A Study of exoASO-STAT6 (CDK-004) in Patients With Advanced Hepatocellular Carcinoma (HCC) and Patients With Liver Metastases From EIther Primary Gastric Cancer or Colorectal Cancer (CRC)

NCT05375604 | Terminated Phase 1 FDA Drug

• 1 other identifier: CDK-004-101
• Study Type: interventional
• Target: 9
• Locations: 1 country
• Sites: 3

Brief Summary

This is a first-in-human, Phase 1 open-label, multicenter, dose escalation, safety, pharmacodynamic, and PK study of exoASO-STAT6 (CDK-004) in patients with advanced Hepatocellular Carcinoma (HCC) and patients with liver metastases from either primary gastric cancer or colorectal cancer (CRC).

Conditions

Advanced Hepatocellular Carcinoma (HCC); Gastric Cancer Metastatic to Liver; Colorectal Cancer Metastatic to Liver

Outcome Measures

Primary Outcomes (1)

• To characterize the safety and tolerability of CDK-004.

  Incidence of treatment-emergent adverse events as assessed by CTCAE 5.0.

  Up to 2 years

Study Arms (1)

Experimental CDK-004

EXPERIMENTAL

CDK-004 administered as a single agent intravenously (IV) on Days 1 and 15 of Cycles 1 and 2, on Day 1 of every Cycle.

Drug: CDK-004

Interventions

CDK-004 DRUG

ASO-STAT6 exosome administered Intravenously

Also known as: exoASO-STAT6

Experimental CDK-004

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Must have one of the following cancer types:
• Advanced HCC defined as Barcelona Clinic Liver Cancer (BCLC) Stage B/C not amenable to resection or locoregional therapy;
• Histologic or radiologic proof of liver metastasis from primary CRC which is unresectable with no evidence of extrahepatic metastasis;
• Histologic or radiologic proof of liver metastasis from primary gastric cancer which is unresectable with no evidence of extrahepatic metastasis.
• Documented progression after at least 1 line of FDA approved systemic therapy for advanced HCC/gastric cancer/CRC or intolerable/refuse to chemotherapy.
• ≥ 18 years of age at screening.
• Measurable disease by RECIST v1.1.
• Able to provide archival tumor tissue/fresh biopsy prior to study treatment and on-treatment tumor biopsies if considered safe and medically feasible by the Investigator.
• ECOG performance status of 0-2.
• Acceptable liver function
• Acceptable renal function
• Acceptable hematologic status
• Cirrhosis classified as Child-Pugh Class A (applicable only to patients diagnosed with cirrhosis)..
• Women of child-bearing potential agree to use highly effective contraceptive methods and avoid egg donation and preservation during the study treatment and for 6 months after the last dose of study drug.
• Men of child-producing potential agree to use highly effective contraceptive methods and avoid sperm donation and preservation during the study treatment and for 6 months after the last dose of study drug.

You may not qualify if:

• Treatment with any systemic or liver-directed anticancer therapy within 3 weeks of the first dose of study drug.
• Uncontrolled partial or complete biliary obstruction.
• Left ventricular ejection fraction (LVEF) \< 50% at Screening.
• lead ECG demonstrating QT interval corrected by Fridericia's formula (QTcF) \> 480 ms or history of long QTc syndrome.
• Ongoing, clinically significant AEs due to prior anticancer therapies.
• Patients with history of another primary cancer, including co-existent second malignancy, with the exception of: a) curatively resected non-melanoma skin cancer; b) curatively treated cervical carcinoma in situ; or c) other primary solid tumor with no known active disease present or in the opinion of the Investigator will not affect patient outcome.
• Known clinically active brain metastases or known carcinomatous meningitis/leptomeningeal disease.
• Known clinically significant infection.
• Known clinically significant cardiac disease, including unstable angina or has had a procedure to address the underlying cause and has experienced angina within 4 weeks prior to Cycle 1 Day 1, acute myocardial infarction within 6 months from Day 1 of study drug administration, or New York Heart Association Class III or IV congestive heart failure.
• Known history of human immunodeficiency virus (HIV).
• If history of concurrent Hepatitis B virus (HBV) or Hepatitis C virus (HCV) infection, meets the following criteria: patients with detectable hepatitis B surface antigen (HbsAg) or detectable HBV DNA should be managed per local treatment guidelines. Controlled (treated) hepatitis B patients will be allowed if they started treatment at the time of consent and treatment is continued during study participation; patients with hepatitis C and detectable RNA are eligible if antiviral therapy has been completed prior to first administration of study drug. Testing does not need to be conducted at Screening if results from testing within the past 12 months are available.
• History of liver transplant.
• History of immunodeficiency or is receiving chronic systemic steroid therapy
• Poorly controlled diabetes mellitus.
• Active or previously documented autoimmune or inflammatory diseases

Sponsors & Collaborators

• Codiak BioSciences: lead

Study Sites (3)

City of Hope National Medical Center

Duarte, California, 91010, United States

Location

Memorial Sloan Kettering Cancer Center

New York, New York, 10065, United States

Location

Sarah Cannon Research Institute

Nashville, Tennessee, 37203, United States

Location

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 11, 2022
• First Posted: May 16, 2022
• Study Start: June 28, 2022
• Primary Completion: May 25, 2023
• Study Completion: May 30, 2023
• Last Updated: June 1, 2023

Record last verified: 2023-05

Data Sharing

• IPD Sharing: Will not share

Locations

US (3)