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Trial · NCT02973399

Efficacy and Safety of SNX-5422 Added to an Established Dose of Ibrutinib in CLL

NCT02973399, Phase 1, Terminated, Esanex Inc.

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Efficacy and Safety of SNX-5422 Added to an Established Dose of Ibrutinib in CLL. Trials, record NCT02973399. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02973399

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Trial

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

Title
Efficacy and Safety of SNX-5422 Added to an Established Dose of Ibrutinib in CLL
NCT number
NCT02973399
Status
Terminated
Phases
Phase 1
Enrollment
5 participants, actual
Lead sponsor
Esanex Inc.
Conditions
Cancer
Interventions
SNX-5422 plus ibrutinib
First posted
2016-11-25
Last updated
2019-02-22

Source ClinicalTrials.gov

Registered outcomes6

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

ListOutcomeTime frameDescription
PrimaryEfficacy of the combination of SNX-5422 and ibrutinib6 monthsProportion of subjects obtaining a complete response at the end of 6 SNX-5422 treatment cycles
SecondaryNumber of subjects reporting adverse eventsDay 28 of each 4 week cycle from randomization up to 52 weeksFrequency and severity of adverse events
SecondaryComplete response at 12 months12 monthsProportion of subjects obtaining a complete response at the end of 6 SNX-5422 treatment cycles
SecondaryImproved Clinical Status6 monthsProportion of subjects obtaining improvement in clinical status (i.e., Stable Disease becoming Partial Response) at the end of 6 SNX-5422 treatment cycles
SecondaryProgression free survival of patients receiving ibrutinib plus SNX-5422Up to 52 weeksElapsed time for each subject from randomization to continued survival up to 52 weeks
OtherBTK Mutation Level6 and 12 monthsChange from baseline in percent of CLL cells with Bruton's Tyrosine Kinase mutations at the end of 6 and 12 treatment cycles

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.

Grants0

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.

None in this release.

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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT02973399

GET https://conductscience.org/api/trials/v1/NCT02973399/registered