Trial · NCT04236141
Results by group76
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 76
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
Percentage of Participants With Complete Response (CR) at the End of Treatment (EOT) Assessment Based on Positron Emission Tomography-Computed Tomography (PET-CT) Assessed by Independent Review Committee (IRC) | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 25.0 | 95% Confidence Interval 10.69 to 44.87 | percentage of participants | |
Percentage of Participants With Complete Response (CR) at the End of Treatment (EOT) Assessment Based on Positron Emission Tomography-Computed Tomography (PET-CT) Assessed by Independent Review Committee (IRC) | Placebo Plus Bendamustine and Rituximab | 14.3 | 95% Confidence Interval 1.78 to 42.81 | percentage of participants | |
| Percentage of Participants With CR at the EOT Assessment Based on PET-CT as Assessed by Investigator | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 21.4 | 95% Confidence Interval 8.30 to 40.95 | percentage of participants | |
| Percentage of Participants With CR at the EOT Assessment Based on PET-CT as Assessed by Investigator | Placebo Plus Bendamustine and Rituximab | 14.3 | 95% Confidence Interval 1.78 to 42.81 | percentage of participants | |
| Percentage of Participants With Objective Response (OR) at EOT Based on PET-CT as Assessed by Investigator | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 28.6 | 95% Confidence Interval 13.22 to 48.67 | percentage of participants | |
| Percentage of Participants With Objective Response (OR) at EOT Based on PET-CT as Assessed by Investigator | Placebo Plus Bendamustine and Rituximab | 14.3 | 95% Confidence Interval 1.78 to 42.81 | percentage of participants | |
| Percentage of Participants With OR at EOT Based on PET-CT as Assessed by IRC | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 35.7 | 95% Confidence Interval 18.64 to 55.93 | percentage of participants | |
| Percentage of Participants With OR at EOT Based on PET-CT as Assessed by IRC | Placebo Plus Bendamustine and Rituximab | 14.3 | 95% Confidence Interval 1.78 to 42.81 | percentage of participants | |
| Percentage of Participants With CR at EOT Based on Computed Tomography (CT) as Assessed by Investigator | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 17.9 | 95% Confidence Interval 6.06 to 36.89 | percentage of participants | |
| Percentage of Participants With CR at EOT Based on Computed Tomography (CT) as Assessed by Investigator | Placebo Plus Bendamustine and Rituximab | 0 | 95% Confidence Interval 0.00 to 23.16 | percentage of participants | |
| Percentage of Participants With CR at EOT Based on CT as Assessed by IRC | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 17.9 | 95% Confidence Interval 6.06 to 36.89 | percentage of participants | |
| Percentage of Participants With CR at EOT Based on CT as Assessed by IRC | Placebo Plus Bendamustine and Rituximab | 0 | 95% Confidence Interval 0.00 to 23.16 | percentage of participants | |
| Percentage of Participants With OR at EOT Assessment Based on CT as Assessed by Investigator | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 32.1 | 95% Confidence Interval 15.88 to 52.35 | percentage of participants | |
| Percentage of Participants With OR at EOT Assessment Based on CT as Assessed by Investigator | Placebo Plus Bendamustine and Rituximab | 14.3 | 95% Confidence Interval 1.78 to 42.81 | percentage of participants | |
| Percentage of Participants With OR at EOT Assessment Based on CT as Assessed by IRC | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 28.6 | 95% Confidence Interval 13.22 to 48.67 | percentage of participants | |
| Percentage of Participants With OR at EOT Assessment Based on CT as Assessed by IRC | Placebo Plus Bendamustine and Rituximab | 14.3 | 95% Confidence Interval 1.78 to 42.81 | percentage of participants | |
| Percentage of Participants With Best Overall Response (BOR) Based on PET-CT or CT Only as Assessed by Investigator | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 53.6 | 95% Confidence Interval 33.87 to 72.49 | percentage of participants | |
| Percentage of Participants With Best Overall Response (BOR) Based on PET-CT or CT Only as Assessed by Investigator | Placebo Plus Bendamustine and Rituximab | 28.6 | 95% Confidence Interval 8.39 to 58.10 | percentage of participants | |
| Percentage of Participants With Best Overall Response (BOR) Based on PET-CT or CT Only as Assessed by IRC | Polatuzumab Vedotin Plus Bendamustine and Rituximab | 53.6 | 95% Confidence Interval 33.87 to 72.49 | percentage of participants | |
| Percentage of Participants With Best Overall Response (BOR) Based on PET-CT or CT Only as Assessed by IRC | Placebo Plus Bendamustine and Rituximab | 50.0 | 95% Confidence Interval 23.04 to 76.96 | percentage of participants |
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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GET https://conductscience.org/api/trials/v1/NCT04236141/results