ASXL1 is altered in 13.44% of acute myeloid leukemia patients with ASXL1 Mutation present in 5.14% of all acute myeloid leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 34 clinical trials for acute myeloid leukemia, of which 28 are open and 6 are closed. Of the trials that contain ASXL1 Mutation and acute myeloid leukemia as inclusion criteria, 1 is early phase 1 (1 open), 9 are phase 1 (7 open), 4 are phase 1/phase 2 (4 open), 17 are phase 2 (15 open), 1 is phase 2/phase 3 (0 open), and 2 are phase 3 (1 open) [5].

ASXL1 is altered in 18.89% of myelodysplastic syndromes patients with ASXL1 Mutation present in 5.91% of all myelodysplastic syndromes patients [4].

ASXL1 Mutation is an inclusion criterion in 25 clinical trials for myelodysplastic syndromes, of which 21 are open and 4 are closed. Of the trials that contain ASXL1 Mutation and myelodysplastic syndromes as inclusion criteria, 1 is early phase 1 (1 open), 5 are phase 1 (4 open), 6 are phase 1/phase 2 (6 open), 12 are phase 2 (10 open), and 1 is phase 2/phase 3 (0 open) [5].

ASXL1 is altered in 39.04% of chronic myelomonocytic leukemia patients with ASXL1 Mutation present in 10.7% of all chronic myelomonocytic leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 11 clinical trials for chronic myelomonocytic leukemia, of which 9 are open and 2 are closed. Of the trials that contain ASXL1 Mutation and chronic myelomonocytic leukemia as inclusion criteria, 3 are phase 1 (2 open), 2 are phase 1/phase 2 (2 open), and 6 are phase 2 (5 open) [5].

ASXL1 Mutation is an inclusion criterion in 9 clinical trials for acute lymphoblastic leukemia, of which 9 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and acute lymphoblastic leukemia as inclusion criteria, 1 is early phase 1 (1 open), 2 are phase 1 (2 open), and 6 are phase 2 (6 open) [5].

ASXL1 is altered in 12.05% of secondary acute myeloid leukemia patients with ASXL1 Mutation present in 6.02% of all secondary acute myeloid leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 5 clinical trials for secondary acute myeloid leukemia, of which 5 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and secondary acute myeloid leukemia as inclusion criteria, 2 are phase 1 (2 open), 1 is phase 1/phase 2 (1 open), and 2 are phase 2 (2 open) [5].

ASXL1 is altered in 2.45% of multiple myeloma patients with ASXL1 Mutation present in 1.22% of all multiple myeloma patients [4].

ASXL1 Mutation is an inclusion criterion in 5 clinical trials for multiple myeloma, of which 4 are open and 1 is closed. Of the trials that contain ASXL1 Mutation and multiple myeloma as inclusion criteria, 1 is early phase 1 (1 open), 1 is phase 1 (1 open), 1 is phase 1/phase 2 (1 open), and 2 are phase 2 (1 open) [5].

ASXL1 is altered in 10.26% of chronic myeloid leukemia patients with ASXL1 Mutation present in 2.56% of all chronic myeloid leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 4 clinical trials for chronic myeloid leukemia, of which 4 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and chronic myeloid leukemia as inclusion criteria, 2 are phase 1 (2 open), 1 is phase 1/phase 2 (1 open), and 1 is phase 2 (1 open) [5].

ASXL1 is altered in 1.79% of hodgkin lymphoma patients with ASXL1 Mutation present in 1.79% of all hodgkin lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 4 clinical trials for hodgkin lymphoma, of which 4 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and hodgkin lymphoma as inclusion criteria, 1 is phase 1 (1 open), 1 is phase 1/phase 2 (1 open), and 2 are phase 2 (2 open) [5].

ASXL1 is altered in 2.08% of non-hodgkin lymphoma patients with ASXL1 Mutation present in 1.3% of all non-hodgkin lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 4 clinical trials for non-hodgkin lymphoma, of which 4 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and non-hodgkin lymphoma as inclusion criteria, 1 is early phase 1 (1 open), 1 is phase 1 (1 open), and 2 are phase 2 (2 open) [5].

ASXL1 Mutation is an inclusion criterion in 4 clinical trials for acute myeloid leukemia arising from previous myelodysplastic syndrome, of which 4 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and acute myeloid leukemia arising from previous myelodysplastic syndrome as inclusion criteria, 1 is phase 1 (1 open) and 3 are phase 2 (3 open) [5].

ASXL1 is altered in 12.05% of therapy-related acute myeloid leukemia patients with ASXL1 Mutation present in 6.02% of all therapy-related acute myeloid leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 3 clinical trials for therapy-related acute myeloid leukemia, of which 3 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and therapy-related acute myeloid leukemia as inclusion criteria, 1 is phase 1 (1 open) and 2 are phase 2 (2 open) [5].

ASXL1 Mutation is an inclusion criterion in 3 clinical trials for T-cell acute lymphoblastic leukemia, of which 3 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and T-cell acute lymphoblastic leukemia as inclusion criteria, 1 is phase 1/phase 2 (1 open) and 2 are phase 2 (2 open) [5].

ASXL1 is altered in 21.69% of myelofibrosis patients with ASXL1 Mutation present in 9.04% of all myelofibrosis patients [4].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for myelofibrosis, of which 1 is open and 1 is closed. Of the trials that contain ASXL1 Mutation and myelofibrosis as inclusion criteria, 2 are phase 2 (1 open) [5].

ASXL1 is altered in 33.92% of myelodysplastic/myeloproliferative neoplasm patients with ASXL1 Mutation present in 8.04% of all myelodysplastic/myeloproliferative neoplasm patients [4].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for myelodysplastic/myeloproliferative neoplasm, of which 2 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and myelodysplastic/myeloproliferative neoplasm as inclusion criteria, 1 is phase 1/phase 2 (1 open) and 1 is phase 2 (1 open) [5].

ASXL1 is altered in 11.27% of secondary myelodysplastic syndrome patients with ASXL1 Mutation present in 4.23% of all secondary myelodysplastic syndrome patients [4].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for secondary myelodysplastic syndrome, of which 1 is open and 1 is closed. Of the trials that contain ASXL1 Mutation and secondary myelodysplastic syndrome as inclusion criteria, 2 are phase 2 (1 open) [5].

ASXL1 is altered in 11.27% of therapy-related myelodysplastic syndrome patients with ASXL1 Mutation present in 4.23% of all therapy-related myelodysplastic syndrome patients [4].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for therapy-related myelodysplastic syndrome, of which 2 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and therapy-related myelodysplastic syndrome as inclusion criteria, 2 are phase 1 (2 open) [5].

ASXL1 is altered in 1.89% of B-cell non-hodgkin lymphoma patients with ASXL1 Mutation present in 1.29% of all B-cell non-hodgkin lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for B-cell non-hodgkin lymphoma, of which 2 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and B-cell non-hodgkin lymphoma as inclusion criteria, 1 is phase 1/phase 2 (1 open) and 1 is phase 2 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for B-cell acute lymphoblastic leukemia, of which 2 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and B-cell acute lymphoblastic leukemia as inclusion criteria, 1 is phase 1/phase 2 (1 open) and 1 is phase 2 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 2 clinical trials for chronic lymphocytic leukemia, of which 2 are open and 0 are closed. Of the trials that contain ASXL1 Mutation and chronic lymphocytic leukemia as inclusion criteria, 1 is phase 1/phase 2 (1 open) and 1 is phase 2 (1 open) [5].

ASXL1 is altered in 24.78% of primary myelofibrosis patients with ASXL1 Mutation present in 10.18% of all primary myelofibrosis patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for primary myelofibrosis, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and primary myelofibrosis as inclusion criteria, 1 is phase 1/phase 2 (1 open) [5].

ASXL1 is altered in 29.73% of chronic myelomonocytic leukemia-1 patients with ASXL1 Mutation present in 8.11% of all chronic myelomonocytic leukemia-1 patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for chronic myelomonocytic leukemia-1, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and chronic myelomonocytic leukemia-1 as inclusion criteria, 1 is phase 1/phase 2 (1 open) [5].

ASXL1 is altered in 21.67% of acute myeloid leukemia with myelodysplasia-related changes patients with ASXL1 Mutation present in 7.33% of all acute myeloid leukemia with myelodysplasia-related changes patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for acute myeloid leukemia with myelodysplasia-related changes, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and acute myeloid leukemia with myelodysplasia-related changes as inclusion criteria, 1 is phase 2/phase 3 (0 open) [5].

ASXL1 is altered in 50.0% of chronic myelomonocytic leukemia-2 patients with ASXL1 Mutation present in 7.14% of all chronic myelomonocytic leukemia-2 patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for chronic myelomonocytic leukemia-2, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and chronic myelomonocytic leukemia-2 as inclusion criteria, 1 is phase 1/phase 2 (1 open) [5].

ASXL1 is altered in 16.17% of myeloproliferative neoplasm patients with ASXL1 Mutation present in 6.09% of all myeloproliferative neoplasm patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for myeloproliferative neoplasm, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and myeloproliferative neoplasm as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 6.18% of melanoma patients with ASXL1 Mutation present in 5.85% of all melanoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for melanoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and melanoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 14.48% of leukemia patients with ASXL1 Mutation present in 5.19% of all leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for leukemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and leukemia as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 13.15% of acute leukemia patients with ASXL1 Mutation present in 5.04% of all acute leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for acute leukemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and acute leukemia as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 19.53% of refractory anemia with excess blasts patients with ASXL1 Mutation present in 4.65% of all refractory anemia with excess blasts patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for refractory anemia with excess blasts, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and refractory anemia with excess blasts as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 48.0% of chronic myelomonocytic leukemia-0 patients with ASXL1 Mutation present in 4.0% of all chronic myelomonocytic leukemia-0 patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for chronic myelomonocytic leukemia-0, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and chronic myelomonocytic leukemia-0 as inclusion criteria, 1 is phase 1/phase 2 (1 open) [5].

ASXL1 is altered in 20.0% of myelodysplastic syndrome with excess blasts-2 patients with ASXL1 Mutation present in 4.0% of all myelodysplastic syndrome with excess blasts-2 patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for myelodysplastic syndrome with excess blasts-2, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and myelodysplastic syndrome with excess blasts-2 as inclusion criteria, 1 is phase 2 (0 open) [5].

ASXL1 is altered in 5.03% of bladder carcinoma patients with ASXL1 Mutation present in 3.65% of all bladder carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for bladder carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and bladder carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 6.86% of polycythemia vera patients with ASXL1 Mutation present in 3.43% of all polycythemia vera patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for polycythemia vera, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and polycythemia vera as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 7.91% of colorectal carcinoma patients with ASXL1 Mutation present in 3.41% of all colorectal carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for colorectal carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and colorectal carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 3.71% of anaplastic astrocytoma patients with ASXL1 Mutation present in 2.92% of all anaplastic astrocytoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for anaplastic astrocytoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and anaplastic astrocytoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 3.27% of glioblastoma patients with ASXL1 Mutation present in 2.89% of all glioblastoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for glioblastoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and glioblastoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 3.32% of non-small cell lung carcinoma patients with ASXL1 Mutation present in 2.81% of all non-small cell lung carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for non-small cell lung carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and non-small cell lung carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 4.63% of head and neck carcinoma patients with ASXL1 Mutation present in 2.63% of all head and neck carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for head and neck carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and head and neck carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 3.73% of malignant solid tumor patients with ASXL1 Mutation present in 2.51% of all malignant solid tumor patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for malignant solid tumor, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and malignant solid tumor as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 4.3% of histiocytic and dendritic cell neoplasm patients with ASXL1 Mutation present in 2.34% of all histiocytic and dendritic cell neoplasm patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for histiocytic and dendritic cell neoplasm, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and histiocytic and dendritic cell neoplasm as inclusion criteria, 1 is phase 1/phase 2 (1 open) [5].

ASXL1 is altered in 4.17% of mixed phenotype acute leukemia patients with ASXL1 Mutation present in 2.08% of all mixed phenotype acute leukemia patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for mixed phenotype acute leukemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and mixed phenotype acute leukemia as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 3.02% of diffuse large B-cell lymphoma patients with ASXL1 Mutation present in 1.89% of all diffuse large B-cell lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for diffuse large B-cell lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and diffuse large B-cell lymphoma as inclusion criteria, 1 is early phase 1 (1 open) [5].

ASXL1 is altered in 3.06% of ovarian carcinoma patients with ASXL1 Mutation present in 1.81% of all ovarian carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for ovarian carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and ovarian carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 2.82% of mature T-cell and NK-cell neoplasm patients with ASXL1 Mutation present in 1.64% of all mature T-cell and NK-cell neoplasm patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for mature T-cell and NK-cell neoplasm, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and mature T-cell and NK-cell neoplasm as inclusion criteria, 1 is phase 1/phase 2 (1 open) [5].

ASXL1 is altered in 2.39% of breast carcinoma patients with ASXL1 Mutation present in 1.6% of all breast carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for breast carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and breast carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 2.91% of T-cell non-hodgkin lymphoma patients with ASXL1 Mutation present in 1.45% of all T-cell non-hodgkin lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for T-cell non-hodgkin lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and T-cell non-hodgkin lymphoma as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 3.3% of indolent non-hodgkin lymphoma patients with ASXL1 Mutation present in 1.42% of all indolent non-hodgkin lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for indolent non-hodgkin lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and indolent non-hodgkin lymphoma as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 is altered in 2.17% of lymphoma patients with ASXL1 Mutation present in 1.3% of all lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for lymphoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and lymphoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 1.67% of sarcoma patients with ASXL1 Mutation present in 1.3% of all sarcoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for sarcoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and sarcoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 is altered in 1.86% of chronic lymphocytic leukemia/small lymphocytic lymphoma patients with ASXL1 Mutation present in 1.18% of all chronic lymphocytic leukemia/small lymphocytic lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for chronic lymphocytic leukemia/small lymphocytic lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and chronic lymphocytic leukemia/small lymphocytic lymphoma as inclusion criteria, 1 is phase 1 (1 open) [5].

ASXL1 is altered in 1.12% of mantle cell lymphoma patients with ASXL1 Mutation present in 1.12% of all mantle cell lymphoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for mantle cell lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and mantle cell lymphoma as inclusion criteria, 1 is early phase 1 (1 open) [5].

ASXL1 is altered in 1.08% of pancreatic carcinoma patients with ASXL1 Mutation present in 0.79% of all pancreatic carcinoma patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for pancreatic carcinoma, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and pancreatic carcinoma as inclusion criteria, 1 is phase 1 (0 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for acute bilineal leukemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and acute bilineal leukemia as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for acute biphenotypic leukemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and acute biphenotypic leukemia as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for aplastic anemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and aplastic anemia as inclusion criteria, 1 is phase 1 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for double-hit lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and double-hit lymphoma as inclusion criteria, 1 is early phase 1 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for lymphoblastic lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and lymphoblastic lymphoma as inclusion criteria, 1 is phase 1 (1 open) [5].

ASXL1 is altered in 30.3% of myelodysplastic/myeloproliferative neoplasm, unclassifiable patients [4].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for myelodysplastic/myeloproliferative neoplasm, unclassifiable, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and myelodysplastic/myeloproliferative neoplasm, unclassifiable as inclusion criteria, 1 is phase 1 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for peripheral T-cell lymphoma, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and peripheral T-cell lymphoma as inclusion criteria, 1 is early phase 1 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for plasma cell leukemia, of which 0 are open and 1 is closed. Of the trial that contains ASXL1 Mutation and plasma cell leukemia as inclusion criteria, 1 is phase 2 (0 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for refractory anemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and refractory anemia as inclusion criteria, 1 is phase 2 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for therapy-related chronic myelomonocytic leukemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and therapy-related chronic myelomonocytic leukemia as inclusion criteria, 1 is phase 1 (1 open) [5].

ASXL1 Mutation is an inclusion criterion in 1 clinical trial for waldenstrom macroglobulinemia, of which 1 is open and 0 are closed. Of the trial that contains ASXL1 Mutation and waldenstrom macroglobulinemia as inclusion criteria, 1 is phase 2 (1 open) [5].