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Study of CHS-114 in Participants With Advanced Solid Tumors

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NCT05635643 · readout in 42 d

Sponsored by Coherus Oncology, Inc. (industry) · CHRS — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
87estimated
Sites
12
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-12-15actualWhen the study began enrolling
Primary completion2026-09-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-01-01estimatedThe whole study's end, after follow-up
First posted2022-12-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Advanced Solid Tumor
  • Head and Neck Squamous Cell Carcinoma

Interventions

  • Drug: CHS-114
  • Drug: toripalimab — also filed as Loqtorzi

Primary outcomes

what the primary-completion date above is the date OF
[Arms 1a, 1b, and 2] Rate of Dose Limiting Toxicity (DLT)
measured Assessed during first 21 days of treatment
[Arm 2] Summary of adverse events (AEs) based on treatment emergent AEs (TEAEs), anti-drug antibodies (ADA), and laboratory values.
measured Up to 24 months
[Arm 3] Safety and tolerability of CHS-114 in combination with toripalimab will be assessed by summarizing AEs and will be based on TEAEs as assessed by Common Terminology Criteria for Adverse Events (CTCAE) v5.0 or higher.
measured Up to 24 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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