Trial · NCT03126110
Adverse event totals54
The totals the trial posted for each group.
1 to 20 of 54
Download this page as JSON| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Phase 1 Group A: INCAGN01876 1.0 mg/kg Q2W + Nivolumab 240 mg Q2W | 2 | 4 |
| Total, all-cause mortality | Phase 1 Group A: INCAGN01876 3.0 mg/kg Q2W + Nivolumab 240 mg Q2W | 2 | 4 |
| Total, all-cause mortality | Phase 1 Group A: INCAGN01876 5.0 mg/kg Q2W + Nivolumab 240 mg Q2W | 4 | 5 |
| Total, all-cause mortality | Phase 1 Group A: INCAGN01876 10.0 mg/kg Q2W + Nivolumab 240 mg Q2W | 3 | 4 |
| Total, all-cause mortality | Phase 1 Group B: INCAGN01876 1.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W | 4 | 5 |
| Total, all-cause mortality | Phase 1 Group B: INCAGN01876 3.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W | 4 | 4 |
| Total, all-cause mortality | Phase 1 Group B: INCAGN01876 5.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W | 3 | 4 |
| Total, all-cause mortality | Phase 1 Group C: INCAGN01876 1.0 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W | 4 | 4 |
| Total, all-cause mortality | Phase 1 Group C: INCAGN01876 3.0 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W | 5 | 8 |
| Total, all-cause mortality | Phase 1 Group C: INCAGN01876 5.0 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W | 2 | 3 |
| Total, all-cause mortality | Phase 1 Group D: INCAGN01876 + Nivolumab + Ipilimumab | 6 | 6 |
| Total, all-cause mortality | Phase 2 Group C2 PD-1/PD-L1 RM: INCAGN01876 300 mg + Ipilimumab 1 mg/kg | 6 | 8 |
| Total, all-cause mortality | Phase 2 Group F GC: INCAGN01876 300 mg + Nivolumab 240 mg | 12 | 16 |
| Total, all-cause mortality | Phase 2 Group F SCCHN INCAGN01876 300 mg + Nivolumab 240 mg | 25 | 46 |
| Total, all-cause mortality | Phase 2 Group F CC: INCAGN01876 300 mg + Nivolumab 240 mg | 11 | 18 |
| Total, all-cause mortality | Phase 2 Group F PD-1/PD-L1 RM: INCAGN01876 300 mg + Nivolumab 240 mg | 3 | 4 |
| Total, all-cause mortality | Phase 2 Group F Biopsy: INCAGN01876 300 mg + Nivolumab 240 mg | 2 | 2 |
| Total, all-cause mortality | Total | 98 | 145 |
| Total, other adverse events | Phase 1 Group A: INCAGN01876 1.0 mg/kg Q2W + Nivolumab 240 mg Q2W | 4 | 4 |
| Total, other adverse events | Phase 1 Group A: INCAGN01876 3.0 mg/kg Q2W + Nivolumab 240 mg Q2W | 4 | 4 |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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
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GET https://conductscience.org/api/trials/v1/NCT03126110/event-totals