Phase I Study of Patupilone and RAD001
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Purpose
This is an unblinded, dose escalation study of patupilone in combination with RAD001 in subjects with advanced cancer to find the maximum tolerated dose of each drug. The purpose of this study is to see what doses of RAD001 and patupilone are safe to use when the two drugs are used at the same time. Other goals in this study are to learn about the effect of RAD 001 and patupilone on tumor growth; to find out what amount of RAD001 is present in the blood when it is combined with patupilone; to learn about proteins in the blood that may predict or show an effect of RAD001 or patupilone and to learn if any changes are seen in the tumor with the type of test called a PET scan.Subjects will be assigned to a dosing group. The dose of patupilone and RAD001 a subject gets depends on when they enter onto this study. The initial subjects in the study will take the lowest doses of RAD001 and patupilone. At least 3 subjects will be treated in each dosing group starting with the smallest dose. If there are few or easy to handle side effects, the next group of at least 3 people to enter in the study will get the next higher dose. This continues until the highest dose of the study drug is found that does not cause serious or hard to treat side effects. Both the subjects and the study doctor will know which dose is assigned. In this study, RAD001 will be given as tablets to take with water. RAD001 will be taken for either 7, 14, or 21 days of each 21 day cycle depending on which dosing group is assigned. If taking RAD 001 and patupilone on the same day, then RAD 001 will be taken with water however prior to receiving patupilone.Patupilone will be given by an intravenous injection (through a vein) for 20 minutes on Days 1 or day 6 of the 21-day cycle. The patupilone dose will be based on height and weight. Blood tests (approximately 1-3 teaspoons) will be done every week. Every six weeks a CT scan or MRI will be done to assess the tumor size. Subjects will continue to receive RAD001 and patupilone as long as the tumor is stable or shrinking, and not having too many side effects from treatment.
| Condition | Intervention | Phase |
|---|---|---|
|
Refractory Malignancy |
Drug: Patupilone Drug: RAD001 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase I Study of Patupilone and RAD001 in Patients With Refractory Solid Tumor Malignancy |
- To identify the maximum tolerated doses (MTD) of the combination of patupilone and RAD001 [ Time Frame: 3 years ] [ Designated as safety issue: No ]
- find toxicity of patupilone and RAD001, see if concentrations of RAD001 are elevated with patupilone, evaluate tumor response using standard imaging, develop pharmacodynamic markers that may predict/indicate response to mTOR inhibition or patupilone trt [ Time Frame: 3 years ] [ Designated as safety issue: No ]
| Enrollment: | 42 |
| Study Start Date: | July 2007 |
| Study Completion Date: | February 2011 |
| Primary Completion Date: | February 2011 (Final data collection date for primary outcome measure) |
-
Drug: Patupilone
Primary Endpoint To identify the maximum tolerated doses (MTD) of the combination of patupilone and RAD001
Secondary Endpoints To assess the toxicity of patupilone and RAD001 To determine if concentrations of RAD001 are elevated in the presence of patupilone To evaluate tumor response using standard imaging modalities (CT scan, x-ray, bone scan) To develop pharmacodynamic markers that may predict or indicate response to mTOR inhibition or patupilone treatment.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- All patients must have malignancy refractory to standard therapy or for whom no standard, effective therapy is available.
- Patient must have performance status 0-2 on the ECOG Performance Status (see Appendix B)
- Patient's disease must be measurable (RECIST) or evaluable (e.g., cytologically or radiologically detectable disease such as ascites, peritoneal deposits, or lesions which do not fulfill RECIST criteria for measurable disease).
- Patients must have intact intestinal absorption
- Patients must have adequate organ function
- Patient must have recovered from toxicity of prior chemotherapy and/or radiotherapy. Patient may not have received chemotherapy in the prior 4 weeks. Patients may have not received radiotherapy in the prior 3 weeks.
- Patient (male or female) must be ≥ 18 years old.
- Women must not be pregnant or lactating. Female patients of childbearing potential must have a negative pregnancy test within 7 days before initiation of study drug dosing. Post menopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential. Male and female patients of reproductive potential must agree to employ an effective barrier method of birth control throughout the study, and for three months following discontinuation of study drug.
- Signed written informed consent.
Exclusion Criteria:
- Patient has received greater than 3 prior cytotoxic regimens for metastatic disease.
- Prior therapy with epothilones, rapamycin, rapamycin analogs, or known sensitivity to these agents
- Prior treatment with any investigational drug within the preceding 4 weeks.
- Patient has history of bone marrow or stem cell transplant.
- Patient has received prior radiation therapy to greater than 25% of the bone marrow.
- Patients has newly diagnosed, not yet treated or uncontrolled brain metastases or leptomeningeal disease.
- Patient has known hypersensitivity to the components of study drugs or its analogs.
- Patient with known Grade 3 or 4 hypersensitivity to macrolide antibiotics (eg. clarithromycin, erythromycin, azithromycin).
- Patient with any active (acute or chronic) or uncontrolled infection requiring systemic therapy.
- Patients with chronic treatment with systemic steroids or another immunosuppressive agent
- Patient with known HIV infection.
- Patients with unresolved diarrhea within the last 7 days prior to start of treatment.
- Concomitant treatment with medications that are listed as clinically relevant inducers or inhibitors of cytochrome P450 (CYP3A).
- Patients taking Coumadin® or other agents containing warfarin, with the exception of low dose Coumadin® (1 mg or less) administered prophylactically for maintenance of in-dwelling lines or ports
- Herbal preparations or related over-the-counter preparations containing herbal ingredients (eg. St. John's Wort)
- Any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study such as: unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤ 6 months prior to first study treatment, serious uncontrolled cardiac arrhythmia, or severely impaired lung function
- Any patient with uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN
- Any patient with nonmalignant medical illnesses that are uncontrolled or whose control may be jeopardized by the treatment with the study therapy
- Patients with liver disease such as cirrhosis, chronic active hepatitis, or chronic persistent hepatitis
- Patients receiving immunization with attenuated live vaccines during study participation.
Contacts and Locations| United States, New Jersey | |
| The Cancer Institute of New Jersey | |
| New Brunswick, New Jersey, United States, 08901 | |
| Principal Investigator: | Mark Stein, MD | University of Medicine and Dentistry New Jersey |
More Information
No publications provided
| Responsible Party: | University of Medicine and Dentistry New Jersey |
| ClinicalTrials.gov Identifier: | NCT00496600 History of Changes |
| Other Study ID Numbers: | 050612, CRAD001US16, 0220060307 |
| Study First Received: | July 3, 2007 |
| Last Updated: | June 13, 2012 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Neoplasms Sirolimus Everolimus Epothilone B Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Antifungal Agents |
Anti-Infective Agents Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Anti-Bacterial Agents Tubulin Modulators Antimitotic Agents Mitosis Modulators Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 16, 2013