Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT05290597

A Phase 1, Open-label, Multicenter, Dose Escalation Study of IBI363 (PD1-IL2m) in Subjects With Advanced Solid Malignancies or Lymphomas

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Innovent Biologics (Suzhou) Co. Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a Phase 1, open-label, multicenter, dose-escalation study designed to evaluate the safety, tolerability, and DLTs to establish the maximum tolerated dose (MTD) or maximum administered dose (MAD), and the RP2D of sequential doses of IBI363 (study drug) in subjects with advanced, refractory solid malignancies or lymphomas.

Conditions

Interventions

TypeNameDescription
BIOLOGICALIBI363a mutated IL-2 cytokine fused to an anti-PD-1 antibody to combine IL-2 pathway stimulation with checkpoint blockade.

Timeline

Start date
2022-08-22
Primary completion
2026-01-28
Completion
2026-12-31
First posted
2022-03-22
Last updated
2026-03-05

Locations

4 sites across 1 country: Australia

Source: ClinicalTrials.gov record NCT05290597. Inclusion in this directory is not an endorsement.