POPULATION | RISK-FACTORS | PREVALENCE | CLINICAL NEUROLOGY | LONG-TERM PAIN | PERIPHERAL VASCULAR DISEASE | QUALITY-OF-LIFE | RECURRENT STROKE | EXTENDED-RELEASE DIPYRIDAMOLE | SHOULDER PAIN | CENTRAL POSTSTROKE PAIN | Brain Ischemia - complications | Brain Ischemia - epidemiology | Severity of Illness Index | Follow-Up Studies | Stroke - psychology | Humans | Middle Aged | Risk Factors | Stroke - complications | Male | Neuropsychological Tests | Chronic Pain - epidemiology | Cognition Disorders - etiology | Brain Ischemia - psychology | Aged, 80 and over | Female | Stroke - epidemiology | Aged | Pain Measurement | Chronic Pain - etiology | Cognition Disorders - epidemiology
epidemiology | pain | ischemic stroke | MEDICAL COMPLICATIONS | POPULATION | RISK-FACTORS | PREVALENCE | CLINICAL NEUROLOGY | LONG-TERM PAIN | PERIPHERAL VASCULAR DISEASE | QUALITY-OF-LIFE | RECURRENT STROKE | EXTENDED-RELEASE DIPYRIDAMOLE | SHOULDER PAIN | CENTRAL POSTSTROKE PAIN | Brain Ischemia - complications | Brain Ischemia - epidemiology | Severity of Illness Index | Follow-Up Studies | Stroke - psychology | Humans | Middle Aged | Risk Factors | Stroke - complications | Male | Neuropsychological Tests | Chronic Pain - epidemiology | Cognition Disorders - etiology | Brain Ischemia - psychology | Aged, 80 and over | Female | Stroke - epidemiology | Aged | Pain Measurement | Chronic Pain - etiology | Cognition Disorders - epidemiology
Journal Article
RESPIRATORY RESEARCH, ISSN 1465-993X, 10/2019, Volume 20, Issue 1, pp. 1 - 13
Background: Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease for which diagnosis and management remain challenging. Defining the circulating...
LUNG | DIAGNOSIS | Observational study | Interstitial lung diseases | RESPIRATORY SYSTEM | DISEASE | TISSUE | Proteome | Registries | SARCOIDOSIS | Research
LUNG | DIAGNOSIS | Observational study | Interstitial lung diseases | RESPIRATORY SYSTEM | DISEASE | TISSUE | Proteome | Registries | SARCOIDOSIS | Research
Journal Article
Stroke, ISSN 0039-2499, 12/2011, Volume 42, Issue 12, pp. 3397 - 3402
Background and Purpose-Although obesity is an established risk factor for the occurrence of a primary stroke, little is known about the impact of baseline...
Myocardial infarction | Body mass index | Obesity | Paradox | Prognosis | Recurrent stroke | Outcomes | Vascular death | Overweight | METABOLIC SYNDROME | vascular death | body mass index | myocardial infarction | PREVENTION | prognosis | CLINICAL NEUROLOGY | TELMISARTAN | IMPACT | CLOPIDOGREL | recurrent stroke | outcomes | paradox | BODY-MASS INDEX | PERIPHERAL VASCULAR DISEASE | EXTENDED-RELEASE DIPYRIDAMOLE | OF-NEUROLOGY AFFIRMS | WEIGHT | overweight | obesity | Brain Ischemia - complications | Brain Ischemia - epidemiology | Cardiovascular Diseases - etiology | Recurrence | Obesity - complications | Humans | Middle Aged | Risk Factors | Stroke - complications | Male | Risk | Obesity - epidemiology | Cardiovascular Diseases - epidemiology | Female | Stroke - epidemiology | Aged | Databases, Factual
Myocardial infarction | Body mass index | Obesity | Paradox | Prognosis | Recurrent stroke | Outcomes | Vascular death | Overweight | METABOLIC SYNDROME | vascular death | body mass index | myocardial infarction | PREVENTION | prognosis | CLINICAL NEUROLOGY | TELMISARTAN | IMPACT | CLOPIDOGREL | recurrent stroke | outcomes | paradox | BODY-MASS INDEX | PERIPHERAL VASCULAR DISEASE | EXTENDED-RELEASE DIPYRIDAMOLE | OF-NEUROLOGY AFFIRMS | WEIGHT | overweight | obesity | Brain Ischemia - complications | Brain Ischemia - epidemiology | Cardiovascular Diseases - etiology | Recurrence | Obesity - complications | Humans | Middle Aged | Risk Factors | Stroke - complications | Male | Risk | Obesity - epidemiology | Cardiovascular Diseases - epidemiology | Female | Stroke - epidemiology | Aged | Databases, Factual
Journal Article
Cancer, ISSN 0008-543X, 04/2014, Volume 120, Issue 7, pp. 976 - 982
BACKGROUND Polo‐like kinases (Plks) control multiple steps during the cell cycle, and Plk1 is overexpressed in urothelial cancer (UC). Volasertib (BI 6727), a...
phase 2 trial | volasertib | urothelial cancer | polo‐like kinase inhibitor | polo-like kinase inhibitor | Protein Kinase Inhibitors - pharmacokinetics | Urologic Neoplasms - metabolism | Pteridines - therapeutic use | Humans | Middle Aged | Male | Pteridines - pharmacokinetics | Treatment Outcome | Antineoplastic Agents - therapeutic use | Disease-Free Survival | Urologic Neoplasms - pathology | Neoplasm Metastasis | Urologic Neoplasms - drug therapy | Protein Kinase Inhibitors - therapeutic use | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Aged, 80 and over | Female | Aged | Antineoplastic Agents - pharmacokinetics | Urologic Neoplasms - enzymology | Evaluation | Influence | Phosphotransferases | Index Medicus | Abridged Index Medicus
phase 2 trial | volasertib | urothelial cancer | polo‐like kinase inhibitor | polo-like kinase inhibitor | Protein Kinase Inhibitors - pharmacokinetics | Urologic Neoplasms - metabolism | Pteridines - therapeutic use | Humans | Middle Aged | Male | Pteridines - pharmacokinetics | Treatment Outcome | Antineoplastic Agents - therapeutic use | Disease-Free Survival | Urologic Neoplasms - pathology | Neoplasm Metastasis | Urologic Neoplasms - drug therapy | Protein Kinase Inhibitors - therapeutic use | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Aged, 80 and over | Female | Aged | Antineoplastic Agents - pharmacokinetics | Urologic Neoplasms - enzymology | Evaluation | Influence | Phosphotransferases | Index Medicus | Abridged Index Medicus
Journal Article
Journal of Crohn's & colitis, ISSN 1873-9946, 2018, Volume 12, Issue 10, pp. 1170 - 1179
Background and Aims: We aimed to investigate the underlying mechanism of action of risankizumab, a monoclonal antibody targeting the IL-23 p19 subunit,...
Biomarkers | Clinical trials | Endoscopy | INFLAMMATORY-BOWEL-DISEASE | biomarkers | DOUBLE-BLIND | endoscopy | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | TH17 CELLS | Biopsy - methods | Ileum - pathology | Interleukin-23 Subunit p19 - antagonists & inhibitors | Gene Expression - drug effects | Humans | Immunosuppressive Agents - pharmacokinetics | Middle Aged | Colon - drug effects | Interleukin-17 - immunology | Colon - immunology | Male | Drug Monitoring - methods | Ileum - immunology | Ileum - drug effects | Crohn Disease - diagnosis | Adult | Female | Immunosuppressive Agents - administration & dosage | Double-Blind Method | Colon - pathology | Antibodies, Monoclonal - pharmacokinetics | Gene Expression Profiling - methods | Crohn Disease - immunology | Remission Induction | Endoscopy, Digestive System - methods | Monitoring, Immunologic - methods | Patient Acuity | Antibodies, Monoclonal - administration & dosage | Crohn Disease - drug therapy | Interleukin-23 Subunit p19 - immunology
Biomarkers | Clinical trials | Endoscopy | INFLAMMATORY-BOWEL-DISEASE | biomarkers | DOUBLE-BLIND | endoscopy | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | TH17 CELLS | Biopsy - methods | Ileum - pathology | Interleukin-23 Subunit p19 - antagonists & inhibitors | Gene Expression - drug effects | Humans | Immunosuppressive Agents - pharmacokinetics | Middle Aged | Colon - drug effects | Interleukin-17 - immunology | Colon - immunology | Male | Drug Monitoring - methods | Ileum - immunology | Ileum - drug effects | Crohn Disease - diagnosis | Adult | Female | Immunosuppressive Agents - administration & dosage | Double-Blind Method | Colon - pathology | Antibodies, Monoclonal - pharmacokinetics | Gene Expression Profiling - methods | Crohn Disease - immunology | Remission Induction | Endoscopy, Digestive System - methods | Monitoring, Immunologic - methods | Patient Acuity | Antibodies, Monoclonal - administration & dosage | Crohn Disease - drug therapy | Interleukin-23 Subunit p19 - immunology
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 2019
Journal Article
AIDS, ISSN 0269-9370, 03/2015, Volume 29, Issue 5, pp. 571 - 581
OBJECTIVE:Faldaprevir is a potent, once-daily hepatitis C virus (HCV) NS3/4A protease inhibitor. STARTVerso4 assessed the efficacy and safety of faldaprevir...
SVR12 | faldaprevir | NS3/4A protease inhibitor | HIV | hepatitis C virus genotype 1 | Recombinant Proteins - therapeutic use | Viremia - diagnosis | Anti-Retroviral Agents - therapeutic use | Antiviral Agents - therapeutic use | Humans | Middle Aged | Ribavirin - therapeutic use | Interferon-alpha - therapeutic use | Treatment Outcome | Thiazoles - therapeutic use | Hepatitis C, Chronic - drug therapy | Polyethylene Glycols - therapeutic use | Viral Load | Oligopeptides - therapeutic use | Young Adult | Drug Therapy, Combination - methods | Adolescent | HIV Infections - complications | Adult | Aged
SVR12 | faldaprevir | NS3/4A protease inhibitor | HIV | hepatitis C virus genotype 1 | Recombinant Proteins - therapeutic use | Viremia - diagnosis | Anti-Retroviral Agents - therapeutic use | Antiviral Agents - therapeutic use | Humans | Middle Aged | Ribavirin - therapeutic use | Interferon-alpha - therapeutic use | Treatment Outcome | Thiazoles - therapeutic use | Hepatitis C, Chronic - drug therapy | Polyethylene Glycols - therapeutic use | Viral Load | Oligopeptides - therapeutic use | Young Adult | Drug Therapy, Combination - methods | Adolescent | HIV Infections - complications | Adult | Aged
Journal Article
The Journal of Clinical Pharmacology, ISSN 0091-2700, 07/2011, Volume 51, Issue 7, pp. 1061 - 1070
The objective of this investigation was to evaluate the pharmacokinetic interaction of lopinavir/ritonavir (LPV/r) with BILR 355. In group A, 26 healthy...
lopinavir | HIV | drug‐drug interaction | BILR 355 | ritonavir | nonnucleoside reverse transcriptase inhibitor | P‐glycoprotein | protease inhibitor (PI) | P-glycoprotein | drug-drug interaction | IMMUNODEFICIENCY-VIRUS-INFECTION | SAFETY | HIV-1-INFECTED PATIENTS | PROTEASE INHIBITOR | HEPATIC CYP3A | HIV-INFECTION | THERAPY | RESISTANCE | ANTIVIRAL ACTIVITY | PHARMACOLOGY & PHARMACY | LOPINAVIR/RITONAVIR | Reverse Transcriptase Inhibitors - blood | Humans | Middle Aged | Half-Life | Pyridines - pharmacokinetics | Biological Availability | Male | Reverse Transcriptase Inhibitors - adverse effects | Young Adult | Pyridines - adverse effects | Reverse Transcriptase Inhibitors - pharmacokinetics | Drug Interactions | Ritonavir - adverse effects | HIV Protease Inhibitors - pharmacokinetics | Adult | Female | Drug Therapy, Combination | HIV Protease Inhibitors - adverse effects | HIV Protease Inhibitors - blood | Azepines - adverse effects | Ritonavir - administration & dosage | Ritonavir - blood | Lopinavir | Pyrimidinones - adverse effects | Azepines - blood | HIV Protease Inhibitors - administration & dosage | Pyridines - blood | Pyrimidinones - pharmacokinetics | Ritonavir - pharmacokinetics | Pyrimidinones - blood | Azepines - pharmacokinetics | Pyrimidinones - administration & dosage | Ritonavir | Drug interactions | Physiological aspects | Dosage and administration | Reverse transcriptase inhibitors | Research | Bioavailability | Protease inhibitors | Drug dosages | Human immunodeficiency virus--HIV | Index Medicus
lopinavir | HIV | drug‐drug interaction | BILR 355 | ritonavir | nonnucleoside reverse transcriptase inhibitor | P‐glycoprotein | protease inhibitor (PI) | P-glycoprotein | drug-drug interaction | IMMUNODEFICIENCY-VIRUS-INFECTION | SAFETY | HIV-1-INFECTED PATIENTS | PROTEASE INHIBITOR | HEPATIC CYP3A | HIV-INFECTION | THERAPY | RESISTANCE | ANTIVIRAL ACTIVITY | PHARMACOLOGY & PHARMACY | LOPINAVIR/RITONAVIR | Reverse Transcriptase Inhibitors - blood | Humans | Middle Aged | Half-Life | Pyridines - pharmacokinetics | Biological Availability | Male | Reverse Transcriptase Inhibitors - adverse effects | Young Adult | Pyridines - adverse effects | Reverse Transcriptase Inhibitors - pharmacokinetics | Drug Interactions | Ritonavir - adverse effects | HIV Protease Inhibitors - pharmacokinetics | Adult | Female | Drug Therapy, Combination | HIV Protease Inhibitors - adverse effects | HIV Protease Inhibitors - blood | Azepines - adverse effects | Ritonavir - administration & dosage | Ritonavir - blood | Lopinavir | Pyrimidinones - adverse effects | Azepines - blood | HIV Protease Inhibitors - administration & dosage | Pyridines - blood | Pyrimidinones - pharmacokinetics | Ritonavir - pharmacokinetics | Pyrimidinones - blood | Azepines - pharmacokinetics | Pyrimidinones - administration & dosage | Ritonavir | Drug interactions | Physiological aspects | Dosage and administration | Reverse transcriptase inhibitors | Research | Bioavailability | Protease inhibitors | Drug dosages | Human immunodeficiency virus--HIV | Index Medicus
Journal Article