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Clinical Trials/CTIS2023-504994-19-00
CTIS2023-504994-19-00
Active, not recruiting
Phase 1

A Phase II Study Evaluating the Safety and Efficacy of Glofitamab in Combination with Rituximab (R) Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) in Circulating Tumor (ct)DNA High-Risk Patients with Untreated Diffuse Large B-Cell Lymphoma - GO43075

F. Hoffmann-La Roche AG0 sites40 target enrollmentApril 16, 2024

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
F. Hoffmann-La Roche AG
Enrollment
40
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 16, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Previously untreated patients with cluster of differential (CD20\)\-positive DLBCL, including diagnoses by the 2016 World Health Organization (WHO) classification of lymphoid neoplasms, International Prognostic Index (IPI): 1\-5, Life expectancy of \>\=6 months, Adequate biomarker blood samples prior to initiation of R\-CHOP on Day 1 of Cycle 1 and on Day 1 of Cycle 2 submitted for screening for determination of ctDNA status, At least one bi\-dimensionally fluorodeoxyglucose (FDG)\-avid measurable lymphoma lesion on positron emission tomography/computed tomography (PET/CT) scan, Left ventricular ejection fraction (LVEF) \>\=50%, as determined on cardiac multiple\-gated acquisition (MUGA) scan or cardiac echocardiogram (ECHO)

Exclusion Criteria

  • Contraindication to any of the individual components of R\-CHOP, including prior receipt of anthracyclines, history of severe allergic or anaphylactic reactions to murine monoclonal antibodies, or known sensitivity or allergy to murine products, Prior treatment for indolent lymphoma, Prior solid organ or allogeneic stem cell transplant, Positive SARS\-CoV\-2 test within 7 days prior to enrollment. Rapid antigen test result is also acceptable, Prior therapy for DLBCL and high\-grade B\-cell lymphoma (HGBCL) with the exception of palliative, short\-term treatment with corticosteroids, Pregnant or breastfeeding, or intending to become pregnant during the study or within 12 months after the final dose of R\-CHOP, 3 months after the final dose of tocilizumab (if applicable), or 2 months after the final dose of glofitamab

Outcomes

Primary Outcomes

Not specified

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