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Active Org.- |
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Active Indication- |
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Drug Highest PhaseDiscontinued |
First Approval Ctry. / Loc.- |
First Approval Date- |
Phase 1 OL, Dose Escalating, Multiple Dose Study To Determine The Safety, Tolerability, MTD, And Pharmacokinetics Of MPC-2130 Administered As Daily IV Infusions For 5 Days, Repeated Every 21 Days, In Patients With Refractory Cancer
Phase 1 Open-label treatment with MPC-2130 for subjects with refractory cancer.
100 Clinical Results associated with Myriad Therapeutics, Inc.
0 Patents (Medical) associated with Myriad Therapeutics, Inc.
100 Deals associated with Myriad Therapeutics, Inc.
100 Translational Medicine associated with Myriad Therapeutics, Inc.