Comparison · NCT02730299-fa7826bc
NiCord® (Omidubicel) vs Unmanipulated CBU(s): Number of Participants With Platelet Engraftment by 42 Days Post-transplantation
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. NiCord® (Omidubicel) vs Unmanipulated CBU(s): Number of Participants With Platelet Engraftment by 42 Days Post-transplantation. Trial comparisons, record NCT02730299-fa7826bc. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02730299-fa7826bc
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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 | 0.548 | 0.425 | 0.666 | wilson | |
| Risk in group 2 | 0.349 | 0.243 | 0.472 | wilson | |
| Risk difference, group 1 minus group 2 | 0.199 | 0.025 | 0.357 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.57 | 1.05 | 2.36 | log | |
| Odds ratio, group 1 over group 2 | 2.26 | 1.1 | 4.65 | log | |
| Number needed to treat, for one more participant with the outcome on NiCord® (Omidubicel) than on Unmanipulated CBU(s) | 5.02 | 2.8 | 40 | from the risk difference interval |
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 | NiCord® (Omidubicel) | NiCord® is a cryopreserved stem/progenitor cell based product comprised of:~1. ex vivo expanded, umbilical cord blood-derived hematopoietic CD34+ progenitor cells (NiCord® cultured fraction (CF))~2. the non-cultured cell fraction of the same Cord Blood Unit (CBU) (NiCord® Non-cultured Fraction (NF)) consisting of mature myeloid and lymphoid cells.~Both fractions, i.e. NiCord® CF and NiCord® NF, will be kept frozen until they are thawed and infused on the day of transplantation.~NiCord® (omidubicel) | 34 | 62 | OG000 |
| Group 2 | Unmanipulated CBU(s) | Unmanipulated cord blood unit(s) | 22 | 63 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Platelet Engraftment by 42 Days Post-transplantation
- Description
Platelet engraftment defined as the first day of a minimum of three consecutive measurements on different days such that the patient has achieved a platelet count \> 20 × 10\^9/L with no platelet transfusions during the preceding seven days (counting day of engraftment as one of the preceding seven days) for the Intent to Treat Population
- Time frame
- 42 days post-transplantation
- Population
- Intent to Treat Population
Source ClinicalTrials.gov
Trial
- Title
- Stem Cell Transplantation With NiCord® (Omidubicel) vs Standard UCB in Patients With Leukemia, Lymphoma, and MDS
- NCT number
- NCT02730299
- Phases
- PHASE3
- Conditions
- Hematological Malignancies, Acute Lymphoblastic Leukemia (ALL), Acute Myelogenous Leukemia (AML), Chronic Myelogenous Leukemia (CML), Myelodysplastic Syndrome (MDS), Lymphoma, Acute Leukemia
- Interventions
- NiCord® (omidubicel), Cord Blood Unit
- Lead sponsor
- Gamida Cell ltd
- Results first posted
- 2022-10-25
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02730299?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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