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最高研发阶段临床1期 |
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非在研适应症- |
最高研发阶段临床前 |
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非在研适应症- |
最高研发阶段临床前 |
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A Phase I, First in Human, Open-label Study of Escalating Doses of INA03 Administered Intravenously as Single Agent in Adult Patients With Relapse/Refractory Acute Leukemia
This Phase 1 Study is an open-label, non-randomized, dose escalation, safety, efficacy, pharmacokinetic, and pharmacodynamic evaluation study of INA03 administered as a single agent IV infusion every 2 weeks to patients ≥18 years of age with R/R AML, MLL, or ALL.
The study will be performed in 2 parts: a Dose Titration for Day 1 study (Part 1) followed by a Dose Escalation Part (Part 2) of INA03 used as monotherapy.
100 项与 Inatherys SAS 相关的临床结果
0 项与 Inatherys SAS 相关的专利(医药)
100 项与 Inatherys SAS 相关的药物交易
100 项与 Inatherys SAS 相关的转化医学