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NCT03453255

DCHA as Postremission Therapy for AML With t(8;21)

Status unknown Phase 1, PHASE2 Last updated 5 March 2018
What this trial tests

Phase 1, PHASE2 trial testing Chemotherapy in Chemotherapy in 120 participants. Status unknown.

Timeline
1 January 2018
Primary endpoint
31 December 2019
31 December 2020

Quick facts

Lead sponsorChinese PLA General Hospital
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment120
Start date1 January 2018
Primary completion31 December 2019
Estimated completion31 December 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chinese PLA General Hospital

Who can join

Adults 14 to 65, any sex, with Chemotherapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Acute myelocytic leukemia ( AML) is a highly heterogeneous group of malignant hematopathy. Chromosomal translocation with t (8; 21) (q22; q22) , about 10 \~ 15% incidence in AML and 40% incidence in the AML-M2 type of leukemia, is a karyotype that is considered to have a good prognosis. The National Comprehensive Cancer Network (NCCN) guidelines recommend that high-dose Ara-c regimens may benefit for patients, but with 30 to 40% relapse and serious risks on myelosuppression, infection and bleeding in high-dose Ara-c consolidation chemotherapy and more than 70% recurrence rate with (tyrosine kinase)KIT mutation. So the exploration of a relatively safe and efficient consolidation therapy is one of the difficult problems to be solved in the treatment of mitigatory t (8; 21) AML.

Publications & conference data

4 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Therapeutic potential of tucidinostat, a subtype-selective HDAC inhibitor, in cancer treatment.
    Sun Y, Hong JH, Ning Z, Pan D, et al · · 2022 · cited 58× · PMID 36120308 · DOI 10.3389/fphar.2022.932914
  2. Emerging drugs targeting cellular redox homeostasis to eliminate acute myeloid leukemia stem cells.
    Costa RGA, Silva SLR, Dias IRSB, Oliveira MS, et al · · 2023 · cited 16× · PMID 37031536 · DOI 10.1016/j.redox.2023.102692
  3. Epigenetic modifications and targeted therapy in pediatric acute myeloid leukemia.
    Xu H, Wen Y, Jin R, Chen H. · · 2022 · cited 12× · PMID 36147798 · DOI 10.3389/fped.2022.975819
  4. Molecular Mechanisms of Senescence and Implications for the Treatment of Myeloid Malignancies.
    Ernst P, Heidel FH. · · 2021 · cited 8× · PMID 33557090 · DOI 10.3390/cancers13040612

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Other Chinese PLA General Hospital trials

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