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Comparison · NCT02545907-8f145a22

Dose Level 0- Safety Population vs Dose Level 1- Safety Population: Compliance Profile of KTD Based on Reported Chemotherapy Compliance Data.

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Dose Level 0- Safety Population vs Dose Level 1- Safety Population: Compliance Profile of KTD Based on Reported Chemotherapy Compliance Data. Trial comparisons, record NCT02545907-8f145a22. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02545907-8f145a22

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3330.06150.792wilson
Risk in group 20.7140.3590.918wilson
Risk difference, group 1 minus group 2-0.381-0.7210.2newcombe hybrid score
Risk ratio, group 1 over group 20.4670.08812.47log
Odds ratio, group 1 over group 20.20.01093.66log
Number needed to treat, for one fewer participant with the outcome on Dose Level 0- Safety Population than on Dose Level 1- Safety Population2.62from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Dose Level 0- Safety PopulationAll patients allocated to dose level 0 that received at least one dose of Carfilzomib and with no protocol deviations with relevant impact on safety will be included in the safety analysis set.13OG000
Group 2Dose Level 1- Safety PopulationAll patients allocated to dose level 1 that received at least one dose of Carfilzomib and with no protocol deviations with relevant impact on safety will be included in the safety analysis set.57OG001

Outcome

Type
SECONDARY
Title
Compliance Profile of KTD Based on Reported Chemotherapy Compliance Data.
Description
The compliant profile of participants to KTD will be assessed by determining the number of missed doses from recorded data. Participants will be regarded as compliant if participants have missed no more than 14 days of thalidomide, 2 days of dexamethasone, and 1 dose of carfilzomib per cycle. Compliance will be reported in terms of the number of participants who were compliant.
Time frame
Within 6 months
Population

Source ClinicalTrials.gov

Trial

Title
A Dose Escalation Study of Carfilzomib Taken With Thalidomide and Dexamethasone in Relapsed AL Amyloidosis
NCT number
NCT02545907
Phases
PHASE1, PHASE2
Conditions
Amyloidosis
Interventions
Carfilzomib, Thalidomide, Dexamethasone
Lead sponsor
University College, London
Results first posted
2021-04-15

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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