Comparison · NCT01419665-6dcd2614
GP2013 vs Rituximab: To Evaluate the Overall Survival (OS) With up to 3 Years of Follow-up Post Randomization, as Assessed by the Number of Deaths
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. GP2013 vs Rituximab: To Evaluate the Overall Survival (OS) With up to 3 Years of Follow-up Post Randomization, as Assessed by the Number of Deaths. Trial comparisons, record NCT01419665-6dcd2614. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01419665-6dcd2614
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0929 | 0.0655 | 0.13 | wilson | |
| Risk in group 2 | 0.0984 | 0.0702 | 0.136 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00546 | -0.0523 | 0.0413 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.944 | 0.584 | 1.53 | log | |
| Odds ratio, group 1 over group 2 | 0.939 | 0.551 | 1.6 | log | |
| Number needed to treat, for one fewer participant with the outcome on GP2013 than on Rituximab | 183 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | GP2013 | Experimental Type: Biological/Vaccine | 29 | 312 | OG000 |
| Group 2 | Rituximab | Comparator Type: Biological/Vaccine | 31 | 315 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- To Evaluate the Overall Survival (OS) With up to 3 Years of Follow-up Post Randomization, as Assessed by the Number of Deaths
- Description
OS was defined as the time from date of randomization to date of death due to any cause. If a patient was not known to have died, OS was censored at the date of last contact including survival follow-up.
- Time frame
- 3 years
- Population
- per protocol set, participants with measure
Source ClinicalTrials.gov
Trial
- Title
- GP2013 in the Treatment of Patients With Previously Untreated, Advanced Stage Follicular Lymphoma (ASSIST_FL)
- NCT number
- NCT01419665
- Phases
- PHASE3
- Conditions
- Follicular Lymphoma
- Interventions
- GP2013, rituximab
- Lead sponsor
- Sandoz
- Results first posted
- 2021-05-14
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01419665?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
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
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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