Study to evaluate the safety and tolerability of intravenous ICVB-1042
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
17
Part A Dose Escalation to assess safety and tolerability of ascending dose levels, define the maximum tolerated dose (MTD), and expansion dose(s) Part B Dose Expansion to further assess safety and tolerability of 1 or more dose levels
California Cancer Associates
San Marcos, California, United States
Karmanos Cancer Institute
Detroit, Michigan, United States
NYU Langone Health, Perlmutter Cancer Center
New York, New York, United States
Safety of intravenous ICVB-1042
Assessment of treatment-emergent dose limiting toxicity
Time frame: From dose administration through 12 weeks
Concentration profile of ICVB-1042 in plasma
Time frame: Up to 48 hours after drug infusion
Determine immunogenicity of ICVB-1042
Assessment of anti-drug antibody titer
Time frame: From dose administration through 12 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of North Carolina Lineberger Comprehensive Cancer Center
Chapel Hill, North Carolina, United States
Carolina BioOncology
Huntersville, North Carolina, United States
University of Pennsylvania, Abramson Cancer Center
Philadelphia, Pennsylvania, United States
Sarah Cannon Research Institute
Nashville, Tennessee, United States
Next Oncology, Dallas
Irving, Texas, United States
Next Oncology, San Antonio
San Antonio, Texas, United States
Next Oncology, Virginia
Fairfax, Virginia, United States