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Trial · NCT02061085

Monotherapy With Eribulin In Her2 Negative Metastatic Breast Cancer as a First Line Treatment

NCT02061085, Phase 2, Completed, MedSIR; results first posted 2025-06-08

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Monotherapy With Eribulin In Her2 Negative Metastatic Breast Cancer as a First Line Treatment. Trials, record NCT02061085. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02061085

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Trial

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

Title
Monotherapy With Eribulin In Her2 Negative Metastatic Breast Cancer as a First Line Treatment
NCT number
NCT02061085
Status
Completed
Phases
Phase 2
Enrollment
53 participants, actual
Lead sponsor
MedSIR
Conditions
Breast Neoplasm, Metastasis
Interventions
Eribulin
First posted
2014-02-12
Last updated
2025-06-08
Other registries' IDs
eudract:2012-004463-41
Results first posted
2025-06-08

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryTime to ProgressionThrough study completion, up to 27 monthsPer Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0)
SecondaryDuration of ResponseThrough study completion, up to 27 monthsDuration of response
SecondaryClinical Benefit RateThrough study completion, up to 27 months
SecondaryProgression Free SurvivalThrough study completion, up to 27 months

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTime to ProgressionThrough study completion, up to 27 monthsmonthsMEDIAN
SECONDARYDuration of ResponseThrough study completion, up to 27 monthsmonthsMEDIAN
SECONDARYClinical Benefit RateThrough study completion, up to 27 monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProgression Free SurvivalThrough study completion, up to 27 monthsMonthsMEDIAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Time to ProgressionMonotherapy Treatment With Eribulin4.195% Confidence Interval 3.2 to 6.6months
Duration of ResponseMonotherapy Treatment With Eribulin4.5Full Range 2.1 to 20.9months
Clinical Benefit RateMonotherapy Treatment With Eribulin14Participants
Progression Free SurvivalMonotherapy Treatment With Eribulin4.195% Confidence Interval 3.2 to 6.6Months

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMonotherapy Treatment With Eribulin53
Overall StudyCOMPLETEDMonotherapy Treatment With Eribulin45
Overall StudyNOT COMPLETEDMonotherapy Treatment With Eribulin8

Adverse events27

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherNeuropathy peripheralNervous system disordersMonotherapy Treatment With Eribulin105310
otherDry mouthGeneral disordersMonotherapy Treatment With Eribulin4534
otherNauseaGastrointestinal disordersMonotherapy Treatment With Eribulin145314
otherConstipationGastrointestinal disordersMonotherapy Treatment With Eribulin105310
otherAnorexia and bulimia syndromeGastrointestinal disordersMonotherapy Treatment With Eribulin105310
otherAbdominal painGastrointestinal disordersMonotherapy Treatment With Eribulin7537
otherAlopeciaSkin and subcutaneous tissue disordersMonotherapy Treatment With Eribulin185318
otherAstheniaMusculoskeletal and connective tissue disordersMonotherapy Treatment With Eribulin7537
otherMusculoskeletal disorderMusculoskeletal and connective tissue disordersMonotherapy Treatment With Eribulin7537
otherBone painMusculoskeletal and connective tissue disordersMonotherapy Treatment With Eribulin5535

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMonotherapy Treatment With Eribulin2253
Total, other adverse eventsMonotherapy Treatment With Eribulin3953
Total, serious adverse eventsMonotherapy Treatment With Eribulin1153

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.

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/NCT02061085

GET https://conductscience.org/api/trials/v1/NCT02061085/events?page=2