Trial · NCT03564704
Precision Diagnosis Directing HDACi Chidamide Target Therapy for Adult T-LBL/ALL
NCT03564704, Phase 2, Phase 3, Unknown, Nanfang Hospital, Southern Medical University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Precision Diagnosis Directing HDACi Chidamide Target Therapy for Adult T-LBL/ALL. Trials, record NCT03564704. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03564704
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Precision Diagnosis Directing HDACi Chidamide Target Therapy for Adult T-LBL/ALL
- NCT number
- NCT03564704
- Status
- Unknown
- Phases
- Phase 2, Phase 3
- Enrollment
- 80 participants, estimated
- Lead sponsor
- Nanfang Hospital, Southern Medical University
- Conditions
- Leukemia, Leukemia, Acute, Adult Lymphoblastic Lymphoma, Leukemia, Lymphoblastic, Leukemia, T Cell, Adult Acute Lymphoblastic Leukemia, Lymphoblastic Lymphoma, Lymphoblastic Leukemia
- Interventions
Dexamethasone, vincristine, Cyclophosphamide, Idarubicin, Pegaspargase, Adriamycin, Methotrexate, 6-mercaptopurine., Etoposide, Cytarabine, Bone marrow aspiration, Intrathecal injection, Radiation therapy, NGS, allogeneic hematopoietic stem cell transplantation, Flow-MRD, FISH, Flow immunophenotyping, Karyotyping, Chidamide, PET-CT scan
- First posted
- 2018-06-21
- Last updated
- 2018-06-21
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Event-Free-Survival | 3 years | 3 years EFS of LBL/ALL patients enrolled in PDT-ALL-LBL |
| Secondary | Minimum residual disease after induction | 3 months | MRD after induction regimen of PDT-ALL-LBL protocol |
| Secondary | CR after Induction Therapy | 3 months | CR after induction regimen of PDT-ALL-LBL protocol |
| Secondary | Death in induction | 3 months | Dearth during induction regimen of PDT-ALL-LBL |
| Secondary | Adverse events | 3 years | AE of 3 years of LBL patients enrolled in PDT-ALL-LBL |
| Secondary | Relapse | 3 years | Cumulative incidence relapse rate of 3 years of LBL patients enrolled in PDT-ALL-LBL protocol |
| Secondary | Relapse free survival | 3 years | 3 years RFS of LBL patients enrolled in PDT-ALL-LBL protocol |
| Secondary | Overall survival | 3 years | 3 years OS of LBL patients enrolled in PDT-ALL-LBL protocol |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03564704
GET https://conductscience.org/api/trials/v1/NCT03564704/registered