Trial · NCT02100930
Anti-GD2 3F8 Monoclonal Antibody and GM-CSF for High-Risk Neuroblastoma
NCT02100930, Not applicable, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2020-02-28
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Anti-GD2 3F8 Monoclonal Antibody and GM-CSF for High-Risk Neuroblastoma. Trials, record NCT02100930. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02100930
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Anti-GD2 3F8 Monoclonal Antibody and GM-CSF for High-Risk Neuroblastoma
- NCT number
- NCT02100930
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 69 participants, actual
- Lead sponsor
- Memorial Sloan Kettering Cancer Center
- Conditions
- Neuroblastoma
- Interventions
- Anti-GD2 3F8 Monoclonal Antibody, GM-CSF (granulocyte-macrophage colony-stimulating factor), oral isotretinoin
- First posted
- 2014-04-01
- Last updated
- 2020-02-28
- Results first posted
- 2020-02-28
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Therapeutic Response | 2 years | Disease status is defined by the International Neuroblastoma Response Criteria - Complete response/remission (CR): NED; Partial response/remission: \>50% decrease in all disease parameters, exceptbone scan unchanged or improved; no more than 1 positive bone marrow site; Stable disease: \<50% decrease in all tumor markers; Progressive disease (PD): new lesion, or \>25 % increase in any disease marker. |
| Primary | Complete Remission | 2 years | Disease status is defined by the International Neuroblastoma Response Criteria - Complete response/remission (CR): NED; Partial response/remission: \>50% decrease in all disease parameters, exceptbone scan unchanged or improved; no more than 1 positive bone marrow site; Stable disease: \<50% decrease in all tumor markers; Progressive disease (PD): new lesion, or \>25 % increase in any disease marker. |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Therapeutic Response | 2 years | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Complete Remission | 2 years | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.gov
Results by group10
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Therapeutic Response | Neuroblastoma | No Evidence of Disease | 40 | Participants | |
| Therapeutic Response | Neuroblastoma | Complete Response | 3 | Participants | |
| Therapeutic Response | Neuroblastoma | Partial Response | 1 | Participants | |
| Therapeutic Response | Neuroblastoma | Stable Disease | 6 | Participants | |
| Therapeutic Response | Neuroblastoma | Progression of Disease | 19 | Participants | |
| Complete Remission | Neuroblastoma | No Evidence of Disease | 40 | Participants | |
| Complete Remission | Neuroblastoma | Complete Response | 3 | Participants | |
| Complete Remission | Neuroblastoma | Partial Response | 1 | Participants | |
| Complete Remission | Neuroblastoma | Stable Disease | 6 | Participants | |
| Complete Remission | Neuroblastoma | Progression of Disease | 19 | Participants |
Source ClinicalTrials.gov
Participant flow3
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Neuroblastoma | 69 | |
| Overall Study | COMPLETED | Neuroblastoma | 69 | |
| Overall Study | NOT COMPLETED | Neuroblastoma | 0 |
Source ClinicalTrials.gov
Adverse events58
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Edema face | General disorders | Neuroblastoma | 6 | 69 | |
| other | Pain | General disorders | Neuroblastoma | 6 | 69 | |
| other | Pruritus | Skin and subcutaneous tissue disorders | Neuroblastoma | 6 | 69 | |
| other | Urticaria | Skin and subcutaneous tissue disorders | Neuroblastoma | 6 | 69 | |
| other | Abdominal pain | Gastrointestinal disorders | Neuroblastoma | 5 | 69 | |
| other | Flushing | Vascular disorders | Neuroblastoma | 5 | 69 | |
| other | Pain in extremity | Musculoskeletal and connective tissue disorders | Neuroblastoma | 5 | 69 | |
| other | Vomiting | Gastrointestinal disorders | Neuroblastoma | 5 | 69 | |
| other | Agitation | Psychiatric disorders | Neuroblastoma | 4 | 69 | |
| other | Hypotension | Vascular disorders | Neuroblastoma | 4 | 69 |
1 to 10 of 58Source ClinicalTrials.gov
See all 58 adverse eventsAdverse event totals3
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Neuroblastoma | 16 | 69 |
| Total, other adverse events | Neuroblastoma | 69 | 69 |
| Total, serious adverse events | Neuroblastoma | 26 | 69 |
Source ClinicalTrials.gov
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/NCT02100930
GET https://conductscience.org/api/trials/v1/NCT02100930/events?page=2