Phase 1b/2 study to assess the safety and efficacy of mitazalimab in combination with chemotherapy in patients with metastatic pancreatic ductal adenocarcinoma.
OPTIMIZE-1 is a phase 1b/2, open-label, multi-center study assessing the clinical efficacy of mitazalimab in combination with chemotherapy in patients with metastatic pancreatic ductal adenocarcinoma. The efficacy of intravenously administered mitazalimab in combination with the standard of care chemotherapy mFOLFIRINOX will be evaluated in patients with metastatic pancreatic ductal adenocarcinoma. Two dose levels of mitazalimab, 450 ug/kg and 900 ug/kg, are planned to be evaluated together with mFOLFIRINOX for determination of recommended phase 2 dose (RP2D) of mitazalimab in combination with mFOLFIRINOX before entering a dose expansion part with RP2D obtained. The expansion part will evaluate the clinical efficacy of mitazalimab in combination with mFOLFIRINOX assessing objective response rate (ORR), primary endpoint, as well as Progression-free survival (PFS) and Overall survival (OS). The dose expansion part includes a Simon´s two-stage design with an interim analysis for stop for futility or efficacy based on ORR.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
94
Mitazalimab administered intravenously every 14 days in combination with standard of care chemotherapy modified FOLFIRINOX.
Cliniques Universitaires St-Luc
Brussels, Belgium
Hospital Erasme
Brussels, Belgium
UZA Antwerp
Edegem, Belgium
Incidence of Dose Limiting Toxicities (DLTs) (Part 1: Phase 1b Dose escalation)
Number of patients experiencing DLTs
Time frame: From first dose to end of dose limiting toxicity period (Day 1-21)
Objective response rate (ORR) (Part 2: Phase 2 Dose expansion)
Proportion of patients achieving complete response or partial response at any time during the study
Time frame: From first dose to 28-56 days after end of study treatment
Type, frequency and severity of Adverse Events
Number of patients experiencing AEs. Number of events summarized by SOC and preferred term.
Time frame: From informed consent signed to 28-56 days after end of of study treatment
Anti-drug-antibody (ADA) titer in serum (tolerability)
Immunogenicity of mitazalimab
Time frame: From first dose until 28-56 days after end of study treatment
Cmax of mitazalimab (pharmacokinetics)
Cmax derived from mitazalimab serum concentrations
Time frame: From first dose until 28-56 days after end of study treatment
Tmax of mitazalimab (pharmacokinetics)
Tmax derived from mitazalimab serum concentrations
Time frame: From first dose until 28-56 days after end of study treatment
AUC(0-T) of mitazalimab (pharmacokinetics)
AUC(0-T) derived from mitazalimab serum concentrations
Time frame: From first dose until 28-56 days after end of study treatment
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Universitair Ziekenhuis Gent
Ghent, Belgium
Centre Hospitalier Universitaire de Bordeaux - Hôpital Haut-Lévêque,
Bordeaux, France
Centre Lyon Berard
Lyon, France
Institut Paoli-Calmettes
Marseille, France
Hopital Européen Georges Pompidou
Paris, France
Institute de Cancérologie de Lorraine
Vandœuvre-lès-Nancy, France
Hospital Universitario Vall d'Hebron, Barcelona, Spain
Barcelona, Spain
...and 4 more locations
Anti-tumor Activity per RECIST 1.1 guideline (efficacy)
Best overall response, duration of response, Duration of stable disease, disease control rate, Time to next anti-cancer therapy will be assessed
Time frame: From first dose until 28-56 days after end of study treatment
Progression free survival (efficacy)
Number of days from first dose of mitazalimab to progressive disease or death.
Time frame: From first dose and up to 2 years after end of study treatment
Overall survival (efficacy)
Number of days from first dose of mitazalimab until death
Time frame: From first dose and up to 2 years after end of study treatment