A clinical trial to study the effects of IB1001,in previously treated patients children with Hemophilia B
- Conditions
- Health Condition 1: null- Previously Treated Pediatric Subjects with Hemophilia B State the primary health condition(s) or problem(s) studied
- Registration Number
- CTRI/2011/06/001832
- Lead Sponsor
- Aptevo Bio Therapeutics LLC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 22
1. Subjectâ??s parent or legal guardian must give written Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved informed consent and be willing to make the required study visits and follow instructions while enrolled in the study. For subjects >=7 years of age, assent will be obtained if required by the institution. For subjects < 7 years of age, legal assent is not reasonable to obtain.
2. Severe (factor IX activity <=2 IU/dL) hemophilia B subjects currently on-demand therapy with a minimum of 2 bleeding episodes requiring factor IX therapy over the preceding 6 months or 4 bleeding
episodes over the preceding 12 months; subjects on prophylaxis with a bleeding pattern similar to that above demonstrated prior to starting prophylaxis. In children under 5 years of age, severity may be indicated by the occurrence of one or more joint bleeds at any point in the childâ??s history requiring infusion(s) to replace factor IX.
3. Immunocompetent (CD4 count >400/mm3) and not receiving immune modulating or chemotherapeutic agents
4. Previously treated patients with a minimum of 50 exposure days to a factor IX preparation 8 of 48 Confidential and Proprietary
5. Platelet count at least 150,000/mm3
6. Liver function: alanine transaminase [ALT] and aspartate transaminase [AST] <=2 times the upper limit of the normal range
7. Total bilirubin <=1.5 times the upper limit of the normal range
8. Renal function: serum creatinine <=1.25 times the upper limit of the normal range
9. Willingness to participate in the trial for approximately 6 months (50 exposures)
10. Age <=12 years
11. Hemoglobin >=7 g/dL at the time of the blood draw
1. History of factor IX inhibitor >=0.6 Bethesda units (BU)
2. Existence of another coagulation disorder
3. Evidence of thrombotic disease, fibrinolysis, or disseminated intravascular coagulation (DIC)
4. Use of an investigational drug within 30 days prior to study entry
5. On medications that could impact hemostasis, such as aspirin
6. History of poor compliance, a serious medical or social condition, or any other circumstance that, in the opinion of the investigator, would interfere with participation or compliance with the study protocol
7. History of adverse reaction to either plasma-derived factor IX or recombinant factor IX that interfered with the subjectâ??s ability to treat bleeding episodes with a factor IX product
8. Hypersensitivity to the active substance or to any excipients in the investigational products
9. Known allergic reaction to hamster proteins
10. In Poland children weighing < 17.5 kg will be excluded
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the pharmacokinetics, safety (acute effects associated with infusions, and inhibitor development) and efficacy (breakthrough bleeding and control of hemorrhaging during prophylaxis) of IB1001 in previously treated pediatric subjects with hemophiliaTimepoint: 6 Months
- Secondary Outcome Measures
Name Time Method Safety Assessments <br/ ><br>Investigators and subject/parent/guardian will report AEs that occur anytime during the study <br/ ><br>Timepoint: 6 Months