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OncoSur Analysis of the Treatment in Third Line of ABC with Eribulin

?Multicenter study of a single arm to evaluate the safety of eribulin in 3rd line chemotherapy for patients with HER2-negative metastatic or locally advanced previously treated with anthracyclines and taxanes: Onsite Study" - ONCOSUR-2012-02

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2013-001416-30-ES
Enrollment
60
Registered
2013-09-05
Start date
2013-10-17
Completion date
Unknown
Last updated
2016-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Trade Name: HALAVEN 0,44 mg/ml solución inyectable Product Name: halaven Pharmaceutical Form: Solution for injection INN or Proposed INN: ERIBULIN CAS Number: 441045-17-6 Other descriptive name: ERIBU

Sponsors

Fundación Oncosur
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 60 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 60

Exclusion criteria

Exclusion criteria: -

Design outcomes

Primary

MeasureTime frame
Main Objective: -;Secondary Objective: -;Primary end point(s): -;Timepoint(s) of evaluation of this end point: -

Secondary

MeasureTime frame
Secondary end point(s): -;Timepoint(s) of evaluation of this end point: -

Countries

Spain

Contacts

Public ContactArancha Maciá

EXPERIOR

macia.arancha@experior.es0034902105 255129

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026