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Study of Immune Responses in Patients With Metastatic Melanoma

Primary Purpose

Metastatic Melanoma

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
anti-OX40
Sponsored by
Providence Health & Services
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Melanoma focused on measuring Metastatic melanoma, anti-OX40, Immunostimulatory

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with measurable or evaluable unresectable, stage IV metastatic melanoma. Either histologic or cytologic diagnosis is acceptable.
  2. Eastern Cooperative Oncology Group (ECOG) performance status 0, or 1 (Appendix A.)
  3. Age 18 years or above.
  4. Laboratory values (performed within 28 days prior to enrollment) as follows:

    • WBC ≥2000/microliter
    • Absolute lymphocyte count >300/mm3
    • Serum creatinine <1.5 X upper limit of laboratory normal
    • Hgb >8g/dl (patients may be transfused to reach this level)
    • Hct > 24%
    • Platelets >100,000 cells/mm3
    • Total bilirubin <1.5 X upper limit of laboratory normal, unless due to Gilbert's disease
    • AST (SGOT)/ALT (SGPT) <2.5 X upper limit of laboratory normal
    • Alkaline phosphatase <2.5 X upper limit of laboratory normal
    • HIV Negative
    • Hepatitis B surface antigen Negative
    • Hepatitis C antibody Negative
  5. Women of childbearing potential must have a negative pregnancy test and must avoid becoming pregnant while on treatment. Men must avoid fathering a child while on treatment. This exclusion is required due to the unknown toxicities that anti-OX40 may have on the forming fetus, spermatogenesis or the nursing child. Also, because pregnancy may impair immune function it may limit the treatment efficacy.
  6. Ability to give informed consent and comply with the protocol. Patients with a history of psychiatric illness must be judged able to understand fully the investigational nature of the study and the risks associated with the therapy.
  7. No active bleeding.
  8. No clinical coagulopathy (INR <1.5, PT <16 seconds, PTT < 38 seconds).
  9. Anticipated lifespan greater than 12 weeks.
  10. Failed at least one prior medical therapy for metastatic melanoma.

Exclusion Criteria:

  1. Active infection.
  2. History of or active autoimmune disease.
  3. Prior mouse monoclonal antibody treatment.
  4. Pregnant or lactating women, as treatment involves unforeseeable risks to the embryo or fetus.
  5. Need for chronic maintenance oral steroids.
  6. Active brain metastatic disease. Treated brain metastases with surgery, gamma-knife radiosurgery and/or whole brain radiation and stable for at least 4 weeks and off steroids are eligible.
  7. Any medical or psychiatric condition that in the opinion of the PI would preclude compliance with study procedures.

Sites / Locations

  • Providence Portland Medical Center

Outcomes

Primary Outcome Measures

Increased number of tumor antigen specific circulating T Cells
T Cells will be harvested by apheresis at baseline and Day 15 following anti-OX40 administration.

Secondary Outcome Measures

Full Information

First Posted
August 12, 2011
Last Updated
March 6, 2013
Sponsor
Providence Health & Services
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1. Study Identification

Unique Protocol Identification Number
NCT01416844
Brief Title
Study of Immune Responses in Patients With Metastatic Melanoma
Official Title
Phase II Exploratory Study of Immune Responses in Patients With Metastatic Melanoma Treated With Mouse Monoclonal Anti-OX40
Study Type
Interventional

2. Study Status

Record Verification Date
March 2013
Overall Recruitment Status
Withdrawn
Why Stopped
Change in the development plan for the anti-OX40 antibody.
Study Start Date
September 2012 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Providence Health & Services

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In this study, anti-OX40 will be given to patients with melanoma to find out how the immune system responds to treatment with anti-OX40. It is hoped that this treatment will cause an immune response against melanoma resulting in tumor regression, but this is not known at this time. Anti-OX40 is a large protein that can help immune cells that fight bacteria, viruses and cancer cells.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Melanoma
Keywords
Metastatic melanoma, anti-OX40, Immunostimulatory

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
anti-OX40
Intervention Description
Patients with metastatic melanoma will be given 0.4 mg/kg anti-OX40 on days 1, 3 and 5 of a single treatment cycle.
Primary Outcome Measure Information:
Title
Increased number of tumor antigen specific circulating T Cells
Description
T Cells will be harvested by apheresis at baseline and Day 15 following anti-OX40 administration.
Time Frame
Screening (baseline) and Day 15

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with measurable or evaluable unresectable, stage IV metastatic melanoma. Either histologic or cytologic diagnosis is acceptable. Eastern Cooperative Oncology Group (ECOG) performance status 0, or 1 (Appendix A.) Age 18 years or above. Laboratory values (performed within 28 days prior to enrollment) as follows: WBC ≥2000/microliter Absolute lymphocyte count >300/mm3 Serum creatinine <1.5 X upper limit of laboratory normal Hgb >8g/dl (patients may be transfused to reach this level) Hct > 24% Platelets >100,000 cells/mm3 Total bilirubin <1.5 X upper limit of laboratory normal, unless due to Gilbert's disease AST (SGOT)/ALT (SGPT) <2.5 X upper limit of laboratory normal Alkaline phosphatase <2.5 X upper limit of laboratory normal HIV Negative Hepatitis B surface antigen Negative Hepatitis C antibody Negative Women of childbearing potential must have a negative pregnancy test and must avoid becoming pregnant while on treatment. Men must avoid fathering a child while on treatment. This exclusion is required due to the unknown toxicities that anti-OX40 may have on the forming fetus, spermatogenesis or the nursing child. Also, because pregnancy may impair immune function it may limit the treatment efficacy. Ability to give informed consent and comply with the protocol. Patients with a history of psychiatric illness must be judged able to understand fully the investigational nature of the study and the risks associated with the therapy. No active bleeding. No clinical coagulopathy (INR <1.5, PT <16 seconds, PTT < 38 seconds). Anticipated lifespan greater than 12 weeks. Failed at least one prior medical therapy for metastatic melanoma. Exclusion Criteria: Active infection. History of or active autoimmune disease. Prior mouse monoclonal antibody treatment. Pregnant or lactating women, as treatment involves unforeseeable risks to the embryo or fetus. Need for chronic maintenance oral steroids. Active brain metastatic disease. Treated brain metastases with surgery, gamma-knife radiosurgery and/or whole brain radiation and stable for at least 4 weeks and off steroids are eligible. Any medical or psychiatric condition that in the opinion of the PI would preclude compliance with study procedures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brendan D Curti, MD
Organizational Affiliation
Providence Health & Services
Official's Role
Principal Investigator
Facility Information:
Facility Name
Providence Portland Medical Center
City
Portland
State/Province
Oregon
ZIP/Postal Code
97213
Country
United States

12. IPD Sharing Statement

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Study of Immune Responses in Patients With Metastatic Melanoma

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