Clinical Trials Directory

Trials / Unknown

UnknownNCT03800706

A Phase II Study to Evaluate the Safety and Efficacy of TQB2450 Injection in Relapsed or Refractory Classical Hodgkin's Lymphoma

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
85 (estimated)
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Single-Arm, Open-Label, Multicenter Clinical Trial. To observe the efficacy and safety of TQB2450 in patients of non-hodgkin lymphoma

Conditions

Interventions

TypeNameDescription
DRUGTQB2450TQB2450 is injectived (IV) every-3-weeks (Q3W) and it should be continued until disease progression or intolerable toxicity or patients withdrawal of consent, the longest use time of experimental drugs is 96 weeks.

Timeline

Start date
2019-03-25
Primary completion
2021-06-30
Completion
2021-12-31
First posted
2019-01-11
Last updated
2020-10-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03800706. Inclusion in this directory is not an endorsement.

A Phase II Study to Evaluate the Safety and Efficacy of TQB2450 Injection in Relapsed or Refractory Classical Hodgkin's (NCT03800706) · Clinical Trials Directory