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OpenTrials
Completed

NCT Number: NCT01284322

Fresolimumab In Systemic Sclerosis

The purpose of this study is to determine if fresolimumab is safe in treating people with systemic sclerosis (scleroderma) and to investigate the effect of fresolimumab in the skin of these individuals.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Boston University School of Medicine; Rheumatology/Arthritis Center

Boston, Massachusetts, 02118, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Meet ACR criteria for diffuse systemic sclerosis
  • < 24 months since onset of first SSc manifestation other than Raynaud's phenomenon
  • Modified Rodnan Skin Score ≥ 15
  • Male or female adult ( ≥ 18 years of age)
  • Able and willing to give written informed consent and comply with study protocol

Exclusion criteria

  • Moderate or severe pulmonary disease w/ FVC < 80% or DLCO < 70% or ground glass and fibrosis > 20% of lung fields by HRCT
  • Treatment with investigational drug within 4 weeks of screening
  • Ongoing use of high dose steroids (> 10mg/day) or unstable steroid dose in past 4 weeks
  • Treatment with immunosuppressive, cytotoxic, or antifibrotic drug within 4 weeks of screening
  • Positive for HIV, HBV, and/or HCV
  • Known active infection (bacterial, viral, fungal, mycobacterial, or other); not including fungal infection of nail beds or any major infection requiring hospitalization or treatment with IV antibiotics within 4 weeks of screening
  • Patients w/ history of malignancy or premalignant lesion
  • History of keratoacanthoma or squamous cell carcinoma
  • Moderate to severe hepatic impairment
  • SSc renal crisis within 6 months or creatinine > 2.0
  • Lack of IV access for medication administration
  • Moderate or severe cardiac disease with significant arrhythmia, heart failure, or unstable angina
  • Anemia (Hb < 8.5 gm/dL)
  • Thrombocytopenia or blood clotting disorder
  • Patients with organ transplant (including allogeneic bone marrow transplant)

Treatment and study plan

Fresolimumab

Drug

intravenous fresolimumab 1mg/kg, first 8 patients; 5 mg/kg following 8 patients

Other names: GC1008, anti-TGF-beta

Primary outcomes

  1. To evaluate safety of fresolimumab in patients with scleroderma

    Time frame: 24 weeks

  2. To investigate the effect of fresolimumab on TGF-beta responsive gene expression in skin after treatment with fresolimumab compared to pre-treatment TGF-beta responsive gene expression.

    Time frame: 7 weeks

    TGF-beta regulated skin gene expression

Sponsors and collaborators

Lead sponsor

Boston University

Other

Registry information

Official study title

OPEN LABEL TRIAL OF ANTI-TGF-BETA MAB, FRESOLIMUMAB, IN SYSTEMIC SCLEROSIS - A PHASE ONE BIOMARKER TRIAL

Important dates

Study start
2011
Primary completion
2013
Study completion
2014
First posted
Jan 27, 2011
Registry last updated
Jul 16, 2014

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.

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