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Drug expired and access to additional supply ended. PI left the institution shortly afterwards and the study will not be re-activated. Only 4 patients were enrolled.
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| Name | Class |
|---|---|
| MedImmune LLC | INDUSTRY |
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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.
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).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 21 Days | Experimental | MEDI6469 0.4 mg/kg IV x 3 doses over 5-6 days starting 21 days prior to surgery |
|
| 14 Days | Experimental | MEDI6469 0.4 mg/kg IV x 3 doses over 5-6 days starting 14 days prior to surgery |
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| 7 Days | Experimental | MEDI6469 0.4 mg/kg IV x 3 doses over 5-6 days starting 7 days prior to surgery |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MEDI6469 | Drug | MEDI6469 0.4 mg/kg IV x 3 doses over 5-6 days |
|
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
| 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Pippa Newell, MD | Providence Health & Services | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Portland Providence Medical Center | Portland | Oregon | 97213 | United States |
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| Label | URL |
|---|---|
| Providence Cancer Center | View source |
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |