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OpenTrials
Completed

NCT Number: NCT02517281

Prospective Clinical and Biologic Study of Secondary Cutaneous Effects in Targeted Cancer Therapies

The aim of the study is to do a descriptive analysis of the cutaneous toxicity observed in patients treated using targeted therapies in order to have a better understanding of the skin pathophysiology.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gustave Roussy Cancer Campus Grand Paris

Villejuif, Val de Marne, 94805, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with cancer beginning a targeted therapy
  • Patients able to follow the protocol
  • Age >/= 18 years old
  • Signed inform consent

Exclusion criteria

  • Patient unable to follow the protocol, having a non cooperative behavior or unable to come to follow up visits or unable to complete the study
  • Pregnant or breastfeeding woman

Treatment and study plan

Biopsy

Procedure

Primary outcomes

  1. Number of clinical secondary effects bind to targeted therapies

    Time frame: Every 28 days up to 5 years

    Dermatological exam including questionnaire, clinical examination and photographies

Sponsors and collaborators

Lead sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Other

Registry information

Acronym: SKINTARGET

Important dates

Study start
2011
Primary completion
2022
Study completion
2022
First posted
Aug 7, 2015
Registry last updated
Mar 20, 2026

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.