GALENOS 1 in Head and Neck, Lung, and Rectal Cancer Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFondazione del Piemonte per l'Oncologia

About this trial

GALENOS 1 is a prospective observational study designed to explore longitudinal changes in nutritional status and body composition in patients with head and neck squamous cell carcinoma, locally advanced rectal cancer, and lung cancer undergoing standard antineoplastic treatments. The study is the preparatory observational component of the FOR-GALE PREVENTION project, which aims to support the future development of a galenic immunonutrition dietary supplement intended to reduce adverse events and improve treatment compliance

Eligibility criteria

Qualifiers

Written informed consent provided before study procedures

Male or female participants aged 18 years or older

Histological or cytological documentation of head and neck squamous cell carcinoma, locally advanced rectal cancer, or lung cancer

Candidate for standard antineoplastic treatment according to clinical practice

Disqualifiers

Incomplete recovery from surgery before start of antineoplastic treatment

Other additional malignancies progressing or requiring active treatment within the previous 3 years, except localized basal cell carcinoma, localized squamous cell carcinoma of the skin, or cervical carcinoma in situ

Active infection requiring systemic antibiotic therapy Serious or unstable medical conditions, psychiatric disorders, or substance abuse that would interfere with study compliance

Receipt of any live vaccine within 30 days before planned start of study therapy

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

110 Participants
are grouped into 3 trial groups