PLASMA 2 Trial: Examination of Once Daily (QD) Dosing of A-002 In Subjects With Stable Coronary Artery Disease

Completed · Phase 2

Conditions studied: Coronary Artery Disease

In brief

The study will be conducted at up to 25 U.S. centers and will be a double-blind randomized parallel group placebo controlled study among subjects with stable coronary artery disease (CAD). Subjects will be randomized to receive either placebo tablets or one of 2 orally active doses of A-002. The duration of study drug therapy will be 8 weeks.

Key facts

Study ID

NCT00525954

Run by

Anthera Pharmaceuticals

People needed

120

Starts

2007-09-01

Expected to finish

2007-12-01

Last updated by the study team

2008-01-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects are eligible for inclusion if they meet the following inclusion criteria:
• Men and women ≥18 years of age
• Written informed consent from the subject
• Stable CAD
• Stable medical condition, will be compliant and able to comply with the requirements of the protocol

You may not qualify if…

• Subjects must NOT meet any of the following exclusion criteria:
• Planned coronary artery bypass surgery (CABG)
• Acute or chronic heart failure as defined by the New York Heart Association (NYHA) classification as functional Class III or Class IV
• Hospitalization for acute coronary syndrome (ACS) if troponin >0.1 ng/mL in the preceding 6 weeks
• Hospitalization for ST-segment elevation acute myocardial infarction (STEMI) in the preceding 12 weeks
• Subjects with chronic inflammatory disease (e.g., rheumatoid arthritis), inflammatory bowel disease, recent (12 weeks) systemic or localized infection (the latter requiring clinical intervention), or major surgery
• hs-CRP ≥15 mg/L repeated on at least 2 occasions >24 hours apart due to non-cardiovascular systemic inflammatory conditions (e.g., rheumatoid disease)
• Subjects enrolled in another experimental (interventional) protocol within the past 30 days prior to Screening or prior experience with A-002.
• Subjects treated for cancer within the previous 5 years except for skin basal cell carcinoma or carcinoma in situ of the cervix, with measures other than a minor, complete surgical excision (e.g., chemotherapy), or radiation therapy
• Subjects who have received immunosuppressant therapy within 30 days prior to entry
• Subjects who have received anti-tumor necrosis factor (for example, infliximab) therapy within 6 months prior to entry
• The presence of severe liver disease with cirrhosis, recent active hepatitis, active chronic hepatitis, ALT or AST >3 x upper limit of normal, biliary obstruction with hyperbilirubinemia (total bilirubin >2 x upper limit of normal)
• Active cholecystitis, gall bladder symptoms, or potential hepato-biliary abnormalities
• The presence of moderate or severe renal impairment (CrCl <60 mL/min or creatinine >1.5 x upper limit of normal), nephrotic syndrome, or subjects undergoing dialysis
• Uncontrolled diabetes mellitus (known HbA1c >11% within the last 1 month prior to screening)
• Females who are nursing, pregnant, or intend to become pregnant during the time of the study, or subjects who have a positive serum pregnancy test at Visit 1 (if the subject is a female of child-bearing potential). Women of child-bearing potential must also use a reliable method of birth control during the study and for 1 month following completion of therapy. A reliable method for this study is defined as one of the following: oral or injectable contraceptives, intrauterine device (IUD), contraceptive implants, tubal ligation, hysterectomy, a double-barrier method (diaphragm with spermicidal foam or jelly, or a condom).
• Subjects who have a history of alcohol or drug abuse within 1 year of study entry
• Subject living too far from participating center or unable to return for follow-up visits
• Subjects who in the opinion of the Investigator are a poor medical or psychiatric risk for therapy with an investigational drug, are unreliable, or have an incomplete understanding of the study which may affect their ability to take drugs as prescribed or comply with instructions
• Known human immunodeficiency virus (HIV), Hepatitis B virus (HBV), or Hepatitis C Virus (HCV) infection
• Treatment with any systemic corticosteroid within the 30-day period prior to study entry or the use of inhaled steroids within the 14-day period prior to study entry

Where it is running

• Mobile Heart Specialists — Mobile, Alabama, United States
• Sonoran Health Specialists — Scottsdale, Arizona, United States
• Pasco Cardiology Center — Hudson, Florida, United States
• Charlotte Cardiovascular Institute — Port Charlotte, Florida, United States
• Florida Cardiovascular Research Institute — Tampa, Florida, United States
• Augusta Cardiology Clinic — Augusta, Georgia, United States
• Louisville Cardiology Medical Group — Louisville, Kentucky, United States
• Maine Research Associates — Auburn, Maine, United States
• United Medical Associates — Binghamton, New York, United States
• Cardiology PC — Syracuse, New York, United States
• Austin Heart — Austin, Texas, United States
• Clinical Research Associates of Tidewater — Norfolk, Virginia, United States
• Wisconsin Heart, SC — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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