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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)

NCT01359982 Phase 1 COMPLETED Results posted

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 sponsorEpicentRx, Inc.
PhasePhase 1
StatusCOMPLETED
Enrolment26
Start date2011-09
Completion2015-02

Conditions

Interventions

Primary outcomes

Countries

United States