Clinical Trials Directory

Trials / Terminated

TerminatedNCT02908451

A Study of AbGn-107 in Patients With Gastric, Colorectal, Pancreatic or Biliary Cancer

A Phase I Dose Escalation Study, With Cohort Expansion, to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of AbGn-107 Therapy in Patients With Chemo-refractory Locally Advanced, Recurrent, or Metastatic Gastric, Colorectal, Pancreatic or Biliary Cancer

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
39 (actual)
Sponsor
AbGenomics B.V Taiwan Branch · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is to define the safety profile and to determine the Maximal tolerated dose regimen and preliminary efficacy of AbGn-107 administered every 14 days (Q2W regimen) or 28 days (Q4W regimen) in patients with chemo-refractory locally advanced, recurrent or metastatic gastric, colorectal, pancreatic or biliary cancer.

Detailed description

AbGn-107 is an antibody drug conjugate (ADC) which targets an antigen (AG7 antigen) present in gastric, colorectal, pancreatic cancer or biliary cancer. This study is a standard 3 + 3 dose escalation design with cohort expansion. AbGn-107 will be administered every 14 days (Q2W regimen) or 28 days (Q4W regimen) in patients with chemo-refractory locally advanced, recurrent or metastatic gastric, colorectal, pancreatic adenocarcinoma or biliary cancer. The primary objectives of this study are to define the safety profile and to determine the maximum tolerated dose regimen of AbGn-107, and the secondary objectives are to evaluate the pharmacokinetic (PK) parameters, the immunogenicity, and preliminary efficacy of AbGn-107.

Conditions

Interventions

TypeNameDescription
BIOLOGICALAbGn-107Antibody Drug Conjugate

Timeline

Start date
2017-04-24
Primary completion
2021-02-28
Completion
2021-02-28
First posted
2016-09-21
Last updated
2021-07-13

Locations

9 sites across 2 countries: United States, Taiwan

Regulatory

Source: ClinicalTrials.gov record NCT02908451. Inclusion in this directory is not an endorsement.