Trial · NCT03599960
Combination Chemotherapy in Patients With Newly Diagnosed BPDCN
NCT03599960, Phase 2, Unknown, Centre Hospitalier Universitaire de Besancon
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Combination Chemotherapy in Patients With Newly Diagnosed BPDCN. Trials, record NCT03599960. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03599960
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Combination Chemotherapy in Patients With Newly Diagnosed BPDCN
- NCT number
- NCT03599960
- Status
- Unknown
- Phases
- Phase 2
- Enrollment
- 26 participants, actual
- Lead sponsor
- Centre Hospitalier Universitaire de Besancon
- Conditions
- Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)
- Interventions
- Chemotherapy
- First posted
- 2018-07-26
- Last updated
- 2024-02-08
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Proportion of patients with complete response after 3 cycles of chemotherapy | 12 weeks (3 weeks after 3 cycles of chemotherapy (each cycle is 21 days)) | Proportion of patients with complete response after 3 cycles of chemotherapy |
| Secondary | Proportion of patients with response (complete or partial) after 3 cycles of chemotherapy | 12 weeks (3 weeks after 3 cycles of chemotherapy (each cycle is 21 days)) | Proportion of patients with response (complete or partial) after 3 cycles of chemotherapy |
| Secondary | Overall survival | 24 months | Overall survival |
| Secondary | Relapse-free survival | 24 months | Relapse-free survival |
| Secondary | Residual L-asparaginase activity | 12 weeks (Day 8 of each chemotherapy cycle (each cycle is 21 days)) | Residual L-asparaginase activity |
| Secondary | Anti-L-asparaginase antibodies levels | 12 weeks (Day 8 of each chemotherapy cycle (each cycle is 21 days)) | Evaluation of the titer of the anti-asparaginase antibody |
| Other | Minimal residual disease analysis | 24 months | presence of PDC cell blast (CD56 +, NG2 +, BDCA2low, BDCA4low, CD123low, cTCL1high as measured by flow cytometry) |
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/NCT03599960
GET https://conductscience.org/api/trials/v1/NCT03599960/registered