Testosterone undecanoate and sunitinib or pazopanib
DrugTestosterone undecanoate (Nebido®) 1,000 mg (4 ml) intramuscular deeply, once before targeted therapy (sunitinib 50 mg 4/2 or pazopanib 800 mg daily)
NCT Number: NCT03379012
Purpose
To determine efficacy and safety of Testosterone in male patients with metastatic renal cell carcinoma and fatigue receiving targeted therapy or checkpoint inhibitors.
Looking for future studies?
Notify Me18 year and older
Male
Interventional
Phase 2
A.I. Kryzhanovsky Krasnoyarsk Cancer Center, Krasnoyarsk, Russia
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Testosterone undecanoate (Nebido®) 1,000 mg (4 ml) intramuscular deeply, once before targeted therapy (sunitinib 50 mg 4/2 or pazopanib 800 mg daily)
Time frame: 3 months
Difference in mean change of Fatigue from baseline score with testosterone vs. without testosterone.
Time frame: 3 months
Safety and tolerability of testosterone (CTCAE v.4.03)
Time frame: 3 months
Health-related quality of life (NCCN-FACT FKSI-19 (Version 2)
Time frame: 3 months
Overall rate of adverse events related with TKI treatment (CTCAE v.4.03)
Time frame: 12 weeks
Maximum and minimum total testosterone serum concentrations following dose administration at week 12
Time frame: 12 weeks
Change in Red blood cell count and Hemoglobin concentration following dose administration at week 12
Time frame: 12 weeks
Change in serum calcium concentration following dose administration at week 12
Time frame: 3 months
ECOG Performance status
Time frame: 2 years
Time from randomization to death
Kidney Cancer Research Bureau
Other
Phase 2 Randomized Study of Efficacy and Safety of Testosterone in Metastatic Renal Cell Carcinoma Patients With Fatigue
Acronym: FARETES
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.
Published trials that share one or more normalized conditions with this study.
NCT05858749
Adenocarcinoma, Carcinoma
New York, United States
View Trial DetailsNCT02231749
Adenocarcinoma, Advanced Renal Cell Carcinoma
Duarte, California, United States
View Trial DetailsNCT03075423
Adenocarcinoma, Carcinoma
Ghent, Belgium
View Trial DetailsNCT00930033
Adenocarcinoma, Carcinoma
Paris, France
View Trial Details