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UnknownNCT05172856

A Phase Ib Study of Primary Efficacy and Safety of IBI321 Monotherapy or Combination Therapy in Patients With Advanced Solid Tumors

A Phase Ib, Open-Label, Multi-Center, Study of Primary Efficacy and Safety of IBI321 Monotherapy or Combination Therapy in Patients With Advanced Solid Tumors

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
110 (estimated)
Sponsor
Innovent Biologics (Suzhou) Co. Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is open-label, multicenter, Phase Ib study is designed to evaluate the Primary Efficacy and Safety of IBI321 Monotherapy or Combination Therapy in participants with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
DRUGIBI321IBI321 at a dose no higher than RP2D, D1 IV Q3W.

Timeline

Start date
2022-03-01
Primary completion
2023-06-30
Completion
2024-12-31
First posted
2021-12-29
Last updated
2021-12-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05172856. Inclusion in this directory is not an endorsement.

A Phase Ib Study of Primary Efficacy and Safety of IBI321 Monotherapy or Combination Therapy in Patients With Advanced S (NCT05172856) · Clinical Trials Directory