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MORAb-003 is intravenously administered to Japanese patients with folate receptor-alpha expressing solid tumor once a week for 4 weeks as 1 cycle in order to investigate dose-limiting toxicity and estimate maximum tolerated dose.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MORAb-003 | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MORAb-003 | Drug | MORAb-003 is intravenously administered to patients with solid tumor once a week for 4 weeks as 1 cycle in order to investigate dose-limiting toxicity and estimate maximum tolerated dose |
| Measure | Description | Time Frame |
|---|---|---|
| To investigate dose-limiting toxicity and estimate maximum tolerated dose. | 7 weeks |
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Inclusion criteria;
Exclusion criteria
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| Name | Affiliation | Role |
|---|---|---|
| Chifumi Kitamura | JAC PCU Eisai Co., Ltd. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hidaka-shi | Saitama | Japan | ||||
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25380636 | Derived | Sasaki Y, Miwa K, Yamashita K, Sunakawa Y, Shimada K, Ishida H, Hasegawa K, Fujiwara K, Kodaira M, Fujiwara Y, Namiki M, Matsuda M, Takeuchi Y, Katsumata N. A phase I study of farletuzumab, a humanized anti-folate receptor alpha monoclonal antibody, in patients with solid tumors. Invest New Drugs. 2015 Apr;33(2):332-40. doi: 10.1007/s10637-014-0180-8. Epub 2014 Nov 9. |
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| C527484 | farletuzumab |
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| Chuo-ku |
| Tokyo |
| Japan |