Evolocumab + Nivolumab for Kidney Cancer

EJ
Overseen ByEric Jonasch, MD
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a combination of two drugs: evolocumab (Repatha, a cholesterol-lowering medication) and nivolumab (Opdivo, an immunotherapy drug). The aim is to determine if they can control kidney cancer that has spread and does not respond to standard treatments. Researchers also seek to ensure the safety of this drug duo for participants. This trial suits individuals with kidney cancer that includes a clear-cell component, who have tried other treatments without success, and have no recent side effects from cancer treatment. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.

Do I have to stop taking my current medications for this trial?

The trial protocol does not specify if you must stop taking your current medications. However, you cannot receive any other systemic therapy for kidney cancer while participating in this trial. If you are on chemotherapy, immunotherapy, or other experimental cancer therapy, you must stop at least 2 weeks before starting the study treatment.

Will I have to stop taking my current medications?

The trial does not specify if you need to stop taking your current medications, but you cannot be on any other systemic therapy for kidney cancer while participating. If you are on chemotherapy, immunotherapy, or other experimental cancer therapy, you must stop at least 2 weeks before starting the trial.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research shows that both evolocumab and nivolumab have been tested in people, each with its own safety profile. Evolocumab is usually well-tolerated and is already approved to lower cholesterol, indicating a proven safety record. Nivolumab treats various cancers, including kidney cancer. Past studies have linked nivolumab to serious side effects like pneumonia and trouble swallowing, but these occur in only a small number of patients.

The combination of evolocumab and nivolumab is still under study specifically for kidney cancer. However, existing information on each drug alone offers some reassurance. This trial is in Phase 2, focusing on the safety of this combination for patients, and researchers have already collected initial safety data from earlier phases.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about using Evolocumab combined with Nivolumab for kidney cancer because this duo offers a novel approach. Unlike traditional treatments like surgery, targeted therapies, and other immunotherapies, this combination leverages different mechanisms. Evolocumab is a monoclonal antibody that targets PCSK9, primarily used to lower cholesterol, but here it may enhance immune response. Nivolumab, another monoclonal antibody, blocks the PD-1 pathway, helping the immune system attack cancer cells more effectively. Together, they could offer a new way to bolster the body's own defenses against cancer, potentially leading to improved outcomes for patients.

What evidence suggests that evolocumab and nivolumab might be effective for kidney cancer?

Research has shown that nivolumab, a type of immunotherapy, extends survival in people with advanced kidney cancer compared to other treatments. Patients taking nivolumab lived longer than those taking everolimus, another cancer drug. In this trial, participants will receive a combination of evolocumab and nivolumab. Evolocumab, typically used to lower cholesterol, is under study for its potential to enhance the immune system's ability to fight cancer. The combination of evolocumab and nivolumab aims to strengthen the body's defense against kidney cancer. Early studies suggest that this combination could improve treatment outcomes for people with metastatic renal cell carcinoma, a form of kidney cancer that has spread.12346

Who Is on the Research Team?

Eric Jonasch | MD Anderson Cancer Center

Eric Jonasch, MD

Principal Investigator

M.D. Anderson Cancer Center

Are You a Good Fit for This Trial?

This trial is for patients with metastatic renal cell carcinoma, a type of kidney cancer that has spread and doesn't respond to treatment. Participants should meet specific health criteria set by the researchers but these aren't detailed here.

Inclusion Criteria

Signed and dated IRB/IEC approved written informed consent form
My organs and bone marrow are working well.
My hepatitis B virus is undetectable with treatment.
See 8 more

Exclusion Criteria

I have recovered from cancer treatment side effects, except for hair loss or hormone issues.
I don't have any health issues that would interfere with the treatment.
Known hypersensitivity to study drugs or excipients
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive evolocumab and nivolumab on Day 1 of each cycle (every 4 weeks). Evolocumab is given as an injection under the skin, and nivolumab is given by vein over about 60 minutes.

12 months
1 visit per cycle (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Evolocumab
  • Nivolumab
Trial Overview The study tests whether combining two drugs, Evolocumab and Nivolumab, can manage advanced kidney cancer effectively. It also examines the safety profile of this drug combination in treating the disease.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Evolocumab + NivolumabExperimental Treatment2 Interventions

Evolocumab is already approved in United States, European Union for the following indications:

🇺🇸
Approved in United States as Repatha for:
🇪🇺
Approved in European Union as Repatha for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

M.D. Anderson Cancer Center

Lead Sponsor

Trials
3,107
Recruited
1,813,000+

Bristol-Myers Squibb

Industry Sponsor

Trials
2,731
Recruited
4,127,000+
Headquarters
New York City, USA
Known For
Oncology & Cardiovascular
Top Products
Eliquis, Opdivo, Revlimid, Orencia
Christopher Boerner profile image

Christopher Boerner

Bristol-Myers Squibb

Chief Executive Officer since 2023

PhD in Business Administration from the Haas School of Business, University of California, Berkeley; BA in Economics and History from Washington University in St. Louis

Deepak L. Bhatt profile image

Deepak L. Bhatt

Bristol-Myers Squibb

Chief Medical Officer since 2024

MD from Yale University; MSc in Clinical Epidemiology from the University of Pennsylvania

Cancer Prevention Research Institute of Texas

Collaborator

Trials
55
Recruited
98,900+

United States Department of Defense

Collaborator

Trials
940
Recruited
339,000+

Published Research Related to This Trial

The combination of cabozantinib (a tyrosine kinase inhibitor) and nivolumab (an immune checkpoint inhibitor) significantly improved progression-free survival, overall survival, and objective response rates in patients with untreated advanced renal cell carcinoma compared to sunitinib, supporting its approval as a first-line therapy.
While the safety profile of the combination treatment is generally manageable, it requires careful monitoring and management of overlapping adverse events, such as diarrhea and hepatotoxicity, to maintain patient tolerability and treatment effectiveness.
Management of adverse events associated with cabozantinib plus nivolumab in renal cell carcinoma: A review.McGregor, B., Mortazavi, A., Cordes, L., et al.[2023]
Nivolumab, an anti-PD-1 antibody, shows promising effects in the treatment of advanced renal cancer, indicating its potential as an effective immunotherapy option.
The manuscript highlights the role of nivolumab in harnessing the immune system to target and combat renal cancer, suggesting a new avenue for treatment in this challenging disease.
[Nivolumab (Anti-PD-1 antibody; ONO-4538/BMS-936558) in renal cancer].Ozono, S.[2018]
In a phase 3 trial involving 1096 patients with untreated advanced renal-cell carcinoma, nivolumab plus ipilimumab significantly improved overall survival rates (75% at 18 months) compared to sunitinib (60% at 18 months), indicating a more effective treatment option for patients with intermediate or poor prognostic risk.
The objective response rate was also higher with nivolumab plus ipilimumab (42%) compared to sunitinib (27%), although both treatments had a high incidence of treatment-related adverse events, with nivolumab plus ipilimumab showing a slightly lower rate of severe (grade 3 or 4) events (46% vs. 63%).
Nivolumab plus Ipilimumab versus Sunitinib in Advanced Renal-Cell Carcinoma.Motzer, RJ., Tannir, NM., McDermott, DF., et al.[2022]

Citations

A phase II study bolstering outcomes by optimizing ...A phase II study bolstering outcomes by optimizing immunotherapy strategies with evolocumab and nivolumab in patients with metastatic renal cell carcinoma ( ...
ASCO GU 2025: A Phase II Study Bolstering Outcomes ...Dr. Tian Zhang presented the ongoing BOOST-RCC phase II trial of evolocumab plus nivolumab in patients with metastatic renal cell carcinoma (mRCC).
Novel Immunotherapy Trials May Drive Progress in Kidney ...Various kidney cancer trials have combined agents such as A2a receptor inhibitors with immunotherapy backbones to potentially improve treatment outcomes.
Evolocumab + Nivolumab for Kidney CancerResearch shows that Nivolumab, when used for advanced kidney cancer, improved survival rates compared to another drug, everolimus, with patients living a median ...
Efficacy Data for Renal Cell Carcinoma (RCC) - OpdivoIn patients receiving OPDIVO 3 mg/kg with YERVOY 1 mg/kg every 3 weeks, immune-mediated nephritis with renal dysfunction occurred in 4.1% (27/666) of patients, ...
Safety Profile for Renal Cell Carcinoma (RCC) - OpdivoThe most frequent serious adverse reactions reported in ≥2% of patients who received OPDIVO with chemotherapy were pneumonia (11%), dysphagia (7%), esophageal ...
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