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Brief Title: TrasGEX™: Phase 1 Study in Cancer Patients
Official Title: A Phase I Dose-Escalation and Pharmacokinetic Study of TrasGEX™ in Patients With Locally Advanced or Metastatic HER-2-positive Cancer
Study ID: NCT01409343
Brief Summary: This was a prospective, open label, multicenter study evaluating the safety, tolerability and pharmacokinetics of TrasGEX™ after intravenous administration in patients with HER-2 positive cancers. The effect of TrasGEX™ on the development of anti-drug antibodies and on tumour response was also evaluated.
Detailed Description: Adult patients with advanced and/or metastatic HER2-positive cancer who were resistant to or for whom there was no standard anti-tumor therapy available at the time of enrollment and who had an estimated life expectancy of at least 3 months were eligible for participation in this study. Patients were to receive the study drug until disease progression (clinical or radiologic), unacceptable toxicity, or any other reason leading to termination of study treatment. Dose-escalation was performed in 3 to 6-patient cohorts.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Glycotope Investigational Site, Graz, , Austria
Glycotope Investigational Site, Innsbruck, , Austria
Glycotope Investigational Site, Hamburg, , Germany
Glycotope Investigational Site, Milan, , Italy
Glycotope Investigational Site, Bellinzona, , Switzerland
Name: Glycotope GmbH
Affiliation: Glycotope GmbH
Role: STUDY_DIRECTOR