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Completed

NCT Number: NCT02700568

Axitinib in Metastatic Renal Cell Carcinoma Patients With Favorable Prognostic Factors

Aim of the FavorAx study is to evaluate preliminary efficacy and safety of Axitinib in metastatic renal cell carcinoma patients with favorable IMDC prognostic factors who had progressed on sunitinib or pazopanib in the first-line setting.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Demchenkova Marina Viktorovna, Irkutsk, Russia

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About this study

Axitinib is a tyrosine kinase inhibitor of vascular endothelial growth factor receptor, platelet-derived growth factor receptor-α, and c-kit. The trial of comparative effectiveness of axitinib versus sorafenib in advanced renal cell carcinoma (AXIS) was an international randomized Phase III study designed for registration purposes. This trial randomized 723 metastatic renal cell carcinoma patients with any prognostic features to axitinib or sorafenib in the second-line setting and demonstrated significant clinical benefit of axitinib.

Aim of present FavorAx study is to evaluate preliminary efficacy and safety of Axitinib in metastatic renal cell carcinoma patients with favorable IMDC prognostic factors who had progressed on sunitinib or pazopanib in the first-line setting.

Who can participate

Healthy volunteers accepted: No

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

Principle Inclusion Criteria:

  • Histologic confirmation of Renal cell carcinoma with a clear cell component
  • Patients must have measurable disease
  • Previous treatment with sunitinib or pazopanib
  • Favorable prognosis according to IMDC criteria
  • Must have available tumor tissue for submission
  • Subjects must also meet various laboratory parameters for inclusion
  • Patients must give written informed consent prior to initiation of therapy

Exclusion criteria

  • Any underlying medical condition, which in the opinion of the Investigator, will make the administration of study drug hazardous or obscure the interpretation of adverse events
  • Patients who have history of uncompensated diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that might affect the interpretation of the results of the study or render the subject at high risk from treatment complications.

Treatment and study plan

Axitinib

Drug

Initial dose of axitinib: 5 mg orally twice a day. Maintenance dose of axitinib: Increase or decrease dose based on individual safety and tolerability. Dose range of axitinib: 2 to 10 mg twice a day.

Other names: Inlyta

Primary outcomes

  1. Progression-free survival

    Time frame: 10 months

Secondary outcomes

  1. Objective response rate

    Time frame: 24 months

  2. Overall survival

    Time frame: 24 months

  3. Rate of treatment-related serious adverse events

    Time frame: 24 months

    Number of participants with treatment-related serious adverse events as assessed by CTCAE v4.0

Sponsors and collaborators

Lead sponsor

Kidney Cancer Research Bureau

Other

Registry information

Official study title

Evaluation of the Safety and Efficacy of Axitinib in Metastatic Renal Cell Carcinoma Patients With Favorable Prognostic Factors

Acronym: FavorAx

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Mar 7, 2016
Registry last updated
Oct 22, 2019

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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