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NCT03239145 · OUTCOME

Overall Survival at 1 Year (OS1)

Pembrolizumab (Anti-PD-1) and AMG386 (Angiopoietin-2 (Ang-2) in Patients With Advanced Solid Tumor · Source last updated 2026-07-01

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
NUMBER
Unit
percentage of participants
Interval / dispersion
90% Confidence Interval
Time frame
1 year

What was measured

OS1 is the percent probability estimate at 1 year based on the Kaplan-Meier method. OS is defined as the time from or registration to death due to any cause, or censored at date last known alive.

Analysis population: The analysis population will include patients enrolled in the dose escalation and dose expansion portions of the trial. Per protocol, the dose escalation and dose expansion data may be combined for patients with the same cancer type who received the same treatment doses.

Groups in this outcome

[Dose Level II] Pembrolizumab + Trebananib (Colorectal)

Participants received pembrolizumab 200 mg administered intravenously every 3 weeks in combination with trebananib administered intravenously at 30 mg/kg weekly.

[Dose Level II] Pembrolizumab + Trebananib (Ovarian)

Participants received pembrolizumab 200 mg administered intravenously every 3 weeks in combination with trebananib administered intravenously at 30 mg/kg weekly.

[Dose Level II] Pembrolizumab + Trebananib (Renal Cell Carcinoma)

Participants received pembrolizumab 200 mg administered intravenously every 3 weeks in combination with trebananib administered intravenously at 30 mg/kg weekly.

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

Analysis denominator · Participants

GroupSource count
[Dose Level II] Pembrolizumab + Trebananib (Colorectal)40
[Dose Level II] Pembrolizumab + Trebananib (Ovarian)11
[Dose Level II] Pembrolizumab + Trebananib (Renal Cell Carcinoma)4

Reported measurements

Source class 1
Values in percentage of participants · Interval/dispersion: 90% Confidence Interval
GroupValueSpreadLowerUpperComment
[Dose Level II] Pembrolizumab + Trebananib (Colorectal)45Not reported2861Not reported
[Dose Level II] Pembrolizumab + Trebananib (Ovarian)80Not reported3895Not reported
[Dose Level II] Pembrolizumab + Trebananib (Renal Cell Carcinoma)50Not reported684Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        28
        upper Limit
        61
        value
        45
      2. group Id
        OG001
        lower Limit
        38
        upper Limit
        95
        value
        80
      3. group Id
        OG002
        lower Limit
        6
        upper Limit
        84
        value
        50
denoms
  1. counts
    1. group Id
      OG000
      value
      40
    2. group Id
      OG001
      value
      11
    3. group Id
      OG002
      value
      4
    units
    Participants
description
OS1 is the percent probability estimate at 1 year based on the Kaplan-Meier method. OS is defined as the time from or registration to death due to any cause, or censored at date last known alive.
dispersion Type
90% Confidence Interval
groups
  1. description
    Participants received pembrolizumab 200 mg administered intravenously every 3 weeks in combination with trebananib administered intravenously at 30 mg/kg weekly.
    id
    OG000
    title
    [Dose Level II] Pembrolizumab + Trebananib (Colorectal)
  2. description
    Participants received pembrolizumab 200 mg administered intravenously every 3 weeks in combination with trebananib administered intravenously at 30 mg/kg weekly.
    id
    OG001
    title
    [Dose Level II] Pembrolizumab + Trebananib (Ovarian)
  3. description
    Participants received pembrolizumab 200 mg administered intravenously every 3 weeks in combination with trebananib administered intravenously at 30 mg/kg weekly.
    id
    OG002
    title
    [Dose Level II] Pembrolizumab + Trebananib (Renal Cell Carcinoma)
param Type
NUMBER
population Description
The analysis population will include patients enrolled in the dose escalation and dose expansion portions of the trial. Per protocol, the dose escalation and dose expansion data may be combined for patients with the same cancer type who received the same treatment doses.
reporting Status
POSTED
time Frame
1 year
title
Overall Survival at 1 Year (OS1)
type
SECONDARY
unit Of Measure
percentage of participants

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice