Stage IV Renal Cell CancerPhase 2NCT00040989
BAY 56-3722 in Treating Patients With Recurrent, Unresectable, or Metastatic Kidney Cancer
A Phase 2 study testing BAY 56-3722 and enzyme inhibitor therapy in people with Stage IV Renal Cell Cancer and Recurrent Renal Cell Cancer, run by Jonsson Comprehensive Cancer Center at 26 sites in United States.
Trial 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 more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Stage IV Renal Cell Cancer, Recurrent Renal Cell Cancer
- What is being tested?
- BAY 56-3722 and enzyme inhibitor therapy
- Type of treatment
- Surgery or procedure
- How many people
- 0 participants
- Where
- 26 sitesUnited States
- Study dates
- Start not givento not given
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
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
Trial locations and contacts
26 sites in 1 country.
26 sites in 1 country
United States26 sites
Emory University Hospital - Atlanta
Atlanta, Georgia, 30322
Dana-Farber Cancer Institute
Boston, Massachusetts, 02115
Cleveland Clinic Taussig Cancer Center
Cleveland, Ohio, 44195
Ellis Fischel Cancer Center - Columbia
Columbia, Missouri, 65203
Simmons Cancer Center - Dallas
Dallas, Texas, 75390
Veterans Affairs Medical Center - Atlanta (Decatur)
Decatur, Georgia, 30033
University of Colorado Cancer Center
Denver, Colorado, 80010
Dwight David Eisenhower Army Medical Center
Fort Gordon, Georgia, 30905-5650
Cancer Centers of the Carolinas
Greenville, South Carolina, 29615
Hackensack University Medical Center
Hackensack, New Jersey, 07601
Baylor College of Medicine
Houston, Texas, 77030
University of Kansas Medical Center
Kansas City, Kansas, 66160-7353
Norris Cotton Cancer Center
Lebanon, New Hampshire, 03756-0002
University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205
USC/Norris Comprehensive Cancer Center and Hospital
Los Angeles, California, 90033-0804
Jonsson Comprehensive Cancer Center, UCLA
Los Angeles, California, 90095-1781
Loyola University Medical Center
Maywood, Illinois, 60153
Oncology-Hematology Group of South Florida
Miami, Florida, 33176
Cancer Institute of New Jersey
New Brunswick, New Jersey, 08903
Tulane University School of Medicine
New Orleans, Louisiana, 70112
University of Nebraska Medical Center
Omaha, Nebraska, 68198-3330
University of Pennsylvania Cancer Center
Philadelphia, Pennsylvania, 19104-4283
Oregon Cancer Institute
Portland, Oregon, 97239
University of Rochester Medical Center
Rochester, New York, 14642-0001
Cancer Therapy and Research Center
San Antonio, Texas, 78229-3264
Louisiana State University Health Sciences Center - Shreveport
Shreveport, Louisiana, 71130-3932
About this study
Official title: Phase II Study of BAY 56-3722 in Patients With Recurrent, Unresectable, or Metastatic Renal Cell Carcinoma
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.
- Being tested
- BAY 56-3722, enzyme inhibitor therapy
- Medical subject headings
- Carcinoma, Renal Cell
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BAY 56-3722Drug
enzyme inhibitor therapyProcedure or surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jan 2003 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Stage IV Renal Cell CancerStudies of the same condition, open and under way.
- More trials run by Jonsson Comprehensive Cancer CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Jonsson Comprehensive Cancer Center
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Investigators
- Barbara J. Gitlitz, MD, Study chair, Jonsson Comprehensive Cancer Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00040989
- Sponsor's protocol ID
- UCLA-0201019
- Other IDs
- CDR0000069432, UTHSC-0125011152, BAYER-100364, NCI-G02-2090
- Status last verified
- Dec 2006
- First submitted
- 8 Jul 2002
- Last updated
- 10 Jul 2013
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Jul 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase II Study of BAY 56-3722 in Patients With Recurrent, Unresectable, or Metastatic Renal Cell Carcinoma
- ClinicalTrials.gov ID
- NCT00040989
- Acronym / sponsor ID
- UCLA-0201019
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Withdrawn
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Jonsson Comprehensive Cancer CenterUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- First posted
- 27 Jan 2003 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BAY 56-3722 | Drug | – |
| enzyme inhibitor therapy | Procedure or surgery | – |
Primary outcome
Not reported in the source record.
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jul 2013.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Barbara J. Gitlitz, MD study chair
Jonsson Comprehensive Cancer Center
26 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing BAY 56-3722 and enzyme inhibitor therapy in people with Stage IV Renal Cell Cancer and Recurrent Renal Cell Cancer, run by Jonsson Comprehensive Cancer Center at 26 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: withdrawn, as of the sponsor's last update on 10 Jul 2013. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 26 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jul 2013.