CMP-001 in Combination With Nivolumab Compared to Nivolumab Monotherapy in Subjects With Advanced Melanoma

PHASE2/PHASE3TerminatedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

February 24, 2021

Primary Completion Date

July 22, 2024

Study Completion Date

July 22, 2024

Conditions
MelanomaAdvanced MelanomaMetastatic MelanomaUnresectable Melanoma
Interventions
DRUG

CMP-001

Subjects will receive CMP-001 10 mg IT weekly for 7 doses after which CMP-001 will be administered every 3 weeks (Q3W).

DRUG

Nivolumab

Nivolumab 360 mg IV is administered Q3W.

Trial Locations (20)

15232

University of Pittsburgh Medical Center / Hillman Cancer Center, Pittsburgh

19107

Thomas Jefferson University, Philadelphia

26506

West Virginia University, Morgantown

27710

Duke University Cancer Institute, Durham

30607

University Cancer & Blood Center, Athens

33331

Cleveland Clinic, Weston

40202

University of Louisville Health Care, Louisville

43210

The Ohio State University Wexner Medical Center, Columbus

52242

University of Iowa Hospitals & Clinics, Iowa City

72205

University of Arkansas for Medical Sciences, Little Rock

75246

Texas Oncology, Sammons Cancer Center, Dallas

85054

Mayo Clinic Arizona, Phoenix

90033

USC/Norris Comprehensive Cancer Center, Los Angeles

90095

University of California, Los Angeles, Los Angeles

92069

California Cancer Associates for Research & Excellence, Inc., San Marcos

92093

Moores Cancer Center at UC San Diego Health, La Jolla

92663

USC Norris Oncology/Hematology-Newport Beach, Newport Beach

98109

Seattle Cancer Care Alliance, Seattle

06106

Hartford Healthcare, Hartford

07960

Atlantic Health, Morristown

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

lead

Regeneron Pharmaceuticals

INDUSTRY

NCT04695977 - CMP-001 in Combination With Nivolumab Compared to Nivolumab Monotherapy in Subjects With Advanced Melanoma | Biotech Hunter | Biotech Hunter