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MechanismCOX-2 inhibitors |
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Drug Highest PhasePhase 1 |
First Approval Ctry. / Loc.- |
First Approval Date- |
A Phase 1 Open-Label, Multiple Dose, Two Part Dose Escalation Study of ECP-1014 as a Treatment for Patients With Solid Tumor Cancers
The primary objective of this study is to evaluate the safety, tolerability, pharmacokinetics, and optimal recommended Phase 2 dose (RP2D) during a 28-day dosing period of ECP-1014 in patients with solid tumors and by evaluation of dose limiting toxicities.
100 Clinical Results associated with Euclises Pharmaceuticals, Inc.
0 Patents (Medical) associated with Euclises Pharmaceuticals, Inc.
100 Deals associated with Euclises Pharmaceuticals, Inc.
100 Translational Medicine associated with Euclises Pharmaceuticals, Inc.