Drug intelligence / Profile preview

ipilimumab + budesonide

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral, Inhalation, Rectal
01

Overview

Ipilimumab + budesonide is a combination of two drugs used in the context of cancer immunotherapy, particularly for patients with advanced or unresectable melanoma. Ipilimumab is a human monoclonal antibody that targets cytotoxic T-lymphocyte antigen 4 (CTLA-4), thereby blocking an inhibitory signal to T-cells and enhancing immune-mediated antitumor responses[1][6]. Budesonide is a synthetic glucocorticoid with potent anti-inflammatory properties, primarily acting through activation of the glucocorticoid receptor to modulate gene expression and suppress inflammatory pathways[4]. In clinical studies, budesonide has been investigated as prophylaxis for immune-related diarrhea/colitis induced by ipilimumab; however, evidence shows that prophylactic use of budesonide does not reduce the incidence or severity of diarrhea associated with ipilimumab therapy[2][5][8]. Ipilimumab was developed by Bristol Myers Squibb and is approved for metastatic melanoma. Budesonide is widely used for inflammatory conditions such as asthma and Crohn's disease.

02

Targets

GR (Glucocorticoid receptor)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)

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