New hope for aggressive lymphoma: targeted combo trial launches
NCT ID NCT07511114
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a new drug combination (C Pola R-CHP+X) works better than the standard treatment (CR-CHOP) for people with a fast-growing type of lymphoma called double-expressor diffuse large B-cell lymphoma. About 156 adults aged 18-75 who have not been treated before will take part. The goal is to see if the new combo leads to more complete remissions and longer survival.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 156 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 1\. Histopathological diagnosis confirmed as diffuse large B-cell lymphoma, with CD20 positivity; * 2\. Simultaneous expression of MYC and BCL2, according to the WHO standard for immunohistochemistry: MYC ≥ 40%, BCL2 ≥ 50% * 3\. Age ≥ 18 years old and ≤ 75 years old; * 4\. ECOG performance status score of 0, 1, or 2; * 5\. International Prognostic Index (IPI) \> 1 * 6\. No history of malignant tumor; no concurrent occurrence of other tumors; * 7\. Patients with an expected lifespan of at least 6 months, as determined by the researcher; * 8\. The patient or their legal representative must provide written informed consent before undergoing any special examinations or procedures in the study. Exclusion Criteria: * 1\. Have previously received systemic or local treatments, including chemotherapy; * 2\. Have previously undergone autologous stem cell transplantation; * 3\. Previously had a history of other malignant tumors, excluding basal cell carcinoma and cervical carcinoma in situ; * 4\. Accompanied by uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, severe infectious diseases, etc; * 5\. Primary central nervous system lymphoma; * 6\. Left ventricular ejection fraction (LVEF) is less than or equal to 50%; * 7\. Laboratory test values during screening: (unless caused by lymphoma); A. Neutrophil count \<1.5\*10\^9/L; B. Platelet count \< 75 x 10\^9/L; C. ALT or AST is 2 times higher than the upper limit of normal, and AKP and bilirubin are 1.5 times higher than the upper limit of normal; D. Creatinine level is higher than 1.5 times the upper limit of normal; * 8\. Other concurrent and uncontrolled medical conditions that the researcher believes will affect the patient's participation in the study. * 9\. Patients with mental illness or other patients known or suspected to be unable to fully comply with the study protocol; * 10\. Pregnant or lactating women; * 11\. Individuals infected with HIV. * 12\. Patients with positive HBsAg test results must undergo HBV DNA testing and can only be enrolled after becoming negative. Additionally, if the HBsAg test result is negative but the HBcAb test result is positive (regardless of the HBsAb status), HBV DNA testing is also required. If the result is positive, treatment must be administered until becoming negative before enrollment;
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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No. 197 Ruijin 2nd Road, Huangpu District, Shanghai, Shanghai, Shanghai
Shanghai, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a new drug combo reach lymphoma hiding in the brain?
- Can a new drug combo boost remission in aggressive lymphoma?
- Can a Four-Pronged attack beat brain lymphoma?
- Can a new drug combo outsmart resistant lymphomas?
- Can a targeted drug boost standard chemo for aggressive lymphoma?
- Can a targeted drug combo outsmart an aggressive lymphoma?