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Trial · NCT02545907

Results by group41

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Dose-Limiting Toxicities as Assessed by Reported DataDose Level 00Participants
Number of Participants With Dose-Limiting Toxicities as Assessed by Reported DataDose Level 11Participants
Number of Participants Experiencing Grade 3 or 4 Toxicity as Assessed by CTCAE v4.0.Dose Level 0- Safety Population2Participants
Number of Participants Experiencing Grade 3 or 4 Toxicity as Assessed by CTCAE v4.0.Dose Level 1- Safety Population3Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 0- Safety PopulationWithin 3 cycles1Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 1- Safety PopulationWithin 3 cycles5Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 0- Safety PopulationAt the end of cycle 31Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 1- Safety PopulationAt the end of cycle 35Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 0- Safety PopulationWithin 6 cycles2Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 1- Safety PopulationWithin 6 cycles5Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 0- Safety PopulationAt the end of cycle 62Participants
Clonal Response Rate Within 3 Months, at 3 Months, Within 6 Months and at 6 Months as Determined by Paraprotein and Free Light Chain Assessment.Dose Level 1- Safety PopulationAt the end of cycle 65Participants
Amyloidotic Organ Response Rate Within 3 Months and 6 Months Based on Biochemical, Electrocardiographical, and Radiographical Assessment.Dose Level 0- Safety PopulationResponse within 3 months0Participants
Amyloidotic Organ Response Rate Within 3 Months and 6 Months Based on Biochemical, Electrocardiographical, and Radiographical Assessment.Dose Level 1- Safety PopulationResponse within 3 months0Participants
Amyloidotic Organ Response Rate Within 3 Months and 6 Months Based on Biochemical, Electrocardiographical, and Radiographical Assessment.Dose Level 0- Safety PopulationResponse within 6 months0Participants
Amyloidotic Organ Response Rate Within 3 Months and 6 Months Based on Biochemical, Electrocardiographical, and Radiographical Assessment.Dose Level 1- Safety PopulationResponse within 6 months0Participants
Amyloidotic Organ Response Rate Within 3 Months and 6 Months Based on Biochemical, Electrocardiographical, and Radiographical Assessment.Dose Level 0- Safety PopulationNo response3Participants
Amyloidotic Organ Response Rate Within 3 Months and 6 Months Based on Biochemical, Electrocardiographical, and Radiographical Assessment.Dose Level 1- Safety PopulationNo response7Participants
Time to Amyloidotic Organ Response Based on Reported Data.Dose Level 0- Safety Population0Participants
Time to Amyloidotic Organ Response Based on Reported Data.Dose Level 1- Safety Population0Participants

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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