ConductScience.org, home

Trial · NCT03499808

Results by group15

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

OutcomeGroupCategoryValueSpreadUnits
Assess Efficacy by Confirmed Overall Hematologic ResponseIsatuximab77.195% Confidence Interval 59.9 to 89.6percentage of paticipants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabAtrial fibrillation1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabFatigue1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabInfections and infestations - Other, specify1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabInfusion related reaction1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabLung infection2Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabLymphocyte count decreased3Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabPancreatitis1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabPruritus1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabSkin infection1Participants
To Evaluate Toxicities in the Treatment of Relapsed/Refractory AL Amyloidosis With Isatuximab.IsatuximabSyncope1Participants
Overall Survival (24 Month Estimate)Isatuximab8595% Confidence Interval 73 to 97percent of participants
Duration of Response (24 Month Estimate)Isatuximab8195% Confidence Interval 67 to 96Percent of Participants
Time to Hematologic ResponseIsatuximab1.195% Confidence Interval 1 to 3Months
Progression-free Survival (24 Month Estimate)Isatuximab7495% Confidence Interval 59 to 88percentage of paticipants

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03499808/results