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
Cite this record
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
On this page
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.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to Progression | Through study completion, up to 27 months | Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) |
| Secondary | Duration of Response | Through study completion, up to 27 months | Duration of response |
| Secondary | Clinical Benefit Rate | Through study completion, up to 27 months | |
| Secondary | Progression Free Survival | Through study completion, up to 27 months |
Source ClinicalTrials.gov
Outcomes4
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Time to Progression | Through study completion, up to 27 months | months | MEDIAN | |
| SECONDARY | Duration of Response | Through study completion, up to 27 months | months | MEDIAN | |
| SECONDARY | Clinical Benefit Rate | Through study completion, up to 27 months | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Progression Free Survival | Through study completion, up to 27 months | Months | MEDIAN |
Source ClinicalTrials.gov
Results by group4
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Time to Progression | Monotherapy Treatment With Eribulin | 4.1 | 95% Confidence Interval 3.2 to 6.6 | months | |
| Duration of Response | Monotherapy Treatment With Eribulin | 4.5 | Full Range 2.1 to 20.9 | months | |
| Clinical Benefit Rate | Monotherapy Treatment With Eribulin | 14 | Participants | ||
| Progression Free Survival | Monotherapy Treatment With Eribulin | 4.1 | 95% Confidence Interval 3.2 to 6.6 | Months |
Source ClinicalTrials.gov
Participant flow3
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Monotherapy Treatment With Eribulin | 53 | |
| Overall Study | COMPLETED | Monotherapy Treatment With Eribulin | 45 | |
| Overall Study | NOT COMPLETED | Monotherapy Treatment With Eribulin | 8 |
Source ClinicalTrials.gov
Adverse events27
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Neuropathy peripheral | Nervous system disorders | Monotherapy Treatment With Eribulin | 10 | 53 | 10 |
| other | Dry mouth | General disorders | Monotherapy Treatment With Eribulin | 4 | 53 | 4 |
| other | Nausea | Gastrointestinal disorders | Monotherapy Treatment With Eribulin | 14 | 53 | 14 |
| other | Constipation | Gastrointestinal disorders | Monotherapy Treatment With Eribulin | 10 | 53 | 10 |
| other | Anorexia and bulimia syndrome | Gastrointestinal disorders | Monotherapy Treatment With Eribulin | 10 | 53 | 10 |
| other | Abdominal pain | Gastrointestinal disorders | Monotherapy Treatment With Eribulin | 7 | 53 | 7 |
| other | Alopecia | Skin and subcutaneous tissue disorders | Monotherapy Treatment With Eribulin | 18 | 53 | 18 |
| other | Asthenia | Musculoskeletal and connective tissue disorders | Monotherapy Treatment With Eribulin | 7 | 53 | 7 |
| other | Musculoskeletal disorder | Musculoskeletal and connective tissue disorders | Monotherapy Treatment With Eribulin | 7 | 53 | 7 |
| other | Bone pain | Musculoskeletal and connective tissue disorders | Monotherapy Treatment With Eribulin | 5 | 53 | 5 |
1 to 10 of 27Source ClinicalTrials.gov
See all 27 adverse eventsAdverse event totals3
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Monotherapy Treatment With Eribulin | 22 | 53 |
| Total, other adverse events | Monotherapy Treatment With Eribulin | 39 | 53 |
| Total, serious adverse events | Monotherapy Treatment With Eribulin | 11 | 53 |
Source ClinicalTrials.gov
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.
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