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Active, Not Recruiting

NCT Number: NCT05215470

CLARA: Somatic and Germline Mechanisms That Impact Renal Cancer Immunotherapy

The study is studying the joint contribution and interactions of germline variants and somatic mutations and their impact on Renal Cell Carcinoma (RCC) development and treatment (immunotherapy).

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hospital das Clínicas da Faculdade de Medicina de Ribeirao Preto - USP

Ribeirão Preto, São Paulo, 14040-900, Brazil

About this study

One hundred newly diagnosticated stage IV RCC patients will be recruited in the Ribeirao Preto Medical School.

Patients will be treated with immune checkpoint inhibitors (ICI) combination: nivolumab (3 mg/kg of body weight) plus ipilimumab (1 mg/kg) intravenously every three weeks for four doses, followed by nivolumab 480mg every four weeks, until progression, toxicity or complete two years of treatment.

Patients will be followed up for the clinical outcome (progression-free survival, best response, and overall survival).

Fresh-frozen primary tumor tissue will be collected for somatic genomic characterization.

Blood DNA will be genotyped for the identification of common germline variation, as well as ancestry determination.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Renal cell carcinoma patient: histological confirmed clear cell tumor;
  • First-line metastatic treatment;
  • Stage IV with at least one measured lesion;
  • Fresh-frozen primary tumor tissue available;
  • No previous immunotherapy or tyrosine kinase inhibitor treatment;
  • All International Metastatic RCC Database Consortium (IMDC) Risk Score;
  • Karnofsky Performance Scale (KPS) >=70;
  • >=18 years old.

Exclusion criteria

  • History of a known or suspected autoimmune disease;
  • Any condition requiring systemic treatment with corticosteroids;
  • Creatinine clearance < 40mL/min;
  • Alanine aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) > 5 x ULN;
  • Pregnant women.

Treatment and study plan

Nivolumab

Drug

Nivolumab is called an anti-PD-1 (Programmed Cell Death Ligand 1) or a checkpoint inhibitor and is an antibody (a type of human protein) designed to allow the body's own immune system to destroy tumors

Other names: Opdivo

Ipilimumab

Drug

Ipilimumab is called an anti-CTLA-4 (cytotoxic T-lymphocyte-associated protein 4) and is a type of antibody that works to prevent the body's immune system from stopping to fight a specific cancer

Other names: Yervoy

Primary outcomes

  1. Overall Survival

    Time frame: 3 years

  2. Progression-free survival

    Time frame: 2 years

Secondary outcomes

  1. Overall Response Rate

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Hospital das Clínicas de Ribeirão Preto

Other

Collaborators

  • Bristol-Myers Squibb
  • Fundação de Amparo à Pesquisa do Estado de São Paulo

Registry information

Official study title

CLARA: Characterization of Somatic and Germline Mechanisms That Impact the Immunotherapy Treatment and Prognosis of Patients With Renal Cancer

Important dates

Study start
2022
Primary completion
2024
Study completion
2026
First posted
Jan 31, 2022
Registry last updated
Jul 3, 2024

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.

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