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Efficacy and Safety of Glofitamab in the Real-World Treatment of Patients With Primary Refractory or Early Relapsed Diffuse Large B-Cell Lymphoma

Efficacy and Safety of Glofitamab in the Real-World Treatment of Patients With Primary Refractory or Early Relapsed Diffuse Large B-Cell Lymphoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122028
Enrollment
Unknown
Registered
2026-04-08
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Primary refractory and early relapsed diffuse large B-cell lymphoma (PR/ER DLBCL)

Interventions

Glofitamab Treatment Group:NA

Sponsors

Henan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years at the initiation of treatment; 2. Diagnosis of diffuse large B-cell lymphoma (DLBCL); 3. Meeting the definition of primary refractory or early relapsed disease, defined as failure to achieve complete remission (CR) after four cycles of first-line induction therapy, or radiographically confirmed relapse within 12 months after achieving CR at the completion of induction therapy; 4. Patients who plan to initiate or have recently initiated treatment with glofitamab, either as monotherapy or in combination, after study initiation.

Exclusion criteria

Exclusion criteria: 1. Patients who are currently participating in or plan to participate in any interventional clinical trial; 2. Patients who are deemed by the investigator to be unsuitable for participation in this study for any other reason.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate (ORR);

Secondary

MeasureTime frame
Adverse Events (AEs);All adverse events will be assessed and graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0, including: All adverse events (AEs);Progression-Free Survival (PFS);Overall Survival (OS);Disease Control Rate (DCR);Minimal Residual Disease (MRD);Complete Response Rate (CR Rate);

Countries

China

Contacts

Public ContactKeshu Zhou

Henan Cancer Hospital

drzhouks77@163.com+86 13674902391

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026