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clinical trials overview | completed glioma clinical trials | active studies
TM601-003 – Phase I imaging study of intravenous 131I-TM601 in patients with recurrent or refractory metastatic tumors Qualified patients with confirmed recurrent or refractory metastatic tumors will receive escalating doses of IV This study is no longer recruiting patients.
This study is enrolling patients with confirmed recurrent and/or progressive malignant glioma to evaluate the safety and efficacy of multiple intravenously administered doses of This study is active, but not yet recruiting patients.
TM601-011 - A Phase 1/2, Multi-Center, Safety and Efficacy Study Evaluating Intravenously Administered 131I-TM601 in Patients with Progressive and/or Recurrent Malignant Melanoma. Qualified patients with confirmed progressive and/or recurrent malignant Melanoma will be receive multiple doses of intravenously administered This study is active, but not yet recruiting patients.
TM601-007 – Phase I dose escalating study evaluating the safety and biologically active dose of TM601 based on perfusion MRI imaging criteria in patients with progressive and/or recurrent malignant glioma Qualified patients with confirmed progressive and/or recurrent malignant glioma that demonstrate tumor specific uptake of TM601 will receive intravenous infusions at one of six dose levels once a week for 3 weeks. Patients will be enrolled in successive dose cohorts until either a Maximum Tolerated Dose (MTD) is defined, or perfusion changes have been demonstrated in 5 out of 6 patients in a cohort. This study is currently recruiting patients.
For more information, prospective patients or their physicians should contact Amy Bock, TransMolecular's Senior Director, Clinical Operations at 617-995-3050 x 316 or by email at bock@transmolecular.com More information about TransMolecular clinical trials active studies patients can also be found at the following websites: Clinical trials.gov Emerging Medicine Virtual Trials
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