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A Study of Efficacy and Safety of Glofitamab in Combination With Salvage Therapy in a Real-world Setting in Chinese Adult Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma. (GLOFTST)

S

Soochow University

Status

Enrolling

Conditions

B-cell Non-Hodgkin Lymphoma

Treatments

Drug: Glofitamab

Study type

Observational

Funder types

Other

Identifiers

NCT06497452
GLOFTST

Details and patient eligibility

About

The purpose of this study is to assess the efficacy and safety in the real-world settings of glofitamab in combination with salvage therapy among Chinese adult patients with relapsed or refractory B-cell non-hodgkin lymphoma.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Be diagnosed as B-NHL
  • Relapse or refractory to previous treatment
  • Participants who will be treated with glofitamab

Exclusion criteria

  • Participant who currently participates in or with plan to participate in any interventional clinical trial
  • Any other reason that, in the investigator's opinion, makes the participant unsuitable to participate in this study.

Trial design

50 participants in 1 patient group

Observational Cohort
Treatment:
Drug: Glofitamab

Trial contacts and locations

1

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Central trial contact

Haiwen Huang

Data sourced from clinicaltrials.gov

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