Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00706355 · ClinicalTrials.gov registry record · Phase 1

A Study of PF-04217903 in Patients With Advanced Cancer

A Phase 1 study, sponsored by Pfizer.

Terminated
Registry status
Phase 1
Development phase
16
Enrollment target

NCT00706355: Clinical Trial Phase 1 study, sponsored by Pfizer.

NCT00706355 is a Phase 1 study that was terminated before completion, run by Pfizer. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00706355, a Phase 1 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

PF-04217903 may work in cancer by blocking the cell growth, migration and invasion of tumor cells. PF-04217903 is a new member in a class of drugs called c-Met/hepatocyte growth factor receptor tyrosine kinase inhibitors. This research study is the first time PF-04217903 will be given to patients. PF-04217903 is taken by mouth daily.

Primary Outcome

MTD: dose level at which 1 of 6 participants experienced dose-limiting toxicity (DLT) after 21 days of treatment (Cycle 1). DLT: grade (Gr) 2 elevated creatinine, acute renal failure, Gr 3 thrombocytopenia with bleeding, hypertension (if unmanageable),Gr \>=3 non-hematological non-disease-related (NDR) toxicities (except alopecia,Gr 3/4 hypophosphatemia, hyperuricemia), Gr 3/4 nausea, vomiting, diarrhea, Gr 4 neutropenia, thrombocytopenia lasting for \>=7 days, febrile neutropenia, neutropenic i

Interventions

  • DRUG PF-04217903

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2008-08
Est. Completion 2011-06
Phase Phase 1
Pfizer

1,845 total trials

Why NCT00706355 stopped before completion

NCT00706355 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 1 intervention - of which PF-04217903 is the first listed.

NCT00706355 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00706355 about?

NCT00706355 is a clinical study titled "A Study of PF-04217903 in Patients With Advanced Cancer". PF-04217903 may work in cancer by blocking the cell growth, migration and invasion of tumor cells. PF-04217903 is a new member in a class of drugs called c-Met/hepatocyte growth factor receptor tyrosine kinase inhibitors. This research study is the first time PF-04217903 will be given to patients. P...

What is the current status of trial NCT00706355?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2008-08. Estimated completion is 2011-06.

What interventions are being tested in trial NCT00706355?

The interventions under investigation include: PF-04217903 (DRUG).

Who is sponsoring clinical trial NCT00706355?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00706355's enrollment target sits among peer trials

16 1786th of 2000 higher than 203 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02422641 · 16 participants · Phase 2

    Prospective Evaluation Of High-Dose Systemic Methotrexate In Patients With Breast Cancer And Leptomeningeal Metastasis

  • NCT02851758 · 16 participants · NA

    Transplantation of Autologously Derived Mitochondria Following Ischemia

  • NCT03291028 · 16 participants

    Analysis of Primary and Metastatic Tumors in Patients With Renal Cell Carcinoma and Urothelial Carcinoma

  • NCT03425526 · 16 participants · Phase 1

    Donor T Cell Therapy in Treating Immunocompromised Patients With Adenovirus-Related Disease

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00706355, the US trial registry maintained by the National Library of Medicine. NCT00706355 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.