Phase
Condition
Platelet Disorders
Pregnancy Complications
Antiphospholipid Syndrome
Treatment
Certolizumab Pegol
Clinical Study ID
Ages 18-40 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Pregnant as defined by positive test for elevated ß-HCG and having a live,appropriate sized embryo by ultrasound, but <8 weeks gestation;
Antiphospholipid syndrome (APS);
Positive for LAC on two or more occasions greater than 12 weeks apart within theprevious 18 months. If a candidate for the study is newly diagnosed (<12 weeks) withAPS, meets clinical criteria for APS and has one positive LAC confirmed by review ofthe medical record, she may be consented and screened. At baseline, LAC will bemeasured at the study core lab and she will be enrolled if it is found to bepositive. The LAC measurement will be repeated 12 weeks after the initialdetermination and, if positive, she will remain in the study.
Age 18-40 (+364 days) years of age and able to give informed consent
Laboratory hematocrit >26% at time of screening.
the diagnosis of APS and LAC will be confirmed by one of the Co-PI's for each case by a review of the medical records.
Exclusion
Exclusion Criteria:
Hypertension (BP >140/90) present at screening;
Multifetal gestation;
Type 1 or Type 2 diabetes antedating pregnancy;
SLE patients requiring prednisone >10 mg/day;
Platelet count <100,000 per microliter;
Women currently taking prednisone greater than 10 mg daily for an autoimmunedisorder, other than immune thrombocytopenia; a. More than 60 mg once daily in a tapering regimen or 20 mg once daily in amaintenance regimen for immune thrombocytopenia
Women with urinary excretion with greater than 500 mg (0.5 g) per day (spot urineprotein/creatinine ration 0.5);
Serum creatinine >1.2 mg/dL
History of tuberculosis or untreated positive PPD;
Women with a tuberculin skin test induration of 5 mm or greater; or positivequantiFERON-gold test
Women with HIV, Hepatitis B or Hepatitis C positive status;
Known contraindications or relative contraindications to certolizumab:
Active infection, e.g., chronic hepatitis B
History of recurrent infection, e.g., recurrent cellulitis, or opportunisticinfection
History of prior active/treated endemic mycoses in the last two years (including coccidioidomycosis, blastomycosis, or histoplasmosis)
History of heart failure
History of peripheral demyelinating disease or Guillian-Barre syndrome
History of hematologic malignancy
Prior adverse reaction to certolizumab or o ther anti-TNF-α agent
Study Design
Study Description
Connect with a study center
TRIO Advancing Reproductive Care
Toronto, Ontario M5G 2K4
CanadaActive - Recruiting
Hospital for Special Surgery
New York, New York 10021
United StatesActive - Recruiting
University of Utah
Salt Lake City, Utah 84132
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.