Skip to main content
OpenTrials
Completed

NCT Number: NCT01878123

Study to Assess the Safety, Tolerability, and Pharmacokinetics of AMP-110 in Subjects With Rheumatoid Arthritis

This is a Phase 1, single-dose, placebo-controlled, dose-escalation,multi-center, first time in human study of AMP-110 in adult subjects with rheumatoid arthritis.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Pinnacle Research Group, LLC, Anniston, Alabama, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be able to provide written informed consent
  • Body mass index 18.5 to 35.0 kg/m2
  • Diagnosis of Rheumatoid Arthritis according to 1987 revised American College of Rheumatology (ACR) criteria
  • Global Functional Class I, II, or III according to ACR 1991 revised criteria
  • Stable use of >/= 1 Disease Modifying Anti-rheumatic Drugs (DMARD) for >/= 4 weeks prior to Day 0, including:
  • Methotrexate (MTX) 7.5 - 25 mg/week
  • Hydroxychloroquine (HCQ) </= 400 mg/day
  • Sulfasalazine (SSZ) 1,000 - 3,000 mg/day
  • Leflunomide 5 - 20 mg/day
  • Azathioprine 150 mg/day or 2 mg/kg/day
  • Combinations of MTX, HCQ, and/or SSZ allowed

Exclusion criteria

  • Prior to Day 0, use of
  • Abatacept
  • Rituximab within 6 months
  • Infliximab, Adalimumab, Certolizumab, Tocilizumab, Cyclosporine, or Mycophenolate mofetil within 2 months
  • Etanercept or Anakinra within 28 days
  • Immunoglobulin or blood products within 28 days
  • Evidence of any active or recent infection including ongoing, chronic infectious disease such as chronic renal infection or chronic chest infection with bronchiectasis or sinusitis
  • History of systemic autoimmune disease other than Rheumatoid Arthritis
  • History of allergic reactions to other protein therapeutics such as monoclonal antibodies or fusion proteins
  • History of anaphylaxis or allergic diathesis
  • Clinically significant cardiac disease, including: unstable angina; myocardial infarction within 6 months; congestive heart failure; arrhythmia requiring active therapy, with the exception of clinically insignificant extrasystoles, or minor conduction abnormalities; and history of clinically significant abnormality on electrocardiogram
  • Evidence of active or latent tuberculosis
  • Vaccination wtih live attenuated viruses within the 2 weeks prior to Day 0
  • Evidence of infection with hepatitis B virus, hepatitis C virus, human immunodeficiency virus 1 or 2, or active infection with hepatitis A
  • Pregnant or breastfeeding women

Treatment and study plan

AMP-110

Biological

Dose levels 1 through 7: Single intravenous infusion on Day 0

Placebo

Other

Dose levels 4 through 7: Single intravenous infusion on Day 0

Primary outcomes

  1. Evaluate the safety and tolerability of a single dose of AMP-110 versus placebo

    Time frame: From start of study drug administration through Day 56

    Evaluate number of subjects with dose-limiting toxicities (through Day 14), evaluate number of subjects wtih adverse events (through Day 56), and number of subjects wtih changes from baseline in laboratory values, vital signs, physical exam and electrocardiogram (through Day 56)

  2. Determine Maximum Tolerated Dose and/or recommended dose level(s) for future clinical trials

    Time frame: From start of study drug administration through Day 56

    Based on the occurrence of dose-limiting toxicities (through Day 14)

Secondary outcomes

  1. Evaluate pharmacokinetic profile of a single dose of AMP-110

    Time frame: From Day 0 pre-dose through Day 28

    Pharmacokinetics evaluated by area under the serum concentration versus time curve (AUC), peak serum concentration (Cmax), and clearance (Cl) of AMP-110

Other outcomes

  1. Assess pharmacokinetic and pharmacodynamic relationships

    Time frame: From Day 0 pre-dose through Day 56

    Determine if pharmacodynamics effects of AMP-110 on certain cytokine levels and T cell subsets are dependent on serum drug concentrations

  2. Evaluate exploratory biomarkers

    Time frame: From start of study drug administration through Day 56

    Blood samples will be analyzed throughout the study to characterize the physiological effects of AMP-110 treatment and to determine markers that correlate with response to treatment

Sponsors and collaborators

Lead sponsor

MedImmune LLC

Industry

Collaborators

  • Daiichi Sankyo Co., Ltd.

Registry information

Official study title

A Randomized, Single-Dose, Placebo-Controlled, Study of the Safety, Tolerability, and Pharmacokinetics of AMP-110 in Subjects With Rheumatoid Arthritis

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Jun 14, 2013
Registry last updated
Sep 30, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.