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A Study of a Human Anti-Intercellular Adhesion Molecule-1 Monoclonal Antibody, in Patients With Multiple Myeloma

Phase 1
Completed
Conditions
Multiple Myeloma
Interventions
Biological: BI-505
Registration Number
NCT01025206
Lead Sponsor
BioInvent International AB
Brief Summary

This is a first in human study which will assess the safety and tolerability of a monoclonal antibody against ICAM-1 in patients with Multiple Myeloma. The tumour response rate will also be measured.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
35
Inclusion Criteria
  • Advanced Myeloma with measurable disease after at least 2 previous regimens.
  • Life expectancy > 3 months.
  • Performance status ECOG < 2.
Exclusion Criteria
  • Prior antineoplastic therapy within 4 weeks prior to inclusion.
  • No high dose steroids within 7 days prior to screening.
  • Severe other conditions.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
BI-505BI-505-
Primary Outcome Measures
NameTimeMethod
Safety assessed as Adverse Events, ECG, vital signs and clinical laboratory testsfour weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (7)

Rigshospitalet

πŸ‡©πŸ‡°

Copenhagen, Denmark

University of Utah Health Sciences Center, Department of Medicine, Division of Hematology, Utah Blood and Marrow Transplant and Myeloma Program

πŸ‡ΊπŸ‡Έ

Salt Lake City, Utah, United States

University of Maryland, Greenebaum Cancer Center

πŸ‡ΊπŸ‡Έ

Baltimore, Maryland, United States

Ghent University Hospital

πŸ‡§πŸ‡ͺ

Ghent, Belgium

AZ Sint-Jan

πŸ‡§πŸ‡ͺ

Brugge, Belgium

Karolinska University Hospital

πŸ‡ΈπŸ‡ͺ

Huddinge, Sweden

Hematology Clinic Cancer Division, SkΓ₯ne University Hospital

πŸ‡ΈπŸ‡ͺ

Lund, Sweden

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