ConductScience.org, home

Trial · NCT03126110

Adverse events5,742

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal painGastrointestinal disordersPhase 1 Group B: INCAGN01876 1.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W151
otherAbdominal painGastrointestinal disordersPhase 1 Group B: INCAGN01876 3.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W040
otherAbdominal painGastrointestinal disordersPhase 1 Group B: INCAGN01876 5.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W040
otherAbdominal painGastrointestinal disordersPhase 1 Group C: INCAGN01876 1.0 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W040
otherAbdominal painGastrointestinal disordersPhase 1 Group C: INCAGN01876 3.0 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W181
otherAbdominal painGastrointestinal disordersPhase 1 Group C: INCAGN01876 5.0 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W030
otherAbdominal painGastrointestinal disordersPhase 1 Group D: INCAGN01876 + Nivolumab + Ipilimumab060
otherAbdominal painGastrointestinal disordersPhase 2 Group C2 PD-1/PD-L1 RM: INCAGN01876 300 mg + Ipilimumab 1 mg/kg181
otherAbdominal painGastrointestinal disordersPhase 2 Group F GC: INCAGN01876 300 mg + Nivolumab 240 mg3163
otherAbdominal painGastrointestinal disordersPhase 2 Group F SCCHN INCAGN01876 300 mg + Nivolumab 240 mg1461
otherAbdominal painGastrointestinal disordersPhase 2 Group F CC: INCAGN01876 300 mg + Nivolumab 240 mg6186
otherAbdominal painGastrointestinal disordersPhase 2 Group F PD-1/PD-L1 RM: INCAGN01876 300 mg + Nivolumab 240 mg040
otherAbdominal painGastrointestinal disordersPhase 2 Group F Biopsy: INCAGN01876 300 mg + Nivolumab 240 mg020
otherAbdominal painGastrointestinal disordersTotal1314513
otherAbdominal pain lowerGastrointestinal disordersPhase 1 Group A: INCAGN01876 1.0 mg/kg Q2W + Nivolumab 240 mg Q2W040
otherAbdominal pain lowerGastrointestinal disordersPhase 1 Group A: INCAGN01876 3.0 mg/kg Q2W + Nivolumab 240 mg Q2W040
otherAbdominal pain lowerGastrointestinal disordersPhase 1 Group A: INCAGN01876 5.0 mg/kg Q2W + Nivolumab 240 mg Q2W050
otherAbdominal pain lowerGastrointestinal disordersPhase 1 Group A: INCAGN01876 10.0 mg/kg Q2W + Nivolumab 240 mg Q2W040
otherAbdominal pain lowerGastrointestinal disordersPhase 1 Group B: INCAGN01876 1.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W050
otherAbdominal pain lowerGastrointestinal disordersPhase 1 Group B: INCAGN01876 3.0 mg/kg Q2W, Then Nivolumab 240 mg Q2W040

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

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03126110/events?page=3