PHASE II OPEN-LABEL SAFETY EXTENSION STUDY OF TANEZUMAB IN CANCER PATIENTS WITH PAIN DUE TO BONE METASTASES
- Conditions
- PAIN DUE TO BONE METASTASESMedDRA version: 9.1Level: LLTClassification code 10049038Term: Metastatic bone pain
- Registration Number
- EUCTR2008-005182-66-FR
- Lead Sponsor
- Pfizer Inc 235 East 42nd Street New York, NY 10017
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 58
1. The patient must consent in writing to participate in the study by signing and dating an informed consent document indicating that the patient has been informed of all pertinent aspects of the study prior to conducting any study-related procedures.
2. The patient met the eligibility criteria for, and was randomized and treated with intravenous study drug in Study A4091003.
3. At least 8 weeks but no more than 16 weeks has elapsed since the intravenous study drug infusion in Study A4091003.
4. Female patients must meet one of the following criteria:
a. Female patients of non-childbearing potential: must be post menopausal, defined as women who are = 45 years old with amenorrhea for 24 consecutive months (regardless of FSH levels at Study A4091003 Screening) or women who are amenorrheic for at least 1 year AND have a serum follicle stimulating hormone (FSH) level greater than 30 IU/L at Study A4091003 Screening; or be surgically sterile, defined as having had a hysterectomy and/or bilateral oophorectomy;
b. Female patients of child bearing potential: must not be pregnant or lactating and must be abstinent or use adequate contraception (2 forms of birth control, one of which must be a barrier method) from Baseline visit until 16 weeks after the last dose of study medication. Women of childbearing potential must have a negative erum pregnancy test at Study A4091003 Termination Visit or a negative urine regnancy test at Baseline prior to initial dosing.
Male patients must agree that they and their female spouses/partners will use adequate contraception (2 forms of birth control, one of which must be barrier method) or be of non childbearing potential.
In the event of indeterminate or anomalous results on pregnancy/FSH testing or issues surrounding contraceptive requirements, study management should be contacted and will make the final decision as to the adequacy/need for contraception.
5. The patient has a Karnofsky Performance Score =40% at Baseline;
6. The patient has an anticipated life expectancy of =6 months at Baseline;
7. The patient must be willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Patients presenting with any of the following will not enter the study:
1. The patient was withdrawn from Study A4091003 for an adverse event or serious adverse event.
2. Use of any investigational medication within 30 days prior to Baseline or plans to receive an investigational medication other than the study medication during the course of this study.
3. Patients who discontinued Study A4091003 prior to Week 8 because of lack of compliance, protocol violation, not meeting entrance criteria, withdrawal of consent, disease progression or patients who were lost to follow up will be excluded from Study A4091029.
4. Occurrence of any adverse event or condition during Study A4091003 or since termination from that study that, in the opinion of the Investigator, would put the patient at increased safety risk or should exclude the subject from participating in the open-label extension.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method