Urelumab
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This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.
Identification
- Generic Name
- Urelumab
- DrugBank Accession Number
- DB12077
- Background
Urelumab has been used in trials studying the treatment of Leukemia, Multiple Myeloma, Malignant Tumors, and Cancer - Solid Tumors and B-Cell Non-Hodgkin's Lymphoma. Urelumab is a fully human antibody that targets CD137. The antibody product was developed using Medarex's UltiMAb(R) technology and was the first UltiMAb- derived antibody in clinical development by Bristol-Myers Squibb under the December 2003 agreement with Medarex.
- Type
- Biotech
- Groups
- Investigational
- Biologic Classification
- Protein Based Therapies
Monoclonal antibody (mAb) - Protein Chemical Formula
- Not Available
- Protein Average Weight
- Not Available
- Sequences
- Not Available
- Synonyms
- Urelumab
- External IDs
- BMS 663513
- BMS-663513
- BMS-66513
Pharmacology
- Indication
Not Available
Reduce drug development failure ratesBuild, train, & validate machine-learning modelswith evidence-based and structured datasets.Build, train, & validate predictive machine-learning models with structured datasets.- Contraindications & Blackbox Warnings
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- Pharmacodynamics
Not Available
- Mechanism of action
Target Actions Organism UTumor necrosis factor receptor superfamily member 9 Not Available Humans - Absorption
Not Available
- Volume of distribution
Not Available
- Protein binding
Not Available
- Metabolism
- Not Available
- Route of elimination
Not Available
- Half-life
Not Available
- Clearance
Not Available
- Adverse Effects
- Improve decision support & research outcomesWith structured adverse effects data, including: blackbox warnings, adverse reactions, warning & precautions, & incidence rates.Improve decision support & research outcomes with our structured adverse effects data.
- Toxicity
Not Available
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs
- Not Available
Interactions
- Drug Interactions
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your softwareAbciximab The risk or severity of adverse effects can be increased when Abciximab is combined with Urelumab. Adalimumab The risk or severity of adverse effects can be increased when Adalimumab is combined with Urelumab. Aducanumab The risk or severity of adverse effects can be increased when Urelumab is combined with Aducanumab. Alemtuzumab The risk or severity of adverse effects can be increased when Alemtuzumab is combined with Urelumab. Alirocumab The risk or severity of adverse effects can be increased when Alirocumab is combined with Urelumab. Amivantamab The risk or severity of adverse effects can be increased when Urelumab is combined with Amivantamab. Anifrolumab The risk or severity of adverse effects can be increased when Anifrolumab is combined with Urelumab. Ansuvimab The risk or severity of adverse effects can be increased when Urelumab is combined with Ansuvimab. Anthrax immune globulin human The risk or severity of adverse effects can be increased when Anthrax immune globulin human is combined with Urelumab. Antilymphocyte immunoglobulin (horse) The risk or severity of adverse effects can be increased when Antilymphocyte immunoglobulin (horse) is combined with Urelumab. Identify potential medication risksEasily compare up to 40 drugs with our drug interaction checker.Get severity rating, description, and management advice.Learn more - Food Interactions
- Not Available
Categories
- Drug Categories
- Chemical TaxonomyProvided by Classyfire
- Description
- Not Available
- Kingdom
- Organic Compounds
- Super Class
- Organic Acids
- Class
- Carboxylic Acids and Derivatives
- Sub Class
- Amino Acids, Peptides, and Analogues
- Direct Parent
- Peptides
- Alternative Parents
- Not Available
- Substituents
- Not Available
- Molecular Framework
- Not Available
- External Descriptors
- Not Available
- Affected organisms
- Not Available
Chemical Identifiers
- UNII
- 230902QLLC
- CAS number
- 934823-49-1
References
Clinical Trials
- Clinical Trials
Phase Status Purpose Conditions Count 2 Active Not Recruiting Treatment Bladder Cancer / Urothelial Carcinoma 1 2 Completed Treatment Melanoma 1 2 Recruiting Treatment Pancreatic Cancer 1 2 Withdrawn Treatment Leukemias 1 1 Active Not Recruiting Treatment High Grade Glioma: Glioblastoma (GBM) / High Grade Glioma: Gliosarcoma / Recurrent Brain Neoplasm 1 1 Completed Treatment B-cell Malignancy 1 1 Completed Treatment Cancer 1 1 Completed Treatment Cancer - Solid Tumors and B-Cell Non-Hodgkin's Lymphoma 1 1 Completed Treatment Colorectal Cancer / Head And Neck Cancer 1 1 Completed Treatment Malignant Neoplasm 1
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
- Not Available
- Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Not Available
- Experimental Properties
- Not Available
Targets

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- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- Unknown
- General Function
- Tumor necrosis factor-activated receptor activity
- Specific Function
- Receptor for TNFSF9/4-1BBL. Possibly active during T cell activation.
- Gene Name
- TNFRSF9
- Uniprot ID
- Q07011
- Uniprot Name
- Tumor necrosis factor receptor superfamily member 9
- Molecular Weight
- 27898.6 Da
Drug created at October 20, 2016 21:18 / Updated at February 21, 2021 18:53