GIM-122 is a first-in-class, humanized immunoglobulin G1 kappa dual functioning monoclonal antibody (DFA). This phase 1 / 2 study plans to evaluate the safety, tolerability, pharmacokinetics and clinical efficacy of intravenous (IV) administration of GIM-122 in adults with advanced malignancies.
This is a Phase 1/2, open label, first-in-human (FIH), multicenter, dose escalation study with enrichments and dose expansion cohorts at RP2D, designed to evaluate the safety, tolerability, PK, pharmacodynamics, and preliminary antitumor activity of GIM-122 administered as a single agent in adults with advanced solid malignancies. This study will be conducted in 2 parts: Phase 1 or Part A (dose escalation and enrichment) and Phase 2 or Part B (dose optimization and cohort expansion).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
111
GIM-122 administered IV once every 3 weeks or every 2 weeks
The Angeles Clinic and Research Institute
Los Angeles, California, United States
RECRUITINGUSC/Norris Comprehensive Cancer Center
Los Angeles, California, United States
RECRUITINGDose limiting toxicities [DLT] with GIM-122
To identify dose limiting toxicities \[DLT\] with GIM-122
Time frame: 18 months
Maximum tolerated dose [MTD] of GIM-122
To identify maximum tolerated dose \[MTD\] of GIM-122
Time frame: 18 months
Recommended Phase 2 Dose [RP2D] of GIM-122
To identify Recommended Phase 2 Dose \[RP2D\] of GIM-122
Time frame: 18 Months
Overall response rate (ORR) -Part B of the study
To identify overall response rate (ORR) in patients with advanced malignant tumors who are refractory/ resistant to PD-1 and PD-L1 therapy
Time frame: 36 months
Anti-tumor activity of GIM-122
To assess anti-tumor activity of GIM-122 as a single agent in patients with advanced malignant tumors who are refractory/ resistant to PD-1 and PD-L1 therapy
Time frame: 36 months
Incidence and severity of AE / SAEs and tolerability
To assess incidence and severity of AE / SAEs and tolerability assessed by CTCAE grading
Time frame: 36 months
Area under the plasma concentration versus time curve (AUC)
To preliminarily evaluate the AUC in patients with advanced malignant tumors
Time frame: 36 months
Peak Plasma Concentration (Cmax)
To preliminarily evaluate Cmax in patients with advanced malignant tumors
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UCLA Hematology/Oncology
Los Angeles, California, United States
RECRUITINGUCSF Helen Diller Family Comprehensive Cancer Center
San Francisco, California, United States
RECRUITINGFlorida Cancer Specialists
Sarasota, Florida, United States
RECRUITINGNorton Cancer Institute
Louisville, Kentucky, United States
RECRUITINGRutgers Cancer Institute of NJ
New Brunswick, New Jersey, United States
RECRUITINGTennessee Oncology, PLLC
Nashville, Tennessee, United States
RECRUITINGTexas Oncology - Baylor Sammons Cancer Center
Dallas, Texas, United States
RECRUITINGNEXT Oncology Dallas
Irving, Texas, United States
RECRUITING...and 1 more locations
Time frame: 36 months
Time of peak plasma concentration (Tmax)
To preliminarily evaluate Tmax in patients with advanced malignant tumors
Time frame: 36 months
Overall Response Rate (ORR) - Part A of the study
To preliminarily evaluate ORR in patients with advanced malignant tumors
Time frame: 36 months
Duration of response (DOR)
To preliminarily evaluate DOR in patients with advanced malignant tumors
Time frame: 36 months
Disease control rate (DCR)
To preliminarily evaluate DCR in patients with advanced malignant tumors
Time frame: 36 months
Best overall response (BOR)
To preliminarily evaluate BOR in patients with advanced malignant tumors
Time frame: 36 months
Progression-free survival (PFS)
To preliminarily evaluate PFS in patients with advanced malignant tumors
Time frame: 36 months
Overall survival (OS) rates at 12 months
To preliminarily evaluate OS in patients with advanced malignant tumors at 12 Months
Time frame: 36 months
Tumor expression of immunological markers
To analyze tumor expression of immunological markers
Time frame: 36 months