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Clinical Trials in the UK / NCT06608927
Active, not recruiting Phase 3

Study of Quemliclustat and Chemotherapy Versus Placebo and Chemotherapy in Patients With Metastatic Pancreatic Ductal Adenocarcinoma

NCT06608927 · tracked via the Priya Life Science UK tracker
Sponsor
Arcus Biosciences, Inc.
Phase
Phase 3
Started
2024-12-13
Last updated
2026-09-02

Condition(s) studied

Metastatic Pancreatic Ductal Adenocarcinoma

Investigational drug(s) / intervention(s)

QuemliclustatPlaceboNab-paclitaxelGemcitabine

Quemliclustat: Administered as specified in the treatment arm

Placebo: Administered as specified in the treatment arm

Nab-paclitaxel: Administered as specified in the treatment arm

Gemcitabine: Administered as specified in the treatment arm

Study summary

The purpose of this study is to compare overall survival of quemliclustat, nab-paclitaxel and gemcitabine versus placebo, nab-paclitaxel and gemcitabine in all randomized patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Have histologically or cytologically confirmed PDAC that is metastatic. * Have not been previously treated for PDAC in the metastatic setting. 1. Prior neoadjuvant and/or adjuvant therapy for PDAC is permitted if completed at least 12 months before randomization. 2. Prior palliative radiotherapy is allowed if completed at least 2 weeks prior to randomization and AEs have resolved to Grade 1 or less before randomization. 3. Prior and/or placement of a biliary stent/tube is permitted if any treatment-related AEs have improved to Grade ≤ 1 and the patient is not exhibiting any signs/symptoms of biliary obstruction. * Eastern Cooperative Oncology Group PS of 0 to 1. * At least 1 target lesion measurable by computed tomography (CT)/magnetic resonance imaging (MRI) per RECIST v1.1. not within a field of prior radiation therapy. Exclusion Criteria: * Previously treated for locally advanced, unresectable PDAC. * History of brain metastases or leptomeningeal metastases. * Prior treatment with a CD73 antagonist or inhibitor. * Underlying medical conditions that, in the investigator or sponsor's opinion, will make the administration of study-specified therapy hazardous NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

Primary outcome measure(s)

Trial sites (111)

FacilityCityRegionStatus
Research Site Phoenix Arizona
Research Site Tucson Arizona
Research Site La Jolla California
Research Site Los Alamitos California
Research Site Los Angeles California
Research Site Roseville California
Research Site San Francisco California
Research Site Santa Monica California
Research Site Denver Colorado
Research Site New Haven Connecticut
Research Site Jacksonville Florida
Research Site Miami Florida
Research Site Atlanta Georgia
Research Site Atlanta Georgia
Research Site Arlington Heights Illinois
Research Site Chicago Illinois
Research Site Indianapolis Indiana
Research Site Wichita Kansas
Research Site Baton Rouge Louisiana
Research Site Ann Arbor Michigan
Research Site Grand Rapids Michigan
Research Site Minneapolis Minnesota
Research Site Rochester Minnesota
Research Site Hattiesburg Mississippi
Research Site Kansas City Missouri
Research Site Omaha Nebraska
Research Site New Brunswick New Jersey
Research Site Buffalo New York
Research Site New York New York
Research Site New York New York
Research Site New York New York
Research Site New York New York
Research Site Rochester New York
Research Site Cleveland Ohio
Research Site Oklahoma City Oklahoma
Research Site Philadelphia Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site Nashville Tennessee
Research Site Austin Texas
Research Site Dallas Texas

+ 71 more sites — see the full list on the official registry below.

More Arcus Biosciences, Inc. trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06608927 on ClinicalTrials.gov ↗ ← All trials in the UK