A Study of AMG 557 in Adults With Systemic Lupus Erythematosus

Systemic Lupus Erythematosus Clinical Trial

Official title:

A Randomized, Double-blind, Placebo-controlled, Ascending, Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 557 in Subjects With Systemic Lupus Erythematosus

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00774943
• Other study ID #: 20060169
• Status: Completed
• Phase: Phase 1
• First received: October 16, 2008
• Last updated: April 5, 2013
• Start date: December 2008
• Est. completion date: May 2012

Study information

• Verified date: April 2013
• Source: Amgen
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health CanadaUnited Kingdom: Medicines and Healthcare Products Regulatory AgencyUnited States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a Phase 1, randomized, placebo-controlled, double-blind, dose-escalation study of repeat SC doses of AMG 557 in adults with Systemic Lupus Erythematosus.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 58
• Est. completion date: May 2012
• Est. primary completion date: May 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Before any study-specific procedure, the appropriate written informed consent must be obtained;

• Men and women, between the ages of 18 and 70 years old, inclusive, at the time of randomization;

• Diagnosis of SLE as defined by the most recent ACR criteria, including a positive ANA at screening or documented positive ANA (the titer should be at least 1:80) in the past.

• SLE duration of at least six months, as diagnosed by a physician;

• Stable disease, defined as no change in SLE therapy within the previous 30 days; and, in the opinion of the investigator, no anticipated need for a change in SLE therapy will be required while the subject is enrolled in the study;

• Normal or clinically acceptable ECG (12-lead reporting ventricular rate and PR, QRS, QT, QTc) at screening and Day -1 based on the opinion of the investigator;

• Body mass index from 18 to 40 kg/m2 at screening;

• Able and willing to complete entire study according to study schedule.

• Immunizations up to date, with a minimum of tetanus, diphtheria, pertussis (td/Tdap), pneumococcal (polysaccharide) and influenza (during flu season) vaccinations, as determined by the Principal Investigator.

Exclusion Criteria:

• Positive serology for HIV antibodies, hepatitis B surface antigen or hepatitis C antibodies (confirmed by PCR or RIBA);

• Have had signs or symptoms of a viral, bacterial or fungal infection within 30 days of study randomization;

• Evidence of active or latent tuberculosis as assessed by PPD or Quantiferon testing at screening;

• Have donated blood or experienced a loss of blood >500mL within 4 weeks of randomization;

• History of ethanol or drug abuse within the last one year prior to randomization;

• Evidence of significant renal insufficiency, defined by:

The glomerular fitration rate < 50 mL/min using the Cockroft and Gault equation;

• Evidence of liver disease (eg, serum ALT or AST > 2x upper limit of normal);

• Total WBC <3000 x 106/L;

• Neutrophil count < 1500 x106/L

• Platelet count <75,000 x 106/L

• Hemoglobin <10g/dL

• Any disorder (including psychiatric), condition or clinically significant disease (other than a diagnosis of SLE) that would, by it progressive nature and/or severity, interfere with the study evaluation, completion and/or procedures in the medical judgment of the investigator. This includes any age related co-morbidites such as presence of congestive heart failure, angina, chronic obstructive pulmonary disease, asthma, and malignancies (other than resected squamous and basal cell carcinoma of the skin).

• Presence or history of vasculitis (comprising internal organs or extremities or leading to peripheral neuropathy) within the last 3 years, presence or history of active CNS lupus (defined as seizure disorder, cerebral vascular accident, psychosis ascribed to SLE , encephalitis, meningitis, and myelitis) requiring therapy within the last 3 years;

• Uncontrolled hypertension (Blood pressure > 150/95);

• Poorly controlled diabetes (HbA1c > 8%);

• Any history of granulomatous disease including autoimmune granulomatous vasculitis and sarcoidosis;

• Underlying condition that predisposes the subject to infections (eg, history of splenectomy);

• Any disorder or condition that prevents the subject from providing truly informed consent;

• Prior administration of any other biologic that primarily targets the immune system (eg, Lymphostat-B, TACI-Ig, or CTLA4-Ig) in the past 9 months. This includes prior administration of AMG 557;

• Presence of AMG 557 anti-bodies;

• Prior administration of rituximab > 9 months with CD19+ B cells <5/µL;

• Administration of cyclophosphamide (or any other alkylating agent), cyclosporine, tacrolimus, or sirolimus, or > 100 mg/day prednisone or equivalent in the 6 months prior to randomization;

• Participated in an investigational drug trial involving a monoclonal antibody (not targeting the immune system) within 3 months or 5 half-lives, whichever time period is longer, prior to randomization;

• Participated in any another investigational drug or device trial within the previous 30 days or 5 half-lives, whichever time period is longer, prior to randomization;

• Administration of >10 mg/day prednisone (or equivalent) in the 30 days prior to randomization;

• Known sensitivity to mammalian derived products;

• Unwilling to practice an effective method of double-barrier contraception as determined by the investigator for the duration of the study;

• Positive serum hCG at screening or positive urine hCG on D-1; or females who are currently lactating;

• Known allergies to shellfish or any excipients found in KLH;

• Previous immunization with KLH.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Lupus Erythematosus, Systemic
• Systemic Lupus Erythematosus

Intervention

Drug:
• AMG 557
A total of 4 cohorts will be administered multiple doses of drug or placebo subcutaneously. Dose escalation will take place by cohort.

Locations

Country	Name	City	State
Canada	Research Site	Newmarket	Ontario
United States	Research Site	Amarillo	Texas
United States	Research Site	Anniston	Alabama
United States	Research Site	Dallas	Texas
United States	Research Site	Danbury	Connecticut
United States	Research Site	Duncansville	Pennsylvania
United States	Research Site	Manhasset	New York
United States	Research Site	Miami	Florida
United States	Research Site	Michigan City	Indiana
United States	Research Site	Phoenix	Arizona
United States	Research Site	Rochester	New York
United States	Research Site	San Leandro	California

Sponsors (1)

Lead Sponsor	Collaborator
Amgen

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Subject incidence of treatment-emergent adverse events and the incidence of antibodies to AMG 557.		Throughout study period	Yes
Secondary	Serum PK profile of AMG 557 after multiple dose administrations. Biomarkers of pharmacodynamic activity for AMG 557.		Throughout study period	No

External Links

•   AmgenTrials clinical trials website