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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 is not intended to be a substitute for certified medical advice, visits or professional assistance using a real physician. We are not physicians. Always consult your dr. about Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency conditions. Clinical Trials Search.org is a site dedicated 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 happen in many of localities throughout the U.S.. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials typically measure the effectualness of new drugs. The function of the studies / projects is to resolve particular human medical questions. Clinical trials are a popular manner for mDs, government agencies, and private sector corporations to discover remedies for all varieties of circumstances, like 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 allow volunteers to obtain healthcare treatment options before they are available to the masses. Some times the participants undergo professional assistance for free of charge, and occasionally they are paid 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. Human subjects often get the best healthcare available for their Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency condition. Dangers are a reality, however, and may include additional or frequent mD visits, healthcare dangers (potentially life-jeopardising), and/or the treatment being ineffectual. Trials are federally governed with rigorous guidelines to protect clinical trials patients.

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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

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