A Dose Finding Study Of A New Medication, PF-00337210 That Will Possibly Decrease Blood Supply To Tumors

NCT01105533 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2013-03-19

Study results available
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Summary

This study will test a new cancer medication to determine if this medication will block blood supply to a tumor and decrease growth of a tumor. This study will also define the safety profile and define the safest dose of this new medication for people who have cancer.

Conditions

Interventions

DRUG

PF-00337210

0.67mg Capsule Once Daily (Accelerated Dose Escalation) Continuous

DRUG

PF-00337210

1mg Capsule Once Daily (Dose Escalation) Continuous

DRUG

PF-00337210

2mg Capsule Once Daily (Dose Escalation) Continuous

DRUG

PF-00337210

4mg Capsule Once Daily (Dose Escalation) Continuous

DRUG

PF-00337210

6mg Capsule Once Daily (Dose Escalation) Continuous

DRUG

PF-00337210

9mg Capsule Once Daily (Dose Escalation) Continuous

DRUG

PF-00337210

8mg Capsule Once Daily (Dose Escalation) Continuous

DRUG

PF-00337210

4mg Capsule Twice Daily (Dose Escalation) Continuous

DRUG

PF-00337210

6mg Capsule Twice Daily (Dose Escalation) Continuous

DRUG

PF-00337210

6mg Capsule Twice Daily (Dose Expansion) Continuous

Sponsors & Collaborators

  • University of Wisconsin, Madison

    collaborator OTHER
  • Pfizer

    lead INDUSTRY

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-05-31
Primary Completion
2010-10-31
Completion
2011-09-30

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01105533 on ClinicalTrials.gov