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Therapy Name | MAK683 |
Synonyms | |
Therapy Description |
MAK683 blocks the interaction between EED and EZH2, potentially resulting in a loss of PRC2 activity, reduced H3K27 trimethylation, and decreased proliferation of tumor cells (J Clin Oncol 40, no. 16_suppl (June 01, 2022) 3083, PMID: 36858198). |
Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
---|---|---|---|---|
MAK683 | MAK 683|EED PPI inhibitor MAK683 | MAK683 blocks the interaction between EED and EZH2, potentially resulting in a loss of PRC2 activity, reduced H3K27 trimethylation, and decreased proliferation of tumor cells (J Clin Oncol 40, no. 16_suppl (June 01, 2022) 3083, PMID: 36858198). |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
ARID1A inact mut | urinary bladder cancer | sensitive | MAK683 | Preclinical - Cell culture | Actionable | In a preclinical study, MAK683 inhibited viability of bladder cancer cell lines harboring ARID1A inactivating mutations in culture (PMID: 35852858). | 35852858 |
ARID1A dec exp | urinary bladder cancer | sensitive | MAK683 | Preclinical - Cell culture | Actionable | In a preclinical study, MAK683 inhibited viability of bladder cancer cell lines with ARID1A knockdown in culture (PMID: 35852858). | 35852858 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|---|---|---|---|---|---|
NCT02900651 | Phase Ib/II | MAK683 | Safety and Efficacy of MAK683 in Adult Patients With Advanced Malignancies | Terminated | USA | ITA | FRA | ESP | DEU | CAN | 4 |