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Keyphrases
Hepatocellular Carcinoma
100%
Phase 1 Trial
100%
Sorafenib
100%
Expansion Cohort
100%
Navitoclax
100%
Refractory Solid Tumors
100%
Dose Level
63%
Dose Escalation
27%
Maximum Tolerated Dose
18%
Twice Daily
18%
Tumor Angiogenesis
9%
Apoptosis
9%
Inhibit Tumor
9%
Stable Disease
9%
Dose-limiting Toxicity
9%
Rash
9%
Thrombocytopenia
9%
Clinical Benefit
9%
Oral Administration
9%
Complete Response
9%
Advanced Hepatocellular Carcinoma
9%
Progressive Disease
9%
Partial Response
9%
Evaluation Program
9%
Apoptosis Induction
9%
National Cancer Institute
9%
Cancer Therapy
9%
Pharmacokinetic Study
9%
2-cycles
9%
Bcl-2 Family Proteins
9%
High Affinity
9%
Pharmacodynamic Study
9%
Toxicity Grades
9%
Hypertension
9%
Drug Interactions
9%
Clinical Trial Data
9%
Aspartate Aminotransferase
9%
Pro-survival
9%
Promote Apoptosis
9%
Further Development
9%
Therapy Evaluation
9%
One Dose
9%
Two-dose
9%
Continual Reassessment Method
9%
ABT-263
9%
Aminotransferase Elevation
9%
CRADA
9%
Bcl-2 Homology 3 Mimetics
9%
Oral multikinase Inhibitors
9%
Medicine and Dentistry
Solid Malignant Neoplasm
100%
Hepatocellular Carcinoma
100%
Sorafenib
100%
Navitoclax
100%
Programmed Cell Death
27%
Oral
18%
Malignant Neoplasm
9%
Diseases
9%
Clinical Trial
9%
Oral Drug Administration
9%
Cancer Therapy
9%
Progressive Disease
9%
Thrombocytopenia
9%
Pharmacokinetic
9%
Tumor Angiogenesis
9%
Pharmacodynamics
9%
Protein Bcl 2
9%
Exanthem
9%
Aspartate Aminotransferase
9%
Phosphotransferase Inhibitor
9%
Drug Interaction
9%
Agent Study
9%
Program Evaluation
9%
Hypertension
9%
Pharmacology, Toxicology and Pharmaceutical Science
Solid Malignant Neoplasm
100%
Liver Cell Carcinoma
100%
Sorafenib
100%
Navitoclax
100%
Diseases
18%
Malignant Neoplasm
18%
Maximum Tolerated Dose
18%
Neoplasm
9%
Clinical Trial
9%
Thrombocytopenia
9%
Rash
9%
Pharmacokinetic
9%
Phosphotransferase Inhibitor
9%
Drug-Drug Interaction
9%
Pharmacodynamics
9%
Protein Bcl 2
9%
Preclinical Study
9%
Aspartate Aminotransferase
9%
Oral Administration
9%
Hypertension
9%