Safety and Efficacy Study With Catumaxomab in Patients After Curative Resection of a Gastric Adenocarcinoma

Sponsor

Neovii Biotech (Industry)

Overall Status

Completed

CT.gov ID

NCT00352833

Collaborator

(none)

Enrollment

Location

Duration (Months)

2.9

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Investigation of the outcome of an adjuvant treatment with catumaxomab as compared to surgery alone in patients after curative resection of a gastric adenocarcinoma in order to gain more detailed information primary on safety, tolerability and feasibility and secondary on relevant efficacy parameters.

Condition or Disease	Intervention/Treatment	Phase
Gastric Cancer Gastric Adenocarcinoma	Drug: catumaxomab	Phase 2

Detailed Description

A controlled, randomized, open-label, multi-center, parallel-group, Phase II study to generate valid hypotheses on safety and efficacy issues in patients with a primary confirmed diagnosis of gastric adenocarcinoma and a high risk of disseminated tumor cells due to serosal infiltration after curative gastrectomy. Eligible patients will be centrally randomized by IVRS during operation to one of the two study groups in an 1:1 ratio: surgery plus catumaxomab or surgery alone.

Treatment with catumaxomab will consist of an initial dose of 10 µg given intraoperatively as an intraperitoneal bolus on day 0 and of four following ascending doses (10-20-50-150 µg) which will be administered as an i.p.-infusion via a provided indwelling catheter on the days 7, 10, 13 and 16, respectively.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

40 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Multicenter, Open-Label and Randomized Phase II Study to Evaluate Safety and Efficacy of the Trifunctional Bispecific Antibody Catumaxomab (Anti-EpCAM x Anti-CD3) in Patients After Curative Resection of a Confirmed Gastric Adenocarcinoma Compared With Surgery Alone

Study Start Date :

Jul 1, 2006

Actual Study Completion Date :

Sep 1, 2007

Outcome Measures

Primary Outcome Measures

safety and efficacy data []

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Signed and dated informed consent
Patient has a primary diagnosis of a histologically confirmed gastric adenocarcinoma (including GE junction Siewert-Type 2 or 3)
Intended curative gastrectomy ('en-bloc´-R0-resection considering the standard D2-scheme)
Serosal infiltration (T3/T4, N+/-, M0) confirmed by immediate section with histopathologic assessment during surgery
Karnofsky index >= 70
Negative pregnancy blood test at screening in women with childbearing potential

Exclusion Criteria:

Presence of distant metastases
Macroscopic and microscopic residual tumor present after surgery
State after pancreas resection or thoracotomy
Exposure to prior cancer therapy or planned adjuvant chemo-or radiotherapy of the current gastric cancer
Previous treatment with non-humanized mouse or rat monoclonal antibodies
Known/suspected hypersensitivity to catumaxomab or similar antibodies
Any cancer disease or any cancer treatments within the last 5 years
Presence of constant immunosuppressive therapy
Inadequate renal function (creatinine > 1.5 x ULN)
Inadequate hepatic function (AST or ALT > 2.5 x ULN or bilirubin >= 1.5 x ULN)
Platelets < 75000 cells/mm³; absolute neutrophil count < 1500 cells/mm³
Patient had a bowel obstruction within the last 30 days
Pregnant or nursing woman, or woman of childbearing potential who is not using an effective contraceptive method during the study and at least contraceptives, intrauterine devices, double-barrier method, contraceptive patch, male partner sterilization or condoms)
Presence of any acute or chronic systemic infection
Any further condition which according to the investigator results in an undue risk to the patient during participating in the present study
Patient is an employee of any involved study investigator or any involved institution including the study sponsor
Parallel participation in another clinical trial or previous participation in this study
Treatment with another investigational product during this study or during the last 30 days prior to study start