HEC73543 Versus Salvage Chemotherapy in R/R FLT3-ITD AML

Recruiting Phase 3 Interventional Study
Leukemia, Acute Myeloid (AML)
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
324 (estimated)
Sponsor
Sunshine Lake Pharma Co., Ltd. · Industry
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About This Trial

A randomized,multicenter, open-label Phase III, clinical study is conducted to evaluate the clinical benefit Clifutinib in Chinese patients with relapsed/ refractory (R/R) FLT3-mutated AML as shown with overall survival compared to salvage chemotherapy, and also to investigate the efficacy of Clifutinib as assessed by CR/CRh rate in these subjects.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Subject is ≥ 18 years of age at the time of obtaining informed consent. * Subject has a diagnosis of primary acute myeloid leukemia (AML) or AML secondary to myelodysplastic syndrome (MDS) according to WHO classification; * Subject is refractory to or relapsed after first-line…
Contacts

Yingzhi Jiang, MSc

86 13692244182

jiangyingzhi@hec.cn

CONTACT