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Protocol to Allow Continued Access of Ficlatuzumab to P05538 Patient
This treatment protocol will serve as a mechanism to continue to provide ficlatuzumab to patient 0001-000412, who was previously enrolled under protocol P05538 and whom the investigator believes is deriving clinical benefit from ficlatuzumab treatment.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ficlatuzumab | Drug | humanized anti-hepatocyte growth factor (HGF) monoclonal antibody IV administration at 16.5mg/kg every 2 weeks with a ±2 day window around dosing dates, as long as subject is deriving clinical benefit as determined by the Investigator |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| START | San Antonio | Texas | 78229 | United States |
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| Label | URL |
|---|---|
| Continued Access of Ficlatuzumab to P05538 Patient | View source |
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| ID | Term |
|---|---|
| C583360 | ficlatuzumab |
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