Despite recent breakthroughs with immuno-oncology agents in cancer treatment, patients with certain types of solid tumors still have few or no options and are in need of treatments to extend life. These patients have significant unmet medical needs.
Birinapant is being developed to enhance responses, and extend survival, of patients with solid tumors where existing treatments do not provide sufficient survival benefit, or where patients no longer have treatment options. Based on its unique design and mechanism, birinapant has the potential to enhance patients’ responses in combination with other treatments.
IGM Biosciences Inc.
In January 2021 Medivir entered into a licensing agreement with IGM Biosciences Inc. (IGM) regarding the global, exclusive development rights for birinapant. IGM plans to initially study birinapant in kombination with its antibody IGM-8444 against Death Receptor 5, which is in the clinical development phase.
Birinapant is a SMAC mimetic that in an efficient way binds to and degrades Inhibitors of Apoptosis Proteins (IAPs), causing their degradation which enables cell death (apoptosis) in tumor cells. At the same time, the immune system’s response is augmented, enhancing its attack on the tumor. Through its double action, on both tumor cells and cells of the immune system, birinapant has the potential to improve the treatment of several types of cancer when used in combination with other drugs.
In October 2019, the first patient was enrolled in a phase I study to investigate the safety and tolerability of a combination treatment of birinapant and radiation therapy in patients with recurrent Head and Neck Squamous Cell Carcinoma.
The study is sponsored and financed as part of the US National Cancer Institute (NCI)’s Cancer Therapy Evaluation Program (CTEP). Medivir provides birinapant and will be afforded full access to all reports from the study
The primary goals are to evaluate the safety of the combination treatment and to establish a maximum tolerated dose for further studies
Medivir’s decision to support this study was based on preclinical data from NCI showing good effects from birinapant in combination with radiotherapy in models of various types of cancer of the head and neck region1).
1) DF Eytan et al., SMAC Mimetic Birinapant plus Radiation Eradicates Human Head and Neck Cancers with Genomic Amplifications of Cell Death Genes FADD and BIRC2. Cancer Research (2016) 76, 5442-5454.
In August 2017, Medivir initiated a clinical phase I/II study of birinapant in combination with MSD’s anti-PD-1 therapy Keytruda® (pembroluzimab) to investigate birinapant’s effect as a combination treatment for patients with treatment-resistant solid tumors.
The phase I study showed a positive safety profile and identified the recommended phase II dose of birinapant in combination with Keytruda®.
In an interim analysis of patients treated with birinapant up to and including the dose of 17 mg/m2, one of the patients with MSS colorectal cancer showed a confirmed partial response and the treatment continued for two years. Three patients achieved stable disease lasting up to 18 weeks.
The phase II part of the study was initiated in December 2018 to evaluate preliminary efficacy, as well as safety and tolerability, for birinapant in combination with Keytruda® in a patient group with MSS colorectal cancer. On the basis of a futility analysis of data from 14 treated patients the study was discontinued in December 2019.