CC-90002 |
NCT02641002 |
Celgene Corp |
CC-90002 |
Subjects With AML and High-Risk MDS |
28 |
Adults (18 and over) |
Phase I |
Terminted |
2016/3/1 |
Interventional; Treatment; Open Label; Single Group Assignment |
Safety; Efficacy; Pharmacokinetics |
terminated (preliminary monotherapy data did not offer a sufficiently encouraging profile for further dose escalation/expansion) |
[61] |
TJ011133 |
NCT04202003 |
I-Mab Biopharma Co Ltd |
TJ011133 |
r/r AML/MDS |
5 |
Adults (18–79 years) |
Phase I |
Recruiting |
2020/3/25 |
Interventional; Treatment; Non-Randomized; Open Label; Single Group Assignment |
Efficacy |
20% achieved morphologic leukemia-free state |
[62] |
Hu5F9-G4 |
NCT03248479 |
Gilead Sciences Inc |
Hu5F9-G4; AZA |
untreated AML/MDS |
68 |
Adults (18 and over) |
Phase I |
Recruiting |
2017/9/8 |
Interventional; Treatment; Non-Randomized; Open Label; Parallel Assignment |
Safety; Efficacy; Pharmacokinetics |
ORR: 79%; CR/CRi: 56% |
[63] |
Hu5F9-G4 |
NCT04435691 |
MD Anderson Cancer Center |
Hu5F9-G4; AZA; VEN |
Patients (pts) with Newly Diagnosed AML |
23 |
Adults (18 and over) |
Phase I/II |
Recruiting |
2020/7/28 |
Interventional; Treatment; Open Label; Single Group Assignment |
Safety; Efficacy |
CR/CRi: 100% |
[64] |
Hu5F9-G4 |
NCT04435691 |
MD Anderson Cancer Center |
Hu5F9-G4; AZA; VEN |
Patients (pts) with R/R-post-VEN failure AML |
13 |
Adults (18 and over) |
Phase I/II |
Recruiting |
2020/7/28 |
Interventional; Treatment; Open Label; Single Group Assignment |
Safety; Efficacy |
CR/CRi: 27% |
[64] |
Hu5F9-G4 |
NCT04435691 |
MD Anderson Cancer Center |
Hu5F9-G4; AZA; VEN |
Patients (pts) with R/R-VEN naive AML |
8 |
Adults (18 and over) |
Phase I/II |
Recruiting |
2020/7/28 |
Interventional; Treatment; Open Label; Single Group Assignment |
Safety; Efficacy |
CR/CRi: 63% |
[64] |