Trials / Completed
CompletedNCT00113581
Safety Study of EMD 72000 in Combination With ECX (Epirubicin, Cisplatin and Capecitabine) in Oesophagogastric Cancer
A Phase I Study to Determine the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of Three Doses of Humanised EGFR Antibody EMD 72000 in Combination With ECX in Patients With Advanced Oesophagogastric Adenocarcinoma
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 26 (planned)
- Sponsor
- Merck KGaA, Darmstadt, Germany · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The main purpose of this study is to test the safety and tolerability and effectiveness of a new treatment, EMD 72000 (matuzumab), for advanced oesophagogastric cancer in combination with the chemotherapy regimen ECX (epirubicin, cisplatin and capecitabine). In addition the study will look at pharmacokinetic (how the the body takes up the drug) and pharmacodynamic parameters (what the drug does in the body).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | EMD 72000 (matuzumab) + ECX |
Timeline
- Start date
- 2002-10-01
- Primary completion
- 2006-05-01
- Completion
- 2007-01-01
- First posted
- 2005-06-10
- Last updated
- 2014-02-19
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT00113581. Inclusion in this directory is not an endorsement.