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An Efficacy Study of Milataxel (TL139) Administered Orally for Malignant Mesothelioma
Basic Trial Information Trial Description Summary Further Trial Information Eligibility Criteria Trial Contact Information
Basic Trial Information
Phase | Type | Status | Age | Protocol IDs |
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Phase II | Treatment | Active | 18 and over | TL139204 NCT00685204 |
Trial Description
Summary Milataxel is a new taxane that may have several advantages over the currently available taxanes. The current study is designed to determine the response rate of oral Milataxel in patients with malignant Mesothelioma. The study specifically targets patients who have recurring or progressive disease following previous chemotherapy. Further Study Information This is a non-randomized, multicenter, open label, single agent phase II study. Patients with malignant mesothelioma that has recurred or progressed following chemotherapy, and who qualify for this study, will receive milataxel 60 mg/m2 orally on Day 1 of a 21 day cycle. If no toxicities of greater than Grade 1 severity occur, patients will receive 75 mg/m2 for the second and subsequent cycles. Patients will receive drug for a total of six cycles. Milataxel administration in excess of six cycles will be permitted at the discretion of the Investigator if patients have stable or responding disease. Eligibility Criteria Inclusion Criteria: - Patients must have histologically or cytologically confirmed malignant mesothelioma for which they have received pemetrexed in combination with cisplatin as part of chemotherapeutic regimen.
- Prior cancer therapy with pemetrexed/cisplatin must have been completed at least 30 days prior to the first cycle of milataxel; prior radiotherapy (less than 25% of the bone marrow) must have been completed at least 30 days prior to study enrollment.
- Patients must have measurable disease by the Modified RECIST criteria
- Patients must have a life expectancy of at least 12 weeks and an ECOG performance status of 0, 1 or 2
- Patients must be 18 years of age.
- Patients must have adequate organ and system function.
- Patients must be able to comply with the protocol treatments and procedures.
- Patients with known brain metastases may be included in the study, providing they are clinically stable.
- Recovered from all acute toxicities caused by prior cancer therapies, except for alopecia.
Exclusion Criteria: - Patients must not have received any other chemotherapeutic treatment for malignant mesothelioma other than pemetrexed and a platinum agent such as cisplatin.
- Patients with grade 2 or greater peripheral neuropathy.
- Prior cancer therapies not completed within 30 days prior to the first cycle of milataxel; radiotherapy completed less than 30 days prior to study enrollment; patients not recovered from radiation-related toxicities; patients receiving any concurrent anti-cancer therapy, including trastuzumab, bevacizumab or an investigational agent while on-study; patients with greater than 2 prior radiotherapy treatments.
- Patients with known sensitivity to alcohol.
- Patients with significant intercurrent illnesses.
- Patients with symptomatic CNS metastases.
- Patients who have had major surgery within the past 14 days.
- Patients who require or are likely to require any strong modifier of CYP450 activity to be taken prior to milataxel administration
- Patients who are receiving high dose steroids (more than a dexamethasone-equivalent dose of 4 mg per day).
- Patients with malabsorption syndrome, disease significantly affecting gastrointestinal function, or major resection of the stomach or small bowel that could affect absorption of the study drug.
- Women who are pregnant or breastfeeding.
Trial Contact Information
Trial Lead Organizations/Sponsors Taxolog, Incorporated - New Jersey Harvey Pass, M.D. | | Principal Investigator |
Trial Sites
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U.S.A. |
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Illinois |
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Chicago |
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| Hedy L. Kindler | Principal Investigator |
| | | | | | | | | University of Chicago Cancer Research Center |
| | Sarah Mauro |
Ph: 773-834-3263 |
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Email:
smauro@medicine.bsd.uchicago.edu |
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New York |
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New York |
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| | | NYU Cancer Institute at New York University Medical Center |
| | Harvey Pass, M.D. |
Ph: 212-731-5414 |
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Email:
harvey.pass@med.nyu.edu |
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Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00685204 Information obtained from ClinicalTrials.gov on March 18, 2009 Note: Information about this trial is from the ClinicalTrials.gov database. The versions designated for health professionals and patients contain
the same text. Minor
changes may be made to the ClinicalTrials.gov record to standardize the names of study sponsors, sites, and
contacts. Cancer.gov only lists sites that are recruiting patients for active trials, whereas ClinicalTrials.gov lists all sites for all trials. Questions and comments regarding the presented information should
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