Drug intelligence / Profile preview

ipilimumab + interferon alfa-2b + aldesleukin

Development stage
Discontinued
Lead developer
University of Texas MD Anderson Cancer Center
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Intravenous, Subcutaneous
01

Overview

A combination immunotherapy regimen, also known as IPI-Biotherapy, developed and investigated by the M.D. Anderson Cancer Center for the treatment of metastatic melanoma. The regimen consists of the monoclonal antibody ipilimumab (a CTLA-4 checkpoint inhibitor), the type I interferon cytokine interferon alfa-2b, and the recombinant interleukin-2 cytokine aldesleukin. This triple combination was designed to synergistically enhance the anti-tumor immune response by removing inhibitory signals on T-cells (via ipilimumab) and providing direct stimulatory signals to promote the activation and expansion of cytotoxic T-lymphocytes and natural killer cells (via interferon and aldesleukin). It was primarily evaluated in a Phase I/II clinical trial (NCT00494338) for patients who had previously failed cytotoxic chemotherapy, although the study was ultimately terminated due to slow patient accrual.

Brand names
Yervoy + Intron-A + Proleukin
Other names
Ipilimumab + Interferon + IL-2Ipilimumab + Interferon alfa-2b + Aldesleukin
02

Targets

CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)IFNAR1 (Interferon alpha/beta receptor 1)IL-2R (Interleukin-2/interleukin-15 receptor complex)

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