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Authors | K J Harrington J Brody M Ingham J Strauss S Cemerski M Wang A Tse A Khilnani A Marabelle T Golan | ||||||||||||
Title | Preliminary results of the first-in-human (FIH) study of MK-1454, an agonist of stimulator of interferon genes (STING), as monotherapy or in combination with pembrolizumab (pembro) in patients with advanced solid tumors or lymphomas | ||||||||||||
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URL | https://academic.oup.com/annonc/article/29/suppl_8/mdy424.015/5141570 | ||||||||||||
Abstract Text | Ann Oncol, Oct 2018, 29 (suppl 8), abstract LBA15 |
Molecular Profile | Treatment Approach |
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Gene Name | Source | Synonyms | Protein Domains | Gene Description | Gene Role |
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Therapy Name | Drugs | Efficacy Evidence | Clinical Trials |
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Ulevostinag | Ulevostinag | 0 | 1 |
Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
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Ulevostinag | MK 1454|MK-1454 | STING1 Agonist 19 | Ulevostinag (MK-1454) is an agonist of the stimulator of interferon genes protein (TMEM173, STING1), that when activated leads to the release of cytokines that stimulate cytotoxic T lymphocytes to enhance the anti-tumor immune response (Ann Oncol, Oct 2018, 29 (suppl 8), abstract LBA15, PMID: 31355488). |
Gene | Variant | Impact | Protein Effect | Variant Description | Associated with drug Resistance |
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Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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