We assessed the tolerability, safety, pharmacokinetics and dose-limiting toxicity (DLT) of the recombinant humanized IgG4 anti-vascular endothelial growth factor (VEGF) monoclonal antibody, HuMV833, in patients with advanced cancer. Cohorts of patients with progressive solid tumours received escalating doses of HuMV833 as a 1-h intravenous, (I.V.) infusion on days 1, 15, 22, and 29. Twenty patients (median Eastern Cooperative Oncology Group (ECOG) score 1) were accrued. HuMV833 infusions were well tolerated and there were no grade III or IV toxicities definitely related to the antibody. Grade I or II toxicities probably related to the antibody included fatigue, dyspnoea and rash. There were two episodes of asymptomatic hypocalcaemia, one at...
Background MUC16 is a tumor-specific antigen overexpressed in ovarian (OC) and pancreatic (PC) cance...
This report presents results from the expansion cohort of the first-in-human, phase I trial of the n...
BACKGROUND: To report the nonrandomized first-in-human phase I trial of PRS-050, a novel, rationally...
Background: Vascular endothelial growth factor (VEGF) is apotent angiogenic cytokine, and various in...
Background: Vascular endothelial growth factor (VEGF) is a potent angiogenic cytokine, and various i...
LESSONS LEARNED: The novel therapeutic vaccine hVEGF(26-104) /RFASE was found to be safe and well to...
Lessons Learned: The novel therapeutic vaccine hVEGF26–104/RFASE was found to be safe and well toler...
PURPOSE: A first-in-human study was performed with MP0250, a DARPin drug candidate. MP0250 specifica...
Purpose: Objectives of this dose-finding study were to determine the MTD and recommended phase II do...
Purpose: This first-in-human study (NCT02947152) evaluated the safety, tolerability, pharmacokinetic...
PURPOSE: In previous studies, we have shown the potential of radioimmunotherapy (RIT) with (186)Re-l...
Purpose: In previous studies, we have shown the potential of radioimmunotherapy (RIT) with 186Re-lab...
The development of a neovascular supply (angiogenesis) is a major aspect of tumorigenesis. Recent wo...
BACKGROUND: Immune checkpoint blockade has demonstrated clinical benefits across multiple solid tumo...
BACKGROUND: This open-label, first-in-human, phase 1 study evaluated the safety, pharmacokinetics, p...
Background MUC16 is a tumor-specific antigen overexpressed in ovarian (OC) and pancreatic (PC) cance...
This report presents results from the expansion cohort of the first-in-human, phase I trial of the n...
BACKGROUND: To report the nonrandomized first-in-human phase I trial of PRS-050, a novel, rationally...
Background: Vascular endothelial growth factor (VEGF) is apotent angiogenic cytokine, and various in...
Background: Vascular endothelial growth factor (VEGF) is a potent angiogenic cytokine, and various i...
LESSONS LEARNED: The novel therapeutic vaccine hVEGF(26-104) /RFASE was found to be safe and well to...
Lessons Learned: The novel therapeutic vaccine hVEGF26–104/RFASE was found to be safe and well toler...
PURPOSE: A first-in-human study was performed with MP0250, a DARPin drug candidate. MP0250 specifica...
Purpose: Objectives of this dose-finding study were to determine the MTD and recommended phase II do...
Purpose: This first-in-human study (NCT02947152) evaluated the safety, tolerability, pharmacokinetic...
PURPOSE: In previous studies, we have shown the potential of radioimmunotherapy (RIT) with (186)Re-l...
Purpose: In previous studies, we have shown the potential of radioimmunotherapy (RIT) with 186Re-lab...
The development of a neovascular supply (angiogenesis) is a major aspect of tumorigenesis. Recent wo...
BACKGROUND: Immune checkpoint blockade has demonstrated clinical benefits across multiple solid tumo...
BACKGROUND: This open-label, first-in-human, phase 1 study evaluated the safety, pharmacokinetics, p...
Background MUC16 is a tumor-specific antigen overexpressed in ovarian (OC) and pancreatic (PC) cance...
This report presents results from the expansion cohort of the first-in-human, phase I trial of the n...
BACKGROUND: To report the nonrandomized first-in-human phase I trial of PRS-050, a novel, rationally...