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Spots Global Cancer Trial Database for Evaluation of Tolerance and Efficacy Retrospective Data of XOFIGO

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Trial Identification

Brief Title: Evaluation of Tolerance and Efficacy Retrospective Data of XOFIGO

Official Title: Evaluation of Tolerance and Efficacy Retrospective Data of XOFIGO Prescribed by AMM in Prostate Cancer

Study ID: NCT04516707

Interventions

clinical database

Study Description

Brief Summary: Since 13 November 2013, XOFIGO has been authorised on the European zone for the treatment of patients with prostate cancer, in the phase of resistance to castration, with symptomatic bone metastases. bone metastases frequently give rise to "bone events" that include spinal cord compressions and pathological fractures requiring surgery or external radiotherapy. Bone metastases are an important cause of death, disability, quality of life degradation and increase the cost of treatment. Xofigo is indicated in patients with bone metastases symptomatic of hormone-resistant prostate cancer and without known visceral metastases.

Detailed Description: Since 13 November 2013, XOFIGO has been authorised on the European zone for the treatment of patients with prostate cancer, in the phase of resistance to castration, with symptomatic bone metastases. Prostate cancer is the most common non-cutaneous cancer in men internationally, and more than 90% of patients with hormone-resistant prostate cancer will have bone metastases. They frequently give rise to "bone events" that include spinal cord compressions and pathological fractures requiring surgery or external radiotherapy. Bone metastases are an important cause of death, disability, quality of life degradation and increase the cost of treatment. There is therefore a need for bone-targeting therapeutic agents that provide a benefit in terms of survival. Xofigo is indicated in patients with bone metastases symptomatic of hormone-resistant prostate cancer and without known visceral metastases. This treatment appears to have fewer side effects than chemotherapy (and does not call into question subsequent chemotherapy) or that the currently available metabolic bone radiotherapy as well as better pain control and survival gain than the latter do not

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Icm Val D'Aurelle, Montpellier, Herault, France

ICO Bordeaux, Bordeaux, , France

UP Clermont Ferrand, Clermont-Ferrand, , France

Chu Grenoble, Grenoble, , France

IPC Marseille, Marseille, , France

CRLC de Nantes, Nantes, , France

APHP Hopital Cochin, Paris, , France

ONCOLOPE, Toulouse, , France

Contact Details

Name: Emmanuel DESHAYES, MD

Affiliation: ICM Val d'Aurelle

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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