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STING Agonist

ADU-S100 for Head and Neck Squamous Cell Carcinoma

Phase 2
Waitlist Available
Research Sponsored by Chinook Therapeutics, Inc. (formerly Aduro)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 25 months
Awards & highlights

Summary

ADU-CL-20 is an open-label, multicenter Phase 2 clinical trial to evaluate the efficacy and safety of intratumoral ADU-S100 (also referred to as MIW815) administered with pembrolizumab in the first-line setting. The population will consist of adults with PD-L1 positive recurrent or metastatic HNSCC.

Eligible Conditions
  • Head and Neck Squamous Cell Carcinoma
  • Head and Neck Cancers

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 25 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 25 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Evaluation of Clinical Activity by the Objective Response Rate (ORR; Complete Response [CR] and Partial Response [PR]) Per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1

Trial Design

1Treatment groups
Experimental Treatment
Group I: ADU-S100 and pembrolizumabExperimental Treatment1 Intervention
All eligible subjects will receive intravenous (IV) infusions of pembrolizumab and intratumoral injections of ADU-S100.

Find a Location

Who is running the clinical trial?

Chinook Therapeutics, Inc. (formerly Aduro)Lead Sponsor
1 Previous Clinical Trials
47 Total Patients Enrolled
Chinook Therapeutics, Inc.Lead Sponsor
8 Previous Clinical Trials
1,016 Total Patients Enrolled
~3 spots leftby Oct 2025