Status:

COMPLETED

Study of ADH-1 Given Intravenously to Patients With Solid Tumors

Lead Sponsor:

Adherex Technologies, Inc.

Conditions:

Neoplasms

Eligibility:

All Genders

18+ years

Phase:

PHASE1

PHASE2

Brief Summary

N-cadherin, a protein involved in blood vessel cell binding, is increased as cancer progresses, and is on the surface of many tumor cells. ADH-1 blocks N-cadherin. This study will test the safety and ...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Signed written informed consent
  • Male and female patients \> or = 18 years of age with a solid tumor(s) refractory to standard curative therapy or for which no curative therapy exists. Study currently enrolling only patients with non-small cell lung cancer or advanced ovarian cancer to the safety expansion phase.
  • Clinically or radiologically documented measurable disease.
  • Immunohistochemical evidence of N-cadherin expression (at least 1+ positive) in archived or fresh tumor tissue
  • Adequate performance status and organ function, as evidenced by hematological and biochemical blood testing and electrocardiogram (ECG)
  • Exclusion criteria:
  • Receipt of ADH-1 prior to this clinical study
  • Chemotherapy, radiotherapy, or any other investigational drug within 30 days before study entry
  • History of primary brain tumors or brain metastases (known or suspected) unless any lesions have completely resolved following appropriate treatment and there has been no recurrence for at least 6 months. History of spinal cord compression. History of tumors that have shown clinically significant evidence of active bleeding (e.g., gross hemoptysis, hematemesis, hematuria, melena, or bleeding superficial tumor) within 12 weeks before study entry.
  • Stroke, major surgery, or other major tissue injury within 30 days before study entry
  • History of congestive heart failure, myocardial infarction, angina, life threatening arrhythmias, significant electrocardiogram (ECG) abnormalities, or known hypercoagulable states

Exclusion

    Key Trial Info

    Start Date :

    June 1 2005

    Trial Type :

    INTERVENTIONAL

    End Date :

    January 1 2008

    Estimated Enrollment :

    Patients enrolled

    Trial Details

    Trial ID

    NCT00265057

    Start Date

    June 1 2005

    End Date

    January 1 2008

    Last Update

    December 28 2010

    Active Locations (3)

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    Page 1 of 1 (3 locations)

    1

    Istituto Nazionale per lo Studio e la Cura dei Tumori

    Milan, Italy, 20133

    2

    Instituto Europeo di Oncologia

    Milan, Italy, 20141

    3

    Istituto Oncologico della Svizzera Italiana

    Bellinzona, Switzerland, 6500