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NCT03356080
DLAAG in the Treatment of Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome With Blast Excess
Phase 2 trial testing Decitabine in Acute Myeloid Leukemia in 50 participants. Status unknown.
7 July 2019
Quick facts
| Lead sponsor | Shanghai Tong Ren Hospital |
|---|---|
| Phase | Phase 2 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 50 |
| Start date | 7 July 2017 |
| Primary completion | 7 July 2019 |
| Estimated completion | 7 July 2020 |
| Sites | 6 locations across China |
Drugs / interventions tested
- Decitabine (decitabine) — full drug profile →
- Cytarabine — full drug profile →
- All-transretinoic acid — full drug profile →
- G-CSF (g-csf) — full drug profile →
Conditions studied
- Acute Myeloid Leukemia — all drugs for Acute Myeloid Leukemia →
- Myelodysplastic Syndrome — all drugs for Myelodysplastic Syndrome →
Sponsor
Shanghai Tong Ren Hospital
Who can join
Adults 18 to 90, any sex, with Acute Myeloid Leukemia or Myelodysplastic Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to evaluate of the clinical efficacy and safety of DLAAG protocol in the treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome with blast excess
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine.
Ferreira R, Napoli J, Enver T, Bernardino L, et al · · 2020 · cited 81× · PMID 32848154 · DOI 10.1038/s41467-020-18042-2 -
Hypomethylating Agents and Immunotherapy: Therapeutic Synergism in Acute Myeloid Leukemia and Myelodysplastic Syndromes.
Wong KK, Hassan R, Yaacob NS. · · 2021 · cited 38× · PMID 33718188 · DOI 10.3389/fonc.2021.624742 -
All-trans retinoic acid in hematologic disorders: not just acute promyelocytic leukemia.
Chen Y, Tong X, Lu R, Zhang Z, et al · · 2024 · cited 16× · PMID 39027338 · DOI 10.3389/fphar.2024.1404092 -
The AML immune paradox: decoding escape pathways and pioneering checkpoint, vaccine, and combination strategies.
Soleimani Samarkhazan H, Shafiei FS, Taghinejad Z, Maleknia M, et al · · 2025 · cited 14× · PMID 40634759 · DOI 10.1007/s10238-025-01795-9 -
Historical expectations with DNA methyltransferase inhibitor monotherapy in MDS: when is combination therapy truly "promising"?
Brunner AM, Fell G, Steensma DP. · · 2022 · cited 3× · PMID 35143613 · DOI 10.1182/bloodadvances.2021006357
Verify or expand the search:
- PubMed search for NCT03356080
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Other Shanghai Tong Ren Hospital trials
Trials by the same sponsor.
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- NCT06508541 — The Prognosis of Colorectal Cancer Patients After Indocyanine Green Fluorescence-guided Radical Surgery · completed
- NCT05736978 — Adaptive Treatment for Acute Myeloid Leukemia Based on D14 MRD Results · Phase 2 · recruiting
- NCT05736965 — A Study of Selinexor in Combination With Azacitidine and Venetoclax (SAV Regimen) in Treatment Naïve Participants With A · Phase 2 · recruiting
- NCT05526300 — Intelligent Hypertension Intervention Study · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03356080 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Shanghai Tong Ren Hospital
- Last refreshed: 29 November 2017
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03356080.
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