Study of Mosunetuzumab and Polatuzumab Vedotin Combination Treatment in Patients with B-Cell Non-Hodgkin Lymphoma

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What is this study about?

This clinical trial studies the combination of two medications – mosunetuzumab and polatuzumab vedotin – in patients with B-cell non-Hodgkin lymphoma. This type of lymphoma is a cancer that starts in white blood cells called B cells. The study includes patients whose disease has returned or did not respond to previous treatments.

The medications being tested are both types of targeted therapies. Mosunetuzumab is a specially designed antibody that helps the immune system recognize and attack cancer cells. Polatuzumab vedotin is a medication that combines an antibody with a substance that kills cancer cells. The study will test these medications given together through intravenous infusion or as an injection under the skin.

The study will check if this combination of medications is safe to use and how well it works in treating the lymphoma. Researchers will monitor patients for side effects and measure if the cancer responds to the treatment. The study will also look at how long any improvements last and how the medications move through the body. Additional medications may be given to help manage side effects, including prednisone, dexamethasone, paracetamol, and other supportive care medicines.

1 Initial Treatment Phase

You will receive a combination of two main medications through intravenous infusion (delivered directly into your vein):

Mosunetuzumab

Polatuzumab vedotin

Before the main treatment, you will receive preparatory medications to help manage potential reactions:

Paracetamol (oral tablet)

Diphenhydramine (antihistamine medication through infusion)

Methylprednisolone (steroid medication through infusion)

2 Monitoring Phase

Regular assessments will track your response to treatment including:

– Blood tests to check laboratory values

– Vital signs monitoring

– Measurement of tumor response using imaging scans

3 Additional Support Medications

You may receive additional medications as needed:

Rituximab (through infusion)

Tocilizumab (through infusion)

Allopurinol (oral medication)

These medications help manage side effects and support your treatment

4 Follow-up Assessments

Regular evaluation of your condition will continue to track:

– How well the treatment is working

– Any side effects that may occur

– Your overall health status

The study is expected to continue until July 2025

Who Can Join the Study?

  • Must be 18 years or older when signing the consent form
  • Must have confirmed relapsed or refractory (returning or not responding to treatment) follicular lymphoma (FL), diffuse large B-cell lymphoma (DLBCL), or mantle cell lymphoma (MCL)
  • For patients with DLBCL or FL: Must have received at least one previous treatment that included therapy targeting CD20 (a protein found on certain blood cells)
  • For patients with MCL: Must have received at least two previous treatments including:
    – Treatment targeting CD20
    – A BTK inhibitor (medication that blocks a specific protein)
    – Either anthracycline or bendamustine (types of chemotherapy drugs)
  • Must have an ECOG Performance Status of 0, 1, or 2 (a measure of daily living abilities, where 0 means fully active and 2 means able to do light activities)
  • Must have measurable disease with at least one of these:
    – A lymph node larger than 1.5 centimeters
    – A tumor outside lymph nodes larger than 1.0 centimeter

Who Cannot Join the Study?

  • History of severe allergic reactions or anaphylaxis (serious allergic reaction)
  • Active infections requiring treatment, including hepatitis B, hepatitis C, or HIV
  • Presence of active central nervous system lymphoma (cancer affecting brain or spinal cord)
  • Prior treatment with CAR T-cell therapy (a type of cell-based cancer treatment) within 3 months before starting the study
  • Significant heart problems, including heart failure or uncontrolled heart rhythm disorders
  • Severe liver problems or abnormal liver function tests
  • Severe kidney problems or abnormal kidney function
  • History of other cancers within the past 2 years (except for successfully treated skin cancers or early-stage cancers)
  • Pregnancy or breastfeeding
  • Participation in another clinical trial within 28 days before starting this study
  • Inability to comply with study procedures or follow-up visits
  • Major surgery within 4 weeks before starting the study
  • Serious medical conditions that could interfere with study participation

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

No sites found in this category

Other Sites

Site Name City Country Status
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital San Pedro De Alcantara Caceres Spain
Hospital Universitario Infanta Leonor Madrid Spain
Vrije Universiteit Brussel Jette Belgium
Clinique Saint-Pierre Ottignies (CSPO) Ottignies Belgium
Iablppun Cxqmmq Dttnptkrywxycpcad L'hospitalet De Llobregat Spain
Hrdukqr Jxoykaww Haine-Saint-Paul Belgium

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
29.03.2021
Spain Spain
Not recruiting
29.03.2021

Trial locations

Mosunetuzumab is a medication designed to target and treat B-cell lymphomas. It works by helping the body’s immune system recognize and attack cancer cells, specifically in patients with non-Hodgkin lymphoma. This medication can be given either through an intravenous (IV) infusion directly into the vein or as a subcutaneous (under the skin) injection.

Polatuzumab vedotin is an antibody-drug conjugate that specifically targets B-cells in non-Hodgkin lymphoma. It works by delivering a cancer-killing substance directly to cancer cells. This targeted approach helps to destroy cancer cells while limiting damage to healthy cells. The medication is given through an intravenous (IV) infusion.

These medications are being studied in combination to treat patients with different types of B-cell non-Hodgkin lymphoma, including diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL), particularly in cases where previous treatments have not worked or the disease has returned.

B-cell non-Hodgkin lymphoma – A type of blood cancer that develops in the lymphatic system from B-cells, which are white blood cells that help fight infections. The disease begins when healthy B-cells transform into abnormal cells that grow and divide uncontrollably. These abnormal cells can develop in any part of the body where lymph tissue is found, including lymph nodes, spleen, and bone marrow. The condition can be either aggressive (fast-growing) or indolent (slow-growing). The disease can cause enlarged lymph nodes, fever, night sweats, and unexplained weight loss.

Diffuse Large B-cell Lymphoma (DLBCL) – An aggressive form of B-cell non-Hodgkin lymphoma that affects the B-cells in the lymphatic system. The disease is characterized by the rapid growth of abnormally large B-cells that spread throughout lymph nodes and can affect other organs. It typically presents as quickly growing masses in lymph node areas.

Follicular Lymphoma (FL) – A slow-growing type of B-cell non-Hodgkin lymphoma that develops when B-cells become abnormal and collect in lymph nodes. The disease is characterized by the circular arrangement of abnormal B-cells in the lymph nodes, forming follicles. It typically progresses slowly and can affect multiple lymph node sites.

Mantle Cell Lymphoma (MCL) – A rare type of B-cell non-Hodgkin lymphoma that starts in the outer edge of lymph nodes called the mantle zone. The disease develops when B-cells in the mantle zone become abnormal and multiply uncontrollably. It can spread to other parts of the body including the bone marrow, blood, and other organs.

Trial ID:
2023-506986-74-00
Protocol code:
GO40516
Trial Phase:
Human Pharmacology (Phase I) – Other

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