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WithdrawnNCT00040989Updated Jul 10, 2013

BAY 56-3722 in Treating Patients With Recurrent, Unresectable, or Metastatic Kidney Cancer

A Phase 2 interventional study of BAY 56-3722 and enzyme inhibitor therapy in Stage IV Renal Cell Cancer and Recurrent Renal Cell Cancer, sponsored by Jonsson Comprehensive Cancer Center. Withdrawn at 26 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-07-10.

Sponsored by Jonsson Comprehensive Cancer Center · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
0
Ages
18 Years and older
Sex
All
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Study summary

RATIONALE: BAY 56-3722 may stop the growth of cancer cells by blocking the enzymes necessary for tumor cell growth.

PURPOSE: Phase II trial to study the effectiveness of BAY 56-3722 in treating patients who have recurrent, unresectable, or metastatic kidney cancer.

Read the detailed description

OBJECTIVES:

  • Determine the tumor response rate of patients with recurrent, unresectable, or metastatic renal cell carcinoma treated with BAY 56-3722.
  • Determine the duration of response, time to progression, and survival of patients treated with this drug.
  • Determine the qualitative and quantitative toxic effects of this drug in these patients.
  • Determine the pharmacokinetics of this drug in these patients.

OUTLINE: This is a multicenter study.

Patients receive BAY 56-3722 IV over 30 minutes on days 1-3. Treatment repeats every 3 weeks for at least 2 courses in the absence of disease progression or unacceptable toxicity.

Patients are followed every 6 months.

PROJECTED ACCRUAL: A total of 20-140 patients will be accrued for this study.

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Conditions studied

  • Stage IV Renal Cell Cancer
  • Recurrent Renal Cell Cancer
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In context

Carcinoma, Renal Cell

1,965 studies on the registry are indexed under Carcinoma, Renal Cell; 377 are open to participants now.

Browse Carcinoma, Renal Cell studies →

Lead sponsor

Jonsson Comprehensive Cancer Center is the lead sponsor of 396 studies on the registry; 67 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 2 (5%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed renal cell carcinoma (RCC)
  • Recurrent AND unresectable disease OR
  • Unresectable disease OR
  • Metastatic disease
  • At least 1 bidimensionally measurable lesion by CT scan or MRI
  • No metastatic brain or meningeal tumors unless more than 3 months since prior surgery and/or gamma knife radiosurgery, 2 subsequent negative imaging studies at least 4 weeks apart, clinically stable, and no concurrent corticosteroids or anticonvulsants

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • ECOG 0-2

Life expectancy:

  • At least 12 weeks

Hematopoietic:

  • Absolute neutrophil count at least 1,500/mm\^3
  • Platelet count at least 100,000/mm\^3
  • Hemoglobin at least 9 g/dL

Hepatic:

  • Bilirubin no greater than 1.5 times upper limit of normal (ULN)
  • AST and ALT less than 2.5 times ULN (5 times ULN if liver metastases present)
  • No chronic hepatitis B or C

Renal:

  • Creatinine no greater than 1.5 mg/dL
  • Calcium normal

Cardiovascular:

  • No clinically evident congestive heart failure
  • No serious cardiac arrhythmias
  • No symptoms of coronary heart disease
  • No symptoms of ischemia

Other:

  • HIV negative
  • No active infections requiring systemic antibacterial, antifungal, or antiviral therapy
  • No other malignancy within the past 3 years except carcinoma in situ of the cervix, adequately treated basal cell carcinoma, or superficial bladder tumors (Ta, Tis, or T1)
  • No substance abuse
  • No medical, psychological, or social conditions that would preclude study
  • No known or suspected allergy to study drug or any other study agents
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for at least 6 months after study

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • No prior anticancer vaccine therapy
  • No prior bone marrow transplantation or stem cell rescue
  • More than 4 weeks since prior thalidomide and bevacizumab
  • At least 4 weeks since prior interleukin-2 and interferon
  • No more than 2 prior regimens
  • No concurrent bone marrow transplantation or stem cell rescue

Chemotherapy:

  • No prior cytotoxic chemotherapy
  • No concurrent cytotoxic chemotherapy

Endocrine therapy:

  • See Disease Characteristics
  • No prior hormonal therapy for RCC
  • No concurrent hormonal therapy for RCC

Radiotherapy:

  • See Disease Characteristics
  • More than 4 weeks since prior radiotherapy
  • No prior radiotherapy to indicator lesion unless progression is documented

Surgery:

  • See Disease Characteristics
  • More than 3 weeks since prior major surgery

Other:

  • At least 4 weeks since prior investigational anticancer drugs
  • No other concurrent investigational anticancer drugs
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Study design

Phase
Phase 2
Primary purpose
Treatment
Enrollment
0 participants (actual)

Interventions

  • DrugBAY 56-3722
  • Procedureenzyme inhibitor therapy
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Study locations

26 sites
  • University of Arkansas for Medical Sciences
    Little Rock, Arkansas 72205, United States
  • USC/Norris Comprehensive Cancer Center and Hospital
    Los Angeles, California 90033-0804, United States
  • Jonsson Comprehensive Cancer Center, UCLA
    Los Angeles, California 90095-1781, United States
  • University of Colorado Cancer Center
    Denver, Colorado 80010, United States
  • Oncology-Hematology Group of South Florida
    Miami, Florida 33176, United States
  • Emory University Hospital - Atlanta
    Atlanta, Georgia 30322, United States
  • Veterans Affairs Medical Center - Atlanta (Decatur)
    Decatur, Georgia 30033, United States
  • Dwight David Eisenhower Army Medical Center
    Fort Gordon, Georgia 30905-5650, United States
  • Loyola University Medical Center
    Maywood, Illinois 60153, United States
  • University of Kansas Medical Center
    Kansas City, Kansas 66160-7353, United States
  • Tulane University School of Medicine
    New Orleans, Louisiana 70112, United States
  • Louisiana State University Health Sciences Center - Shreveport
    Shreveport, Louisiana 71130-3932, United States
  • Dana-Farber Cancer Institute
    Boston, Massachusetts 02115, United States
  • Ellis Fischel Cancer Center - Columbia
    Columbia, Missouri 65203, United States
  • University of Nebraska Medical Center
    Omaha, Nebraska 68198-3330, United States
  • Norris Cotton Cancer Center
    Lebanon, New Hampshire 03756-0002, United States
  • Hackensack University Medical Center
    Hackensack, New Jersey 07601, United States
  • Cancer Institute of New Jersey
    New Brunswick, New Jersey 08903, United States
  • University of Rochester Medical Center
    Rochester, New York 14642-0001, United States
  • Cleveland Clinic Taussig Cancer Center
    Cleveland, Ohio 44195, United States
  • Oregon Cancer Institute
    Portland, Oregon 97239, United States
  • University of Pennsylvania Cancer Center
    Philadelphia, Pennsylvania 19104-4283, United States
  • Cancer Centers of the Carolinas
    Greenville, South Carolina 29615, United States
  • Simmons Cancer Center - Dallas
    Dallas, Texas 75390, United States
  • Baylor College of Medicine
    Houston, Texas 77030, United States
  • Cancer Therapy and Research Center
    San Antonio, Texas 78229-3264, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 10, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00040989
Lead sponsor
Jonsson Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)
First posted
Jan 27, 2003
Last update
Jul 10, 2013

Study contacts

Barbara J. Gitlitz, MD
study chair · Jonsson Comprehensive Cancer Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Dec 2006. You cannot join it, but the record below documents what was studied.

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