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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01546571
Other study ID # 103A-301
Secondary ID
Status Terminated
Phase Phase 3
First received
Last updated
Start date May 1, 2012
Est. completion date June 30, 2021

Study information

Verified date December 2021
Source Polynoma LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine how safe and how well POL-103A works in preventing the relapse of melanoma after patients who have undergone surgery.


Recruitment information / eligibility

Status Terminated
Enrollment 504
Est. completion date June 30, 2021
Est. primary completion date April 29, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Histologically confirmed Stage IIb, IIc, III melanoma - Surgical resection within 90 days of first dosing - Persons with positive sentinel nodes must have a complete lymphadenectomy - ECOG performance status 0 or 1 Exclusion Criteria: - Any prior melanoma treatment other than surgery or regional irradiation - Use of biologic response modifiers within 60 days of first dosing - Subjects with history of other malignancy within past 5 years (with exceptions)

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
POL-103A
POL-103A is administered intradermally, divided into 4 injections (0.2 mL each injection) into the volar surface of forearms and into the anterior upper thighs
POL-103A without API
Placebo is administered intradermally, divided into 4 injections (0.2 mL each injection) into the volar surface of forearms and into the anterior upper thighs

Locations

Country Name City State
Canada CISSS de la Montérégie - Centre Greenfield Park Quebec
Canada Royal Victoria Hospital Montreal Quebec
Canada Durham Regional Cancer Centre Oshawa Ontario
Canada CHU de Quebec-L'Hotel-Dieu de Quebec Quebec
Canada Princess Margaret Hospital, Department of Medical Oncology Toronto Ontario
Canada BCCA Vancouver Island Cancer Centre Victoria British Columbia
United States Anschutz Cancer Pavilion Aurora Colorado
United States Harry & Jeanette Weinberg Cancer Institute @ Franklin Square Baltimore Maryland
United States Bend Memorial Clinic Bend Oregon
United States Beverly Hills Cancer Center Beverly Hills California
United States Ironwood Cancer and Research Centers Chandler Arizona
United States University of Virginia Hospital Charlottesville Virginia
United States The Cleveland Clinic Foundation Cleveland Ohio
United States Baylor Research Institute Dallas Texas
United States Cancer Solutions Dallas Texas
United States Premier Health Partners Clinical Trials Research Alliance Dayton Ohio
United States City of Hope National Medical Center Duarte California
United States Inova Schar Cancer Center Fairfax Virginia
United States Highlands Oncology Group Fayetteville Arkansas
United States The West Clinic P.C. d/b/a West Cancer Center Germantown Tennessee
United States East Carolina University Greenville North Carolina
United States John Theurer Cancer Center/ Hackensack Medical Center Hackensack New Jersey
United States Center for Clinical Studies Houston Texas
United States Independence Family Health Center (Cleveland Clinic) Independence Ohio
United States Investigative Clinical Research of Indiana Indianapolis Indiana
United States University of Iowa Hospitals and Clinics Iowa City Iowa
United States Cancer Specialists of North Florida Jacksonville Florida
United States GenesisCare USA of Florida Jacksonville Florida
United States Center for Pharmaceutical Research Kansas City Missouri
United States University of Tennessee Medical Center Knoxville Tennessee
United States Norris Cotton Cancer Center / Dartmouth-Hitchcock Medical Center Lebanon New Hampshire
United States Baptist Health Lexington Lexington Kentucky
United States Central Kentucky Research Associates Lexington Kentucky
United States University of Arkansas for Medical Sciences Little Rock Arkansas
United States The Angeles Clinic and Research Institute Los Angeles California
United States UCLA Hematology & Oncology Clinic Los Angeles California
United States University of Louisville Louisville Kentucky
United States Hillcrest Hospital (Cleveland Clinic) Mayfield Heights Ohio
United States Mount Sinai Medical Center Miami Beach Florida
United States University of Minnesota Masonic Cancer Institute Minneapolis Minnesota
United States Intermountain Medical Center Murray Utah
United States Rutgers Cancer Institute of NJ New Brunswick New Jersey
United States Mount Sinai School of Medicine New York New York
United States Advocate Medical Group Niles Illinois
United States MD Anderson Cancer Center-Orlando Orlando Florida
United States Ameriderm Research Ormond Beach Florida
United States Ventura County Hematology Oncology Specialists Oxnard California
United States Thomas Jefferson Medical Oncology Philadelphia Pennsylvania
United States Oregon Health and Science University Portland Oregon
United States Providence Portland Medical Center Portland Oregon
United States Mayo Clinic Cancer Center, Mayo Clinic Rochester Rochester Minnesota
United States Sutter Cancer Center Sacramento California
United States MediSearch Clinical Trials Saint Joseph Missouri
United States St. Louis University Hospital Saint Louis Missouri
United States Washington University School of Medicine Saint Louis Missouri
United States The Huntsman Cancer Institute, University of Utah Health Care Salt Lake City Utah
United States St. Mary's Hospital & Medical Center Department of Pathology San Francisco California
United States Virginia Mason Medical Center Seattle Washington
United States Ascension Providence Hospital Southfield Michigan
United States Southern Illinois University School of Medicine Springfield Illinois
United States Multicare Institute for Research & Innovation Tacoma Washington
United States University of Arizona Cancer Center Tucson Arizona
United States The Melanoma Center at the Washington Cancer Institute Washington District of Columbia
United States McGlinn Cancer Institute, Reading Hospital West Reading Pennsylvania
United States Wake Forest University School of Medicine, Comprehensive Cancer Center Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Polynoma LLC

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence Free Survival (RFS) This is an event driven trial. Recurrence-free survival time (RFS) is computed from the earliest of the date of recurrence or death or, if without recurrence or death, the date last assessed for recurrence without diagnosis of recurrence (censored). The date of recurrence is specified as the first date a recurrence is suspected, which is later confirmed by biopsy. 436 events or approximately 4 years
Secondary Overall Survival (OS) Survival time is computed based on the date of death if the subject is known dead or the date last known to be alive (censored). Zero time is the date of randomization. 432 events or approximately 10 years
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