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Study To Evaluate The Safety, Pharmacokinetics, And Pharmacodynamics Of PF-00299804 In Patients With Advanced Solid Tumors

Phase 1
Completed
Conditions
Neoplasms
Interventions
Drug: PF-00299804
Registration Number
NCT00225121
Lead Sponsor
Pfizer
Brief Summary

The primary purpose of this study is to study the side effects of PF-00299804 and determine the highest dose that can be safely administered in patients with advanced cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
121
Inclusion Criteria
  • Malignant solid tumor for which there is no currently approved treatment
  • Adequate bone marrow, liver, cardiac, and kidney function
Read More
Exclusion Criteria
  • Cardiac disease
  • Anticancer therapy within 4-6 weeks (depending on therapy)
  • Pregnant or breast-feeding
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
1PF-00299804open label single arm trial
Primary Outcome Measures
NameTimeMethod
Safety6 months
Secondary Outcome Measures
NameTimeMethod
Pharmacodynamics6 months
Efficacy6 months
Pharmacokinetics6 months

Trial Locations

Locations (9)

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

Dana Farber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

Ronald Reagan UCLA Medical Center

🇺🇸

Los Angeles, California, United States

UCLA Hematology/Oncology

🇺🇸

Los Angeles, California, United States

University of Colorado Hospital

🇺🇸

Aurora, Colorado, United States

Vereniging het Nederlandse Kanker Instituut

🇳🇱

Amsterdam, Netherlands

UCLA Oncology Center

🇺🇸

Los Angeles, California, United States

UCLA Santa Monica Hematology/Oncology

🇺🇸

Santa Monica, California, United States

UCLA Hematology Oncology - Santa Monica

🇺🇸

Santa Monica, California, United States

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