A Non Interventional Study With Doce Onkovis (Docetaxel) Utilized for the Treatment of Cancer

The main purpose of this observational study with Docetaxel is to determine the number of treatment cycles and the quantity of Doce onkovis needed therefore under the special circumstance of ambulant chemotherapy.

onkovis aims an economical utilization of the chemotherapeutics.The provision with adapted packaging sizes as to decrease the excess quantity to be discarded follows also this objective.

Secondary objectives are the evaluation of the safety and tolerability of Doce onkovis. To this purpose data regarding co medications and adverse events are also collected.

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Key information

Conditions

Carcinoma Breast Diseases Breast Neoplasms Bronchial Neoplasms Carcinoma, Bronchogenic Carcinoma, Non-Small-Cell Lung Lung Diseases Lung Neoplasms Neoplasms Neoplasms by Histologic Type Neoplasms by Site Neoplasms, Glandular and Epithelial Respiratory Tract Diseases Respiratory Tract Neoplasms Skin Diseases Skin and Connective Tissue Diseases Thoracic Neoplasms

Sex eligibility

All sexes

Study type

Observational

Primary location

Practice, Berlin, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Indication for Docetaxel according to the SmPC and treating physician

Exclusion criteria

according to the Docetaxel SmPC

Treatment and study plan

Primary outcomes

the quantity of Doce onkovis needed pro treatment cycle

Time frame: the time the participants will be followed depends on the number of treatment cycles; that means the time frame may extend up to 24 weeks (8 cycles).

Determine the quantity of Doce onkovis needed pro treatment cycle

Secondary outcomes

adverse events during and after treatment

Time frame: up to 24 weeks (8 cycles)

The number and kind of adverse events during and after the intra-venous application of Docetaxel will be assessed and documented.

Sponsors and collaborators

Lead sponsor

Onkovis GmbH

Industry

Collaborators

AKP Freiburg GmbH

Registry information

Official study title

Open, Multicenter Observational Study of Docetaxel Utilized in Mono- or Combination Therapy for Treatment of Breast Cancer, NSCLC, Prostate Carcinoma, Adenocarcinoma of Stomach and Advanced Squamous Cell Carcinoma of Head/Neck Region.

Important dates

Study start: 2012
Primary completion: 2015
Study completion: 2015
First posted: Jun 7, 2012
Registry last updated: Jun 4, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed