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OpenTrials
Completed

NCT Number: NCT03379012

Testosterone in Metastatic Renal Cell Carcinoma Patients

Purpose

To determine efficacy and safety of Testosterone in male patients with metastatic renal cell carcinoma and fatigue receiving targeted therapy or checkpoint inhibitors.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

A.I. Kryzhanovsky Krasnoyarsk Cancer Center, Krasnoyarsk, Russia

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About this study

Fatigue is a frequent symptom of metastatic renal cell carcinoma (RCC), and most common adverse event of targeted and immunotherapy.

In Phase 3 pivotal studies, 56% (9%, grade 3-4), 54% (11%, grade 3), 37% (10%, grade 3-4) and 20% (2%, grade 3) of patients had fatigue during the therapy of cabozantinib, sunitinib, axitinib or pazopanib, respectively. 59% (14%, grade 3) and 31% (5%, grade 3) of patients treated with lenvatinib/everolimus and everolimus had fatigue in registrational trials. Finally, 33% (2%, grade 3-4) of patients that received nivolumab had fatigue in CheckMate 025 study.

Testosterone may help to relieve fatigue associated with the use of tyrosine kinase, mTOR or checkpoint inhibitors. Additionally, testosterone could impact on poor prognostic factors of RCC (anemia, ECOG performance status, serum calcium). This will be first clinical trial which evaluates safety and efficacy of Testosterone in RCC patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically proven clear cell renal cell carcinoma;
  • CT-confirmed metastatic measurable disease;
  • First-line sunitinib or pazopanib treatment with fatigue;
  • Low level of testosterone;
  • Male, 18 years and older; 5. Normal PSA level

Exclusion criteria

  • Prostate and other cancers history
  • Hypothyroidism
  • History of serious cardiac arrhythmia, congestive heart failure, angina pectoris, or other severe cardiovascular disease (i.e., New York Heart Association class III or IV)

Treatment and study plan

Testosterone undecanoate and sunitinib or pazopanib

Drug

Testosterone undecanoate (Nebido®) 1,000 mg (4 ml) intramuscular deeply, once before targeted therapy (sunitinib 50 mg 4/2 or pazopanib 800 mg daily)

Primary outcomes

  1. Fatigue

    Time frame: 3 months

    Difference in mean change of Fatigue from baseline score with testosterone vs. without testosterone.

Secondary outcomes

  1. Safety and tolerability

    Time frame: 3 months

    Safety and tolerability of testosterone (CTCAE v.4.03)

  2. Quality of life

    Time frame: 3 months

    Health-related quality of life (NCCN-FACT FKSI-19 (Version 2)

  3. Overall rate of adverse events

    Time frame: 3 months

    Overall rate of adverse events related with TKI treatment (CTCAE v.4.03)

  4. Testosterone serum concentrations

    Time frame: 12 weeks

    Maximum and minimum total testosterone serum concentrations following dose administration at week 12

  5. Red blood cell count and Hemoglobin concentration

    Time frame: 12 weeks

    Change in Red blood cell count and Hemoglobin concentration following dose administration at week 12

  6. Serum calcium concentration

    Time frame: 12 weeks

    Change in serum calcium concentration following dose administration at week 12

  7. ECOG PS

    Time frame: 3 months

    ECOG Performance status

  8. Overall survival

    Time frame: 2 years

    Time from randomization to death

Sponsors and collaborators

Lead sponsor

Kidney Cancer Research Bureau

Other

Registry information

Official study title

Phase 2 Randomized Study of Efficacy and Safety of Testosterone in Metastatic Renal Cell Carcinoma Patients With Fatigue

Acronym: FARETES

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Dec 20, 2017
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.

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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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