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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05287464
Other study ID # ARON-1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 10, 2022
Est. completion date December 31, 2024

Study information

Verified date October 2023
Source Hospital of Macerata
Contact Matteo Santoni, MD, PhD
Phone +3907332572960
Email mattymo@alice.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The ARON-1 Study is designed as an International Multicentric Retrospective Study to collect global experiences with the use of immuno-combinations in patients with metastatic RCC. Two Supplementary Studies (ARON-1α and ARON-1β) have been designed. The ARON-1α Supplementary Study has been designed to investigate for the presence of genomic signatures from tumor samples of patients treated with first-line immuno-combinations for advanced RCC. The ARON-1β Supplementary Study has been designed to charaterize the immune cell populations and assess their relationship with the clinical outcome of mRCC patients treated with first-line immuno-combinations


Recruitment information / eligibility

Status Recruiting
Enrollment 1220
Est. completion date December 31, 2024
Est. primary completion date June 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients aged >18y - Cytological or Histologically confirmed diagnosis of clear cell or non-clear cell RCC - Histologically or radiologically confirmed diagnosis of metastatic disease - First-line treatment with nivolumab plus ipilimumab or nivolumab plus cabozantinib or pembrolizumab plus axitinib or pembrolizumab plus lenvatinib or avelumab plus axitinib or atezolizumab plus bevacizumab Exclusion Criteria: - Patients without histologically confirmed diagnosis of RCC - Patients without histologically or radiologically confirmed metastatic disease - Patients treated with immuno-combinations not included in the list reported in the Inclusion Criteria Section

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
pembrolizumab plus axitinib
collect global experiences with the use of immuno-combinations in patients with metastatic RCC

Locations

Country Name City State
Italy Ospedale di Macerata, UOC Oncologia Macerata

Sponsors (1)

Lead Sponsor Collaborator
Hospital of Macerata

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression-Free Survival (PFS) March 31th, 2022
Primary Overall Survival (OS) March 31th, 2022
Primary Overall Response Rate (ORR) March 31th, 2022
Secondary Efficacy of immuno-combination in the elderly populaton Data on tumor assessment and response to therapy on elderly populaton will be statistically analyzed May 31th, 2022
Secondary Efficacy of immuno-combinations in patients with different metastatic sites (i.e. bone and brain metastases) Data on tumor assessment and response to therapy will be statistically analyzed May 31th, 2022
Secondary Prognostic role of smoking attitude and obesity in RCC patients treated with different immuno-combinations Statistical analysis of prognostic role of smoking attitude and obesity in treated RCC patients May 31th, 2022
Secondary Efficacy of different immuno-combinations in patients with non-clear RCC Data on tumor assessment and response to therapy in non-clear RCC will be statistically analyzed September 30th, 2022
See also
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Completed NCT01514448 - Safety and Efficacy of Everolimus in Metastatic Renal Cell Carcinoma After Failure of First Line Therapy With Sunitinib or Pazopanib Phase 4
Completed NCT01390519 - A Norwegian Observational Trial Evaluating the Treatment of Advanced Renal Cell Cancer Patients Under Treatment of Afinitor N/A