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Suspended Phase 1 Interventional

CA-4948 Added to Standard Chemotherapy to Treat Metastatic or Unresectable Pancreatic Cancer

ClinicalTrials.gov ID: NCT05685602

Public ClinicalTrials.gov record NCT05685602. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 11:02 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I Clinical Trial of CA-4948 in Combination With Gemcitabine and Nab-Paclitaxel in Metastatic or Unresectable Pancreatic Ductal Carcinoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase I trial tests the safety, side effects, and best dose of emavusertib (CA-4948) in combination with gemcitabine and nab-paclitaxel in treating patients with pancreatic ductal adenocarcinoma that has spread from where it first started (primary site) to other places in the body (metastatic) or cannot be removed by surgery (unresectable). CA-4948 is in a class of medications called kinase inhibitors. It works by blocking the action of abnormal proteins called interleukin-1 receptor-associated kinase 4 (IRAK4) and FMS-like tyrosine kinase 3 (FLT3) that signal cells to multiply. This may help keep cancer cells from growing. The usual approach for patients with pancreatic ductal adenocarcinoma is treatment with chemotherapy drugs gemcitabine and nab-paclitaxel. Gemcitabine is a chemotherapy drug that blocks the cells from making DNA and may kill cancer cells. Paclitaxel is in a class of medications called anti-microtubule agents. It stops cancer cells from growing and dividing and may kill them. Nab-paclitaxel is an albumin-stabilized nanoparticle formulation of paclitaxel which may have fewer side effects and work better than other forms of paclitaxel. Giving CA-4948 in combination with gemcitabine and nab-paclitaxel may shrink or stabilize metastatic or unresectable pancreatic ductal adenocarcinoma.

Study identification

NCT ID
NCT05685602
Recruitment status
Suspended
Study type
Interventional
Phase
Phase 1
Enrollment
43 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 12, 2023 (Actual)
Primary completion
Apr 30, 2027 (Estimated)
Completion
Apr 30, 2027 (Estimated)
Last update posted
Sep 9, 2026

2023 – 2027

United States locations

U.S. sites
26
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
City of Hope Comprehensive Cancer Center Duarte California 91010 —
UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care Irvine California 92612 —
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California 92868 —
UCHealth University of Colorado Hospital Aurora Colorado 80045 —
Northwestern University Chicago Illinois 60611 —
Memorial Hospital East Shiloh Illinois 62269 —
University of Kentucky/Markey Cancer Center Lexington Kentucky 40536 —
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287 —
National Cancer Institute Developmental Therapeutics Clinic Bethesda Maryland 20892 —
National Institutes of Health Clinical Center Bethesda Maryland 20892 —
Siteman Cancer Center at Saint Peters Hospital City of Saint Peters Missouri 63376 —
Siteman Cancer Center at West County Hospital Creve Coeur Missouri 63141 —
Washington University School of Medicine St Louis Missouri 63110 —
Siteman Cancer Center-South County St Louis Missouri 63129 —
Siteman Cancer Center at Christian Hospital St Louis Missouri 63136 —
NYU Langone Hospital - Long Island Mineola New York 11501 —
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York New York 10016 —
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center New York New York 10032 —
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599 —
University of Cincinnati Cancer Center-UC Medical Center Cincinnati Ohio 45219 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
University of Cincinnati Cancer Center-West Chester West Chester Ohio 45069 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
University of Wisconsin Carbone Cancer Center - Eastpark Medical Center Madison Wisconsin 53718 —
University of Wisconsin Carbone Cancer Center - University Hospital Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05685602, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 9, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05685602 live on ClinicalTrials.gov.

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