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Not Yet RecruitingNCT06389526

A Study of CHS-1000 in Participants With Advanced or Metastatic Solid Tumors

A Phase 1, Multicenter, Open-Label Study of CHS-1000 as a Single Agent and in Combination With Toripalimab-tpzi in Participants With Advanced or Metastatic Solid Tumors

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
48 (estimated)
Sponsor
Coherus Oncology, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of this trial is to assess the tolerability and safety of CHS-1000 alone and in combination with toripalimab-tpzi in participants with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
BIOLOGICALCHS-1000Specified dose on specified days
BIOLOGICALToripalimabSpecified dose on specified days

Timeline

Start date
2025-02-15
Primary completion
2028-05-30
Completion
2028-05-30
First posted
2024-04-29
Last updated
2024-09-19

Regulatory

Source: ClinicalTrials.gov record NCT06389526. Inclusion in this directory is not an endorsement.

A Study of CHS-1000 in Participants With Advanced or Metastatic Solid Tumors (NCT06389526) · Clinical Trials Directory