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Trial · NCT03820817

Rifaximin in Patients With Monoclonal Gammopathy

NCT03820817, Phase 1, Completed, Emory University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Rifaximin in Patients With Monoclonal Gammopathy. Trials, record NCT03820817. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03820817

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Rifaximin in Patients With Monoclonal Gammopathy
NCT number
NCT03820817
Status
Completed
Phases
Phase 1
Enrollment
50 participants, actual
Lead sponsor
Emory University
Conditions
IgA Monoclonal Gammopathy, IgG Monoclonal Gammopathy, IgM Monoclonal Gammopathy, Light Chain Deposition Disease, Monoclonal Gammopathy, Smoldering Waldenstrom Macroglobulinemia, Waldenstrom Macroglobulinemia, Gammopathy, Monoclonal, Gammopathy Igg
Interventions
Rifaximin
First posted
2019-01-29
Last updated
2026-05-26

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryClinical response rate defined as a reduction in clonal immunoglobulin (Ig) by > 25%Up to 2 weeks after study startClinical response rate will be calculated as proportion (responders/total patients).
SecondaryIncidence of adverse events graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 4.0Up to 12 weeks after study start
Incidence of adverse events (AEs) occurring during the study will be summarized by system organ class and preferred term. Adverse events will also be summarized by causality and grade. Serious adverse events will be listed separately.
SecondaryChanges in stool microbiotaUp to 12 weeks after study start16S sequencing will be used to compare changes in stool microbiota.
SecondaryChanges in gammopathyUp to 12 weeks after study startChanges in clonal Ig will be used to assess changes in gammopathy.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

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

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
P30CA138292Winship Cancer Institute Cancer Center Support GrantRAMALINGAM, SURESH SEMORY UNIVERSITYNATIONAL CANCER INSTITUTE2009 to 2025

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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 trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03820817

GET https://conductscience.org/api/trials/v1/NCT03820817/registered