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Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency Clinical Trials Info presented on Clinical Trials Search isn't intended to be a substitute for certified health advice, travels to or treatment by using a genuine physician. We are not physicians. Always consult your dr. on Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency conditions. Clinical Trials Search.org is a site committed to listing clinical research studies in human subjects. Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency Clinical research trials and Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency health trials occur in hundreds of cities throughout the U.S.A.. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials typically assess the effectivity of new drugs. The propose of the studies / undertakings is to resolve certain human health questions. Clinical trials are a popular means for physicians, government agencies, and private sector companies to locate treatments for all sorts of conditions, including Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency. Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency Clinical Trials and other clinical trials permit volunteers to acquire medical treatment choices before they are available to the masses. Some times the test subjects obtain professional assistance for free, and every now and again they are compensated for their time. Sometimes there is a cost for a Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency clinical trial. Participants oftentimes recieve the most expert healthcare available for their Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency condition. Hazards are a reality, however, and can include extra or frequent physician visits, health risks (potentially life-endangering), and/or the treatment being uneffective. Trials are federally governed with rigorous guidelines to protect clinical trials subjects.

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Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency



Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency

For Condition: Factor IX Deficiency,Hemophilia B
Status: Completed
Sponsor(s): National Center for Research Resources (NCRR) , University of North Carolina
Synopsis: OBJECTIVES: Assess the safety and long-term efficacy of monoclonal factor IX concentrate in patients with factor IX deficiency.
Details: PROTOCOL OUTLINE: Patients receive monoclonal factor IX replacement therapy as inpatients. Patients with a satisfactory response receive further therapy as needed for bleeding for up to 36 months at home.
Eligibility:
Study Type:
  Interventional, Treatment, Safety/Efficacy Study
Minimum Age/Maximum Age: 12 Years/
Genders: Both
Protocol Entry Criteria: PROTOCOL ENTRY CRITERIA: Patients with factor IX deficiency.
Total Enrollment: 3

Location and Contact Information:

Overall Study Official:
GilbertWhite,  Study Chair,  University of North Carolina


Additional Information:
Study ID Numbers:
  199/11956;  UNCCH-621
Study Start Date: March 1992
Record last reviewed: January 1998
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00004801

Other Factor Ix Deficiency Studies:
1. Safety of a New Type of Treatment Called Gene Transfer for the Treatment of Severe Hemophilia B

2. Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency

3. Severe Hemophilia B Study

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