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在研机构- |
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在研适应症- |
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最高研发阶段终止 |
首次获批国家/地区- |
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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.
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