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Spots Global Cancer Trial Database for Ibrutinib Combination Therapy in Transplant Ineligible Individuals With Newly Diagnosed Primary CNS Lymphoma

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Ibrutinib Combination Therapy in Transplant Ineligible Individuals With Newly Diagnosed Primary CNS Lymphoma

Official Title: A Phase 2 Study of Ibrutinib Combination Therapy in Transplant Ineligible Individuals With Newly Diagnosed Primary Central Nervous System Lymphoma

Study ID: NCT05998642

Study Description

Brief Summary: This study is being done to answer the following question: Can the addition of a new drug to the usual treatment lower the chance of primary central nervous system lymphoma growing or spreading? This study is being done to find out if this approach is better or worse than the usual approach for this type of cancer. The usual approach is defined as the care most people get for Primary Central Nervous System Lymphoma (PCNSL).

Detailed Description: If a patient decides to take part in this study, the patient will get 3 months of treatment with methotrexate and ibrutinib as well as rituximab (if rituximab is given for PCNSL in the applicable province). This will be followed by treatment with ibrutinib alone for up to 2 years of total treatment time. After finishing study treatment, and even if patients stop treatment early, the study doctor will continue to follow the patient's condition for the rest of their life or until all study results are known (in approximately 6 years), watch for side effects and keep track of the patient's health. If there are any side effects that may be related to ibrutinib, the patient will be asked to come back to the clinic every 3 months until side effects improve. If there are no side effects from ibrutinib the patient will be asked to come back to clinic every 6 months until cancer worsens, and then every 6 months may be contacted by phone.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

BCCA - Vancouver Cancer Centre, Vancouver, British Columbia, Canada

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada

University Health Network, Toronto, Ontario, Canada

CHU de Quebec-Hopital l'Enfant-Jesus (HEJ), Quebec City, Quebec, Canada

Contact Details

Name: Jean-Francois Larouche

Affiliation: CHU de Quebec-Hopital l'Enfant-Jesus (HEJ), Quebec City, QC Canada

Role: STUDY_CHAIR

Name: Anca Prica

Affiliation: University Health Network-Princess Margaret Hospital, Toronto, ON Canada

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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