NCT01693562 · OUTCOME
Number of Participants With Abnormal Vital Signs Reported as TEAEs in the Dose-escalation, Dose-exploration, and Dose-expansion Phase
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- From Day 1 through 90 days after the last dose of study drug (approximately 5.25 years)
What was measured
Number of participants with abnormal vital signs reported as TEAEs are reported. Abnormal vital signs are defined as any abnormal finding in the vital sign parameters (body weight, body temperature, blood pressure, pulse rate, and respiratory rate).
Analysis population: As-treated population included all participants who received any dose of study drug. Participants enrolled in the 10 mg/kg Q2W Expansion and Escalation Cohort have been summarized as a total only. This is because the safety profile of durvalumab monotherapy 10 mg/kg Q2W was manageable and generally consistent with the known safety profile of the anti-PD-L1/PD-1 drug class.
Groups in this outcome
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)
Participants received intravenous (IV) infusion of MEDI4736 (durvalumab) 0.1 mg/kg every 2 weeks (Q2W) in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)
Participants received IV infusion of MEDI4736 0.3 mg/kg Q2W in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation , whichever occurred first
Escalation Cohort (MEDI4736 1 mg/kg Q2W)
Participants received IV infusion of MEDI4736 1 mg/kg Q2W in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
Escalation Cohort (MEDI4736 3 mg/kg Q2W)
Participants received IV infusion of MEDI4736 3 mg/kg Q2W in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation , whichever occurred first.
Escalation Cohort (MEDI4736 15 mg/kg Q3W)
Participants received IV infusion of MEDI4736 15 mg/kg every 3 weeks (Q3W) in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
Exploration Cohort (MEDI4736 20 mg/kg Q4W)
Participants received IV infusion of MEDI4736 20 mg/kg every 4 weeks (Q4W) in the dose-exploration phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)
Participants received IV infusion of MEDI4736 10 mg/kg Q2W in the dose-escalation or dose-expansion phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation , whichever occurred first.
| Group | Source count |
|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 4 |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 4 |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 3 |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 3 |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 7 |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 21 |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 980 |
Reported measurements
Pyrexia
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 3 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 1 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 3 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 2 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 145 | Not reported | Not reported | Not reported | Not reported |
Weight decreased
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 2 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 79 | Not reported | Not reported | Not reported | Not reported |
Hypertension
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 1 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 1 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 31 | Not reported | Not reported | Not reported | Not reported |
Hypotension
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 1 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 36 | Not reported | Not reported | Not reported | Not reported |
Weight increased
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 22 | Not reported | Not reported | Not reported | Not reported |
Tachycardia
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 19 | Not reported | Not reported | Not reported | Not reported |
Sinus tachycardia
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 14 | Not reported | Not reported | Not reported | Not reported |
Arrhythmia
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 3 | Not reported | Not reported | Not reported | Not reported |
Sinus bradycardia
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 3 | Not reported | Not reported | Not reported | Not reported |
Heart rate increased
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 1 | Not reported | Not reported | Not reported | Not reported |
Heart rate irregular
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 1 | Not reported | Not reported | Not reported | Not reported |
Peak expiratory flow rate decreased
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Escalation Cohort (MEDI4736 0.1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 0.3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 1 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 3 mg/kg Q2W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation Cohort (MEDI4736 15 mg/kg Q3W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Exploration Cohort (MEDI4736 20 mg/kg Q4W) | 0 | Not reported | Not reported | Not reported | Not reported |
| Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W) | 1 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 3
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 1
- group Id
- OG004
- value
- 3
- group Id
- OG005
- value
- 2
- group Id
- OG006
- value
- 145
- title
- Pyrexia
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 2
- group Id
- OG006
- value
- 79
- title
- Weight decreased
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 1
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 1
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 31
- title
- Hypertension
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 1
- group Id
- OG006
- value
- 36
- title
- Hypotension
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 22
- title
- Weight increased
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 19
- title
- Tachycardia
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 14
- title
- Sinus tachycardia
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 3
- title
- Arrhythmia
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 3
- title
- Sinus bradycardia
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 1
- title
- Heart rate increased
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 1
- title
- Heart rate irregular
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 1
- title
- Peak expiratory flow rate decreased
- denoms
- counts
- group Id
- OG000
- value
- 4
- group Id
- OG001
- value
- 4
- group Id
- OG002
- value
- 3
- group Id
- OG003
- value
- 3
- group Id
- OG004
- value
- 7
- group Id
- OG005
- value
- 21
- group Id
- OG006
- value
- 980
- units
- Participants
- description
- Number of participants with abnormal vital signs reported as TEAEs are reported. Abnormal vital signs are defined as any abnormal finding in the vital sign parameters (body weight, body temperature, blood pressure, pulse rate, and respiratory rate).
- groups
- description
- Participants received intravenous (IV) infusion of MEDI4736 (durvalumab) 0.1 mg/kg every 2 weeks (Q2W) in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
- id
- OG000
- title
- Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)
- description
- Participants received IV infusion of MEDI4736 0.3 mg/kg Q2W in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation , whichever occurred first
- id
- OG001
- title
- Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)
- description
- Participants received IV infusion of MEDI4736 1 mg/kg Q2W in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
- id
- OG002
- title
- Escalation Cohort (MEDI4736 1 mg/kg Q2W)
- description
- Participants received IV infusion of MEDI4736 3 mg/kg Q2W in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation , whichever occurred first.
- id
- OG003
- title
- Escalation Cohort (MEDI4736 3 mg/kg Q2W)
- description
- Participants received IV infusion of MEDI4736 15 mg/kg every 3 weeks (Q3W) in the dose-escalation phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
- id
- OG004
- title
- Escalation Cohort (MEDI4736 15 mg/kg Q3W)
- description
- Participants received IV infusion of MEDI4736 20 mg/kg every 4 weeks (Q4W) in the dose-exploration phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation, whichever occurred first.
- id
- OG005
- title
- Exploration Cohort (MEDI4736 20 mg/kg Q4W)
- description
- Participants received IV infusion of MEDI4736 10 mg/kg Q2W in the dose-escalation or dose-expansion phase for maximum of 12 months or until confirmed progressive disease, initiation of alternative cancer therapy, unacceptable toxicity, withdrawal of consent, or development of other reason for treatment discontinuation , whichever occurred first.
- id
- OG006
- title
- Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- As-treated population included all participants who received any dose of study drug. Participants enrolled in the 10 mg/kg Q2W Expansion and Escalation Cohort have been summarized as a total only. This is because the safety profile of durvalumab monotherapy 10 mg/kg Q2W was manageable and generally consistent with the known safety profile of the anti-PD-L1/PD-1 drug class.
- reporting Status
- POSTED
- time Frame
- From Day 1 through 90 days after the last dose of study drug (approximately 5.25 years)
- title
- Number of Participants With Abnormal Vital Signs Reported as TEAEs in the Dose-escalation, Dose-exploration, and Dose-expansion Phase
- type
- PRIMARY
- unit Of Measure
- Participants
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