Anti-OX40 Antibody (MEDI6469) in Patients With Metastatic Colorectal Cancer

Colorectal Neoplasms Clinical Trial

Official title:

Phase I/Ib Study of Surgical Resection or Radiofrequency Ablation (RFA) of Metastatic Lesions in the Liver in Combination With Monoclonal Antibody to OX40 (MEDI6469) in Patients With Metastatic Colorectal Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02559024
• Other study ID #: 14-102A
• Status: Terminated
• Phase: Phase 1
• Start date: March 14, 2016
• Est. completion date: October 2018

Study information

• Verified date: January 2022
• Source: Providence Health & Services
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will test the ability of an immune modulator, anti-OX40 (MEDI6469) to alter the immune cell environment within colorectal cancer metastases. The drug will be administered to patients before surgical treatment.

Description:

There will be three distinct cohorts of patients which will vary the timing of the MEDI6469 dose, starting three weeks before surgery and decreasing the interval before surgery by one week with each cohort, as long as no dose-limiting toxicity attributable to the anti-OX40 are observed.

Immunohistochemistry will be used to measure the immune cells within primary and metastatic tumors when resected tissue is available, and surgically ablated tumors, giving each specimen an "immune score". The primary endpoint of the study will be the difference in immune scores of patients treated with anti-OX40 compared to historical controls (immune scores of untreated patients). Secondary endpoints will include both clinical (survival) and immunological data (specific measurements of immune cell populations based on flow cytometry and immunohistochemistry).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 4
• Est. completion date: October 2018
• Est. primary completion date: October 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients who will undergo staged liver resections are included in this study. In these cases, preoperative MEDI6469 will be given prior to the initial procedure.

• Patients with small <3 cm tumors located >2 cm away from central bile ducts will be considered for either radiofrequency ablation or resection, the choice of which will be determined at the time of surgery.

• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

• Laboratory values during preoperative assessment within the protocol specified range

• Ability to give informed consent and comply with the protocol. Patients with a history of psychiatric illness must be judged able to understand the investigational nature of the study and the risks associated with the therapy.

• No active gastrointestinal bleeding.

• No clinical or laboratory coagulopathy

• Anticipated lifespan greater than 12 weeks

Exclusion Criteria:

• Metastatic disease outside of the liver that is not considered surgically resectable or curable.

• Active infection.

• Active autoimmune disease including patients with Inflammatory Bowel Disease as determined by an autoimmune questionnaire.

• Previous treatment with mouse monoclonal antibodies.

• Need for chronic maintenance oral steroids.

• Any medical or psychiatric condition that in the opinion of the PI would preclude compliance with study procedures.

• Enrollment in a clinical trial in which a different investigational agent is administered within 4 weeks prior to the first dose of MEDI6469.

Related Conditions & MeSH terms

• Colorectal Neoplasms

Intervention

Drug:
• MEDI6469
MEDI6469 0.4 mg/kg IV x 3 doses over 5-6 days

Locations

Country	Name	City	State
United States	Portland Providence Medical Center	Portland	Oregon

Sponsors (2)

Lead Sponsor	Collaborator
Providence Health & Services	MedImmune LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety (side-effects or complications related to the study drug)	Patients are seen at least 7 times in clinic and have 3 physical exams and provide interim medical history four times to identify potential side-effects or complications related to the study drug.	48 Days
Primary	Immune Score	The number of CD8 effector T cells, CD4 regulatory T cells, the expression of activation markers OX40, CD38 and HLA-DR.	27 Days

External Links

•   Providence Cancer Center