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NCT01693562 · OUTCOME

Number of Participants With Abnormal Vital Signs Reported as TEAEs in the Dose-escalation, Dose-exploration, and Dose-expansion Phase

A Phase 1/2 Study to Evaluate MEDI4736 · Source last updated 2021-05-13

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 identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource 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
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)3Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)1Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)3Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)2Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)145Not reportedNot reportedNot reportedNot reported
Weight decreased
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)2Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)79Not reportedNot reportedNot reportedNot reported
Hypertension
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)1Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)1Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)31Not reportedNot reportedNot reportedNot reported
Hypotension
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)1Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)36Not reportedNot reportedNot reportedNot reported
Weight increased
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)22Not reportedNot reportedNot reportedNot reported
Tachycardia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)19Not reportedNot reportedNot reportedNot reported
Sinus tachycardia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)14Not reportedNot reportedNot reportedNot reported
Arrhythmia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)3Not reportedNot reportedNot reportedNot reported
Sinus bradycardia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)3Not reportedNot reportedNot reportedNot reported
Heart rate increased
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)1Not reportedNot reportedNot reportedNot reported
Heart rate irregular
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)1Not reportedNot reportedNot reportedNot reported
Peak expiratory flow rate decreased
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Escalation Cohort (MEDI4736 0.1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 0.3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 1 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 3 mg/kg Q2W)0Not reportedNot reportedNot reportedNot reported
Escalation Cohort (MEDI4736 15 mg/kg Q3W)0Not reportedNot reportedNot reportedNot reported
Exploration Cohort (MEDI4736 20 mg/kg Q4W)0Not reportedNot reportedNot reportedNot reported
Escalation/Expansion Cohort (Total MEDI4736 10 mg/kg Q2W)1Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        3
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        1
      5. group Id
        OG004
        value
        3
      6. group Id
        OG005
        value
        2
      7. group Id
        OG006
        value
        145
    title
    Pyrexia
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        2
      7. group Id
        OG006
        value
        79
    title
    Weight decreased
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        1
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        31
    title
    Hypertension
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        1
      7. group Id
        OG006
        value
        36
    title
    Hypotension
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        22
    title
    Weight increased
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        19
    title
    Tachycardia
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        14
    title
    Sinus tachycardia
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        3
    title
    Arrhythmia
  9. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        3
    title
    Sinus bradycardia
  10. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        1
    title
    Heart rate increased
  11. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        1
    title
    Heart rate irregular
  12. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        1
    title
    Peak expiratory flow rate decreased
denoms
  1. counts
    1. group Id
      OG000
      value
      4
    2. group Id
      OG001
      value
      4
    3. group Id
      OG002
      value
      3
    4. group Id
      OG003
      value
      3
    5. group Id
      OG004
      value
      7
    6. group Id
      OG005
      value
      21
    7. 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
  1. 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)
  2. 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)
  3. 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)
  4. 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)
  5. 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)
  6. 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)
  7. 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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Preserved source evidence · Not medical advice