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Clinical Trials in Switzerland / NCT04510766
Recruiting Observational

Tumor Molecular Profiling in Early Phase Clinical Trials

NCT04510766 · tracked via the Priya Life Science Switzerland tracker
Phase
Observational
Started
2020-10-01
Last updated
2025-11-18

Condition(s) studied

Advanced Solid TumorLymphoma

Study summary

Prospective, single centre, non-interventional exploratory research project that will be conducted on biological material and health-related personal data collected.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Male or female patients age at least 18 years. 2. Patients with histological diagnosis of advanced solid tumor or lymphoma who are potential candidates for early phase clinical trials. 3. Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1 4. Live expectancy of at least 6 months. 5. Availability of FFPE archival tumor tissue from previous surgery or diagnostic biopsy adequate for molecular analysis. 6. Ability to understand the patient information and study consent. Signed and dated written informed consent must be available before performing any study-related procedure. 7. Willing and able to comply with study procedures Exclusion Criteria: 1. Presence of any clinical (e.g. concomitant disease, clinically significant symptoms, or non-clinical (psychological or social) conditions that would not make the patient eligible for enrolment in an early phase clinical trial. 2. Any other active malignancy (other than the one for which the subject is being assessed for trial option) that is progressing or requiring active treatment with the exception of basal or squamous cell skin cancer, superficial bladder cancer, carcinoma in situ of any site.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Oncology Institute of Southern Switzerland Bellinzona Switzerland Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04510766 on ClinicalTrials.gov ↗ ← All trials in Switzerland