Nivolumab Combined With Ipilimumab Versus Sunitinib in Previously Untreated Advanced or Metastatic Renal Cell CarcinomaLast updated: April 09, 2018 STATUS: Closed to accrual (not accepting new patients) (per ClinicalTrials.gov/NCT02231749)
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WHOis the trial for? |
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WHATis the key question that this trial is attempting to answer? |
This phase-III study seeks to clarify whether the new immunotherapies are superior
to one of the standard therapies for kidney cancer.
This particular study investigates the combination of the immune-checkpoint inhibitors
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WHYpatients might want to participate? |
This clinical trial offers patients an opportunity to access a new therapy that may be effective for kidney cancer. This trial will further support the research in kidney cancer and potentially help other patients with kidney cancer. The trial might or might not have benefit in your individual case. For more about the importance and benefits of joining clinical trials, please click here. |
WHENwill the trial be open? |
The study is closed to accrual (not accepting new patients) – approx. 1070 patients worldwide are participating. |
WHEREis the trial available? |
The trial was available in 184 cancer centres worldwide in 28 countries.
For a complete list of trial locations, please download the following document: |
STUDYDESIGNWhat does the study look like? |
There will be 2 study arms (groups): all participating patients will be randomly divided (by a computer) in two groups. Please note that patients in both groups will receive an active medication. No patient receives a placebo. Patients in one group will be assigned nivolumab (OpdivoTM) in combination with ipilimumab (YervoyTM). Patients in the other group will be treated with sunitinib (SutentTM), which is an approved treatment for RCC.
1) The combination of nivolumab and ipilimumab is given intravenously every 3 weeks for 4 doses. 2) After that patients will receive nivolumab intravenously every 2 weeks until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the end of the study. 3) Sunitinib is taken by mouth once daily for 4 weeks then 2 weeks off, continuously until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends. |
HOWdo I get more information? |
Patient organisations supporting kidney cancer patients in your country may offer additional information about the trial, current recruitment status, and key contacts. Click here for a list of patient organisations serving kidney cancer patients. If there are no such organisations in your country, please email us for more information: This email address is being protected from spambots. You need JavaScript enabled to view it. |
CONNECTwith other patients on this trial |
If you want to connect with other patients considering or participating in this trial, you can find them here: List of organisations worldwide. |
SHAREyour experience |
You want to share your experience on this trial? Send us an e-mail to: This email address is being protected from spambots. You need JavaScript enabled to view it. Note that your experience would be helpful for other patients and patient organisations. |
RESULTSof the study |
No results are available at this time. Future results will be linked here. |