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Trial · NCT03703297

Results by group20

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Durvalumab Versus Placebo: Progression-Free Survival (PFS) Assessed by Blinded Independent Central Review (BICR) Per Response Evaluation Criteria in Solid Tumors Version 1.1Durvalumab16.695% Confidence Interval 10.2 to 28.2months
Durvalumab Versus Placebo: Progression-Free Survival (PFS) Assessed by Blinded Independent Central Review (BICR) Per Response Evaluation Criteria in Solid Tumors Version 1.1Placebo9.295% Confidence Interval 7.4 to 12.9months
Durvalumab Versus Placebo: Overall Survival (OS)Durvalumab55.995% Confidence Interval 37.3 to NAmonths
Durvalumab Versus Placebo: Overall Survival (OS)Placebo33.495% Confidence Interval 25.5 to 39.9months
Durvalumab Versus Placebo: Objective Response Rate (ORR) Assessed by Blinded Independent Central Review Per Response Evaluation Criteria in Solid Tumors Version 1.1Durvalumab30.3percentage of participants
Durvalumab Versus Placebo: Objective Response Rate (ORR) Assessed by Blinded Independent Central Review Per Response Evaluation Criteria in Solid Tumors Version 1.1Placebo32.0percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Progression-Free at 18 Months Following Randomization (PFS18) Assessed by Blinded Independent Central Review Per Response Evaluation Criteria in Solid Tumors Version 1.1
Durvalumab48.895% Confidence Interval 42.2 to 55.0percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Progression-Free at 18 Months Following Randomization (PFS18) Assessed by Blinded Independent Central Review Per Response Evaluation Criteria in Solid Tumors Version 1.1
Placebo36.195% Confidence Interval 29.9 to 42.2percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Progression-Free at 24 Months Following Randomization (PFS24) Assessed by Blinded Independent Central Review Per Response Evaluation Criteria in Solid Tumors Version 1.1
Durvalumab46.295% Confidence Interval 39.6 to 52.5percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Progression-Free at 24 Months Following Randomization (PFS24) Assessed by Blinded Independent Central Review Per Response Evaluation Criteria in Solid Tumors Version 1.1
Placebo34.295% Confidence Interval 28.2 to 40.3percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Alive at 24 Months From Randomization (OS24)Durvalumab68.095% Confidence Interval 61.9 to 73.3percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Alive at 24 Months From Randomization (OS24)Placebo58.595% Confidence Interval 52.3 to 64.3percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Alive at 36 Months From Randomization (OS36)Durvalumab56.595% Confidence Interval 50.0 to 62.5percentage of participants
Durvalumab Versus Placebo: Percentage of Participants Alive at 36 Months From Randomization (OS36)Placebo47.695% Confidence Interval 41.3 to 53.7percentage of participants
Durvalumab: Serum Concentration of DurvalumabDurvalumabCycle 1 Day 1: End of infusion431.00Standard Deviation 327.861microgram per milliliter (mcg/mL)
Durvalumab: Serum Concentration of DurvalumabDurvalumabCycle 2 (Week 4): Pre-infusion89.57Standard Deviation 107.228microgram per milliliter (mcg/mL)
Durvalumab: Serum Concentration of DurvalumabDurvalumabCycle 5 (Week 16): Pre-infusion159.63Standard Deviation 58.561microgram per milliliter (mcg/mL)
Durvalumab: Serum Concentration of DurvalumabDurvalumabCycle 26 (Week 100): Pre-infusion178.20Standard Deviation 65.422microgram per milliliter (mcg/mL)
Durvalumab: Serum Concentration of DurvalumabDurvalumabMonth 3 follow-up44.97Standard Deviation 36.026microgram per milliliter (mcg/mL)
Durvalumab: Number of Participants With Anti-Drug Antibody (ADA) Response to DurvalumabDurvalumab7Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license 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.

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