Clinical trial
An Open Label Phase I Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Maximum Tolerated Dose of BAY79-4620 Administered as an Intravenous Infusion Once Every 2 Weeks in Patients With Advanced Solid Tumors
NCT01065623 is registered in ClinicalTrials.gov with Bayer as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- An Open Label Phase I Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Maximum Tolerated Dose of BAY79-4620 Administered as an Intravenous Infusion Once Every 2 Weeks in Patients With Advanced Solid Tumors
- Lead sponsor
- Bayer
- Phase
- Phase 1
- Overall status
- Terminated
- Start date
- April 30, 2010
- Completion date
- August 31, 2010
- Enrollment
- 2 (actual)
- Sites
- 2
Conditions
As the registry lists them; a condition with its own page is linked.