Clinical Trials Directory

Trials / Terminated

TerminatedNCT04602065

Evaluation of Safety and Efficacy of IBI318 Monotherapy for Relapsed/Refractory Extranodal NK/T Cell Lymphoma (Nasal Type) Trial

Evaluation of Safety and Efficacy of IBI318 Monotherapy for Relapsed/Refractory Extranodal NK/T Cell Lymphoma (Nasal Type), a Multicenter, Open-label Phase Ib/II Trial

Status
Terminated
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
9 (actual)
Sponsor
Innovent Biologics (Suzhou) Co. Ltd. · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and efficacy of IBI318 monotherapy for relapsed/refractory extranodal NK/T cell lymphoma (nasal type).

Conditions

Interventions

TypeNameDescription
DRUGIBI318(Recombinant human anti-PD1/PD-L1 bispecific antibody)IBI318, 300mg, Q2W, Intravenous influsion.

Timeline

Start date
2020-11-24
Primary completion
2023-02-28
Completion
2023-02-28
First posted
2020-10-26
Last updated
2023-03-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04602065. Inclusion in this directory is not an endorsement.

Evaluation of Safety and Efficacy of IBI318 Monotherapy for Relapsed/Refractory Extranodal NK/T Cell Lymphoma (Nasal Typ (NCT04602065) · Clinical Trials Directory