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CLBQ707A1101 assesses the tolerability, safety, efficacy and pharmacokinetics of gimatecan in Japanese patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Gimatecan | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Gimatecan | Drug |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety and tolerability assessed by Adverse Events | 2.8 years | |
| Anti-tumor activity assessed by RECIST criteria | 2.8 years |
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Inclusion criteria:
Exclusion criteria:
Other protocol-defined inclusion/exclusion criteria may apply
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| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novartis Investigative Site | Chiba | Japan |
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| Label | URL |
|---|---|
| Results for CLBQ707A1101E1 can be found on the Novartis Clinical Trial Results Website | View source |
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| ID | Term |
|---|---|
| C433984 | ST 1481 |
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