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Real-World Study of the BV-ICE Regimen in Relapsed/Refractory Classical Hodgkin Lymphoma

Real-World Study of the BV-ICE Regimen in Relapsed/Refractory Classical Hodgkin Lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127153
Enrollment
Unknown
Registered
2026-06-25
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Relapsed/refractory classical Hodgkin lymphoma

Interventions

PR before BV-ICE
non-PR before BV-ICE:None

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.histopathologically and immunohistochemically confirmed classical Hodgkin lymphoma (cHL); 2.relapsed or refractory after first-line standard therapy; 3.age >=16 years; 4.expected survival >= 3 months; 5.adequate organ function;

Exclusion criteria

Exclusion criteria: 1.patients with other concomitant malignancies; 2.patients with severe cardiac, hepatic, renal, pulmonary, vascular, or endocrine diseases; 3.patients with known hypersensitivity to BV or any other drugs included in the regimen; 4.pregnant or lactating women; 5.patients deemed unsuitable for participation in this study by the investigators;

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival (PFS);

Secondary

MeasureTime frame
Disease Control Rate (DCR);Adverse Events (AEs);Complete Response Rate (CRR);Event-Free Survival (EFS);Objective Response Rate (ORR);Duration of Response(DOR);

Countries

China

Contacts

Public ContactMi Jianqing

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

mjq10597@rjh.com.cn+86 21 64370045

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026