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Clinical study of Fuzheng Jiedu prescription on immune escape of diffuse large B-cell lymphoma

Clinical study of Fuzheng Jiedu prescription on immune escape of diffuse large B-cell lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000828
Enrollment
Unknown
Registered
2024-12-15
Start date
2024-10-09
Completion date
Unknown
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diffuse large B-cell lymphoma

Interventions

Experimental group:Receive Fuzheng Jiedu prescription combined with standard treatment.
Control group:Receive only standard treatment.

Sponsors

Shanghai tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria Age: Adult patients 18 years and older. Diagnosis: Diffuse large B-cell lymphoma (DLBCL) was confirmed which met the WHO classification criteria. Stage: Any clinical stage (stage I-IV) that may include patients with initial treatment or relapse. Treatment history: May include patients who have not received treatment or patients who have received monotherapy. Physiological state: have good physiological state Karnofsky score =70. Informed consent: Be able to understand the purpose of the study and sign informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria Complicated diseases: There are serious cardiovascular liver kidney and other organ insufficiency or other major diseases. Other tumors: Patients who have had other malignancies recently (within the last 5 years). Allergy history: Patients with a history of allergy to the ingredients of the investigational drug. Immunosuppression: Patients who are receiving immunosuppressive treatment (such as long-term use of hormones or chemotherapy). Pregnancy or lactation: Female patients were pregnant nursing or planning to become pregnant during the study period. Participating in other studies: Patients currently participating in other clinical studies.(YNMT)·

Design outcomes

Primary

MeasureTime frame
Overall response rate;

Secondary

MeasureTime frame
Percentage of CD8+ T cell subsets;overall survival;The proportion of CD4+T cell subsets;progression free survival;

Countries

China

Contacts

Public ContactYidong Zhu

Shanghai tenth People's Hospital

zhuyidong0813@foxmail.com+86 137 0189 2865

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026