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Clinical Trial Summary

The purpose of this open-label, multi center, phase I study, was to determine the safety profile of PHA-793887 administered by intravenous infusion to patients with advanced/metastatic solid tumors. This was a dose-finding study to determine the maximum tolerated dose and the dose of PHA-793887 that can be safely used in phase II investigations.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00996255
Study type Interventional
Source Nerviano Medical Sciences
Contact
Status Terminated
Phase Phase 1
Start date November 2006
Completion date February 2008

See also
  Status Clinical Trial Phase
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Active, not recruiting NCT04182516 - Study of NMS-03305293 in Pts With Selected Advanced/Metastatic Solid Tumors Phase 1
Terminated NCT02444793 - A Study of PF-05082566 In Combination With Mogamulizumab In Patients With Advanced Solid Tumors Phase 1
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Recruiting NCT05405595 - ADG126 in Combination With Pembrolizumab in Patients With Advanced/Metastatic Solid Tumors Phase 1/Phase 2
Completed NCT02665416 - Study Evaluating the Safety, Pharmacokinetics (PK), Pharmacodynamics (PD), and Therapeutic Activity of Selicrelumab (RO7009789) With Vanucizumab or Bevacizumab in Participants With Metastatic Solid Tumors Phase 1
Terminated NCT01092052 - Study of NMS-1116354 in Advanced/Metastatic Solid Tumors Phase 1
Completed NCT05277402 - ADG116 in Combination With Pembrolizumab in Patients With Advanced/Metastatic Solid Tumors Phase 1
Recruiting NCT05614258 - Study of ADG206 in Subjects With Advanced/Metastatic Solid Tumors Phase 1
Active, not recruiting NCT05394168 - A Phase I Clinical Study of HLX53 in Advanced/Metastatic Solid Tumors Phase 1