NCT05185947 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- All-Cause Mortality was monitored/assessed an average of 5.60 months. Adverse Events were monitored/assessed Day-4 through completion of surveillance post-treatment, up to 2 years.
- Other-event reporting threshold
- 0%
"Participants Enrolled, and Assigned to an Arm/Cohort, But Not Treated", and "Participants Enrolled, Not Assigned to an Arm/Cohort and Not Treated" are excluded in the table because only treated participants were assessed for death and adverse events.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Intravenous Paclitaxel Dose Level 1, Intraperitoneal Paclitaxel Dose Level 1, Nilotinib Dose Level 1 | 2 / 4 | 4 / 4 | 4 / 4 |
| Intravenous Paclitaxel DoseLevel -1, Intraperitoneal Paclitaxel Dose Level 1, Nilotinib Dose Level 1 | 0 / 1 | 1 / 1 | 0 / 1 |
| Intravenous Paclitaxel DoseLevel 1, Intraperitoneal Paclitaxel Dose Level 1, Nilotinib Dose Level -1 | 1 / 1 | 1 / 1 | 1 / 1 |
| Intravenous Paclitaxel DoseLevel -1, Intraperitoneal Paclitaxel DoseLevel 1, Nilotinib Dose Level -1 | 0 / 1 | 1 / 1 | 1 / 1 |
Serious adverse events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Respiratory, thoracic and mediastinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Hypoxia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Vascular disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Thromboembolic event
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Infections and infestations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Peritoneal infection
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Infections and infestations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Sepsis
Other reported adverse events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Gastrointestinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Abdominal pain
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Blood and lymphatic system disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 10
- term
- Anemia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Metabolism and nutrition disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Anorexia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Cardiac disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Atrial fibrillation
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Investigations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 3
- term
- Blood bilirubin increased
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Gastrointestinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Constipation
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Investigations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Creatinine increased
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Metabolism and nutrition disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Dehydration
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Gastrointestinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 2
- term
- Diarrhea
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Nervous system disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Dizziness
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Nervous system disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Dysgeusia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- General disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 2
- term
- Edema limbs
Complete source fields
- description
- "Participants Enrolled, and Assigned to an Arm/Cohort, But Not Treated", and "Participants Enrolled, Not Assigned to an Arm/Cohort and Not Treated" are excluded in the table because only treated participants were assessed for death and adverse events.
- event Groups
- deaths Num Affected
- 4
- deaths Num At Risk
- 4
- description
- Ended treatment at the regular dose level: 80 intravenous (IV)/80 Intraperitoneal (IP) + 300 twice a day (BID).
- id
- EG000
- other Num Affected
- 4
- other Num At Risk
- 4
- serious Num Affected
- 2
- serious Num At Risk
- 4
- title
- Intravenous Paclitaxel Dose Level 1, Intraperitoneal Paclitaxel Dose Level 1, Nilotinib Dose Level 1
- deaths Num Affected
- 0
- deaths Num At Risk
- 1
- description
- Had the planned doses for Intraperitoneal (IP) Paclitaxel (80 IP) and by mouth (PO) nilotinib (300 twice a day (BID) but declined to go up to the 80mg/m\^2 of intravenous (IV) Paclitaxel.
- id
- EG001
- other Num Affected
- 1
- other Num At Risk
- 1
- serious Num Affected
- 0
- serious Num At Risk
- 1
- title
- Intravenous Paclitaxel DoseLevel -1, Intraperitoneal Paclitaxel Dose Level 1, Nilotinib Dose Level 1
- deaths Num Affected
- 1
- deaths Num At Risk
- 1
- description
- Had the planned doses for intravenous (IV) and Intraperitoneal (IP) Paclitaxel (80 IV/80 IP) but had a dose reduction for Nilotinib (400 every day (QD).
- id
- EG002
- other Num Affected
- 1
- other Num At Risk
- 1
- serious Num Affected
- 1
- serious Num At Risk
- 1
- title
- Intravenous Paclitaxel DoseLevel 1, Intraperitoneal Paclitaxel Dose Level 1, Nilotinib Dose Level -1
- deaths Num Affected
- 1
- deaths Num At Risk
- 1
- description
- Had the planned dose of Intraperitoneal (IP) Paclitaxel (80 IP) but had a dose reduction for intravenous (IV) Paclitaxel (60 IV), and a dose reduction for Nilotinib (400 every day (QD).
- id
- EG003
- other Num Affected
- 1
- other Num At Risk
- 1
- serious Num Affected
- 0
- serious Num At Risk
- 1
- title
- Intravenous Paclitaxel DoseLevel -1, Intraperitoneal Paclitaxel DoseLevel 1, Nilotinib Dose Level -1
- frequency Threshold
- 0
- other Events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Gastrointestinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Abdominal pain
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Blood and lymphatic system disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 10
- term
- Anemia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Metabolism and nutrition disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Anorexia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Cardiac disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Atrial fibrillation
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Investigations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 3
- term
- Blood bilirubin increased
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Gastrointestinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Constipation
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Investigations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Creatinine increased
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Metabolism and nutrition disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Dehydration
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Gastrointestinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 2
- term
- Diarrhea
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Nervous system disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- term
- Dizziness
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Nervous system disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Dysgeusia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- General disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 1
- num At Risk
- 1
- num Events
- 2
- term
- Edema limbs
- serious Events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Respiratory, thoracic and mediastinal disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Hypoxia
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Vascular disorders
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Thromboembolic event
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Infections and infestations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 0
- num At Risk
- 4
- num Events
- 0
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 1
- num At Risk
- 1
- num Events
- 1
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Peritoneal infection
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Infections and infestations
- source Vocabulary
- CTCAE (5.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 4
- num Events
- 1
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG002
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- group Id
- EG003
- num Affected
- 0
- num At Risk
- 1
- num Events
- 0
- term
- Sepsis
- time Frame
- All-Cause Mortality was monitored/assessed an average of 5.60 months. Adverse Events were monitored/assessed Day-4 through completion of surveillance post-treatment, up to 2 years.
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