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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05797493
Other study ID # 5061
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 4, 2022
Est. completion date June 2027

Study information

Verified date April 2023
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Emilio Bria, Prof.
Phone +39 0630156318
Email emilio.bria@policlinicogemelli.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The scope of the PICASSO project is to apply an innovative patient-based pan-omic approach to immune-assays, that will include multi-omics tumour characterization (genome, proteome, transcriptome), blood immune-cells and cytokine profiling, serological screening for paraneoplastic autoantibodies, clinical and metabolic measurements. The PICASSO project is aimed to validate in real world population the predictive role of SCLC transcriptomic classification (particularly, I-SCLC subtype) and to explore correlations with dynamic changes in peripheral blood immunity. Additionally, investigators expected to validate the predictive/prognostic role of emerging new variables, including metabolic-induced meta-inflammation alterations and subclinical auto-immunity.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date June 2027
Est. primary completion date June 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. histologically- or cytologically-documented extensive-stage SCLC 2. to have received upfront treatment with Cisplatin/Carboplatin, etoposide and anti PD1/PD-L1 inhibitors 3. No evidence of brain metastases at diagnosis 4. ECOG PS 0-2 5. adult patients (aged = 18 years) at diagnosis; 6. signing of informed consent approved by the local Ethic Committee Exclusion Criteria: - none

Study Design


Intervention

Drug:
Atezolizumab
Upfront chemo-immunotherapy

Locations

Country Name City State
Italy Fondazione Policlinico Gemelli IRCCS Rome

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary PFS Time from treatment start until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months Up to 60 months
Primary OS Time from treatment start to the date of death from any cause, assessed up to 60 months Up to 60 months
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