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NCT00424632 · ClinicalTrials.gov registry record · Phase 1
Phase 1 Study Of Aurora Kinase Inhibitor PF-03814735 In Patients With Advanced Solid Tumors
A Phase 1 study of Solid Tumors, sponsored by Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 57
- Enrollment target
- 2
- Study locations
NCT00424632: Completed Phase 1 study of Solid Tumors, sponsored by Pfizer.
NCT00424632 is a Phase 1 study of Solid Tumors that has completed, run by Pfizer. The registered enrollment target is 57 participants, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (80% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00424632, a Phase 1 study of Solid Tumors, has completed, sponsored by Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 57 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to determine the maximum tolerated dose and recommended phase 2 dose of PF-03814735 administered orally as single agent in patients with advanced solid tumors.
Primary Outcome
DLT defined as any of the following during the first cycle of treatment and attributable to PF-03814735: Grade (Gr) 4 neutropenia (absolute neutrophil count \[ANC\] \<500 cells/mm\^3) for \>7 days or febrile neutropenia (ANC \<1000/mm\^3, fever ≥38 degrees Celsius; neutropenic infection (ANC \<1000/mm\^3); Gr 4 thrombocytopenia (platelets \<25,000 cells/mm\^3); ≥Gr 3 nausea, vomiting, or diarrhea, despite optimal antiemetic, anti-diarrheal support; ≥20% decrease in left ventricular ejection frac
Conditions Studied
Interventions
- DRUG PF-03814735
Study Locations (2)
Tennessee
- Pfizer Investigational Site - Nashville
Other
- Pfizer Investigational Site - Leuven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 57 participants |
| Start Date | 2006-11 |
| Est. Completion | 2009-06 |
| Phase | Phase 1 |
What the finished NCT00424632 record still lists
NCT00424632 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 57 participants, a relatively small participant target, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (80% lower).
The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 1 intervention - of which PF-03814735 is the first listed.
NCT00424632 reports a single indexed study location in Tennessee, Other.
Frequently Asked Questions
What is clinical trial NCT00424632 about?
NCT00424632 is a clinical study titled "Phase 1 Study Of Aurora Kinase Inhibitor PF-03814735 In Patients With Advanced Solid Tumors". The purpose of this study is to determine the maximum tolerated dose and recommended phase 2 dose of PF-03814735 administered orally as single agent in patients with advanced solid tumors.
What is the current status of trial NCT00424632?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 57 participants. The study started on 2006-11. Estimated completion is 2009-06.
What conditions does trial NCT00424632 study?
This clinical trial studies the following conditions: Solid Tumors.
What interventions are being tested in trial NCT00424632?
The interventions under investigation include: PF-03814735 (DRUG).
Who is sponsoring clinical trial NCT00424632?
This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00424632 being conducted?
This trial has 2 study locations across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Solid Tumors
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00424632's enrollment target sits among peer trials
57 77th of 125 higher than 49 of 125 other Solid Tumors trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Solid Tumors trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
A Study of XB371 Administered in Participants With Locally Advanced or Metastatic Solid Tumors
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JAB-2485 Activity in Adult Patients With Advanced Solid Tumors
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A Study to Evaluate INCB161734 in Participants With Advanced or Metastatic Solid Tumors With KRAS G12D Mutation
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-
Study of AUBE00 in Patients With Solid Tumors
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