CLINICAL TRIALS PROFILE FOR TEW-7197
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Clinical Trials for TEW-7197
Trial ID | Title | Status | Sponsor | Phase | Summary |
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NCT02160106 ↗ | First in Human Dose Escalation Study of Vactosertib (TEW-7197) in Subjects With Advanced Stage Solid Tumors | Completed | National OncoVenture | Phase 1 | The phase I dose escalation study will investigate the safety, tolerability, and pharmacokinetics of the TGF-β pathway inhibitor TEW 7197 in subjects with advanced, refractory solid tumors. |
NCT02160106 ↗ | First in Human Dose Escalation Study of Vactosertib (TEW-7197) in Subjects With Advanced Stage Solid Tumors | Completed | MedPacto, Inc. | Phase 1 | The phase I dose escalation study will investigate the safety, tolerability, and pharmacokinetics of the TGF-β pathway inhibitor TEW 7197 in subjects with advanced, refractory solid tumors. |
NCT03074006 ↗ | Dose Escalation and Proof-of-Concept Studies of Vactosertib (TEW-7197) Monotherapy in Patients With MDS | Completed | MedPacto, Inc. | Phase 1 | This is a prospective, open-label, multicenter, phase 1/2 study of TEW-7197 in patients with low and intermediate risk of myelodysplastic syndrome (MDS). |
NCT03143985 ↗ | Vactosertib in Combination w/ Pomalidomide in Relapsed or Relapsed and Refractory Multiple Myeloma | Recruiting | Case Comprehensive Cancer Center | Phase 1 | The purpose of this study is to see if the study drug, called Vactosertib, is safe and determine what the best dose is to treat future patients when given in combination with pomalidomide (POM). The study will also look to see if it has any effect on multiple myeloma, when given in combination with POM. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for TEW-7197
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Clinical Trial Sponsors for TEW-7197
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