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Prospective non-interventional study of tumor-associated fatigue syndrome under Anthracyclintherapie - Face -E (pirubicin)

Prospective non-interventional study of tumor-associated fatigue syndrome under Anthracyclintherapie - Face -E (pirubicin) - FAce –E(pirubicin)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00007953
Enrollment
500
Registered
2015-08-25
Start date
2015-06-17
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Fatigue, tumor asscociated

Interventions

Group 1: Patients with histologically or cytologically confirmed various tumor entities for whom therapy with Epirubicin LIV Pharma is indicated according to the enclosed SmPC. The special warnings an

Sponsors

LIV Pharma GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Histologically or cytologically confirmed tumor diseases of the female breast or ovaries for which Epirubicin LIV Pharma is approved as a drug according to the specialist information - Age: older than 18 years - Epirubicin LIV Pharma is used in therapy. - A hand-dated and signed consent is available. - The therapy was selected independently of a possible study inclusion.

Exclusion criteria

Exclusion criteria: - Contraindications to the use of Epirubicin LIV Pharma according to the SmPC. - The current therapy was started more than 12 weeks ago. - The patient is participating in a clinical trial at the same time. - Pregnancy is present or the patient is breastfeeding.

Design outcomes

Primary

MeasureTime frame
Efficacy and Tolerability routine practice. Observational, non-interventional study.

Secondary

MeasureTime frame
Side effects which were not observed so far.

Countries

Germany

Contacts

Public ContactBurkard Heckelbacher

Datafaber GbR

heckelbacher@datafaber.de+49 8161 885 107

Outcome results

None listed

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