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A Phase I, Open-Label, Multiple Ascending Dose Study to Assess the Safety, Tolerability and Pharmacokinetics of RRx-001 in Subjects With Advanced Solid Tumors or Lymphomas For Which There Are No Currently Accepted Curative Therapies (DINAMIC)
The purpose of this study is to evaluate the safety and pharmacokinetic profile of RRx-001 for injection in subjects with advanced solid tumors or lymphomas for which there are no currently accepted curative therapies. This study will also conduct an exploratory evaluation of objective tumor response using CT or MRI.
Details
| Lead sponsor | EpicentRx, Inc. |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 26 |
| Start date | 2011-09 |
| Completion | 2015-02 |
Conditions
- Malignant Solid Tumor
- Lymphomas
Interventions
- RRx-001
- RRx-001
- RRx-001
- RRx-001
- RRx-001
- RRx-001
Primary outcomes
- Number of Patients Who Had an Adverse Events — From time of receiving a dose of RRx-001 through 92 days
The total number of patients who experienced at least one adverse event while receiving treatment.
Countries
United States