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Hemophilia BPhase 3NCT01174446

Pivotal Study (Pharmacokinetics, Efficacy, Safety) of BAX 326 (rFIX) in Hemophilia B Patients

A Phase 3 study testing BAX 326 and BeneFIX in people with Hemophilia B, run by Baxalta now part of Shire at 25 sites in 14 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this pivotal Phase 1/3 study is to determine the pharmacokinetic (PK) parameters, the hemostatic efficacy, and the safety of BAX 326, a recombinant factor IX, in previously treated patients (PTPs) with severe and moderately severe hemophilia B. Read more about this study

Who is it for?
Ages 12 to 65 years
Conditions the study is for
Hemophilia B
What is being tested?
BAX 326 and BeneFIX
Could I receive a placebo?
No, everyone receives an active treatment
How many people
86 participants
Where
25 sitesin 14 countries
Study dates
29 Jul 2010to 3 May 2012
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 65 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Main Inclusion Criteria:

  • Participant is 12 to 65 years old at the time of screening
  • Participant and/or legal representative has/have provided signed informed consent
  • Participant has severe (factor IX (FIX) level < 1%) or moderately severe (FIX level 1-2%) hemophilia B (based on the one stage activated partial thromboplastin time (aPTT) assay), as tested at screening at the central laboratory
  • Participant is previously treated with plasma-derived or recombinant FIX concentrate(s) for a minimum of 150 exposure days (EDs) (based on the participant's medical records); if a verifiable, documented history is unavailable, the participant can be enrolled if s/he has 100-150 EDs to any FIX product that are not fully documented and has participated in Study 050901 for at least 50 EDs to Immunine prior to enrollment (not valid for US and Japan).
  • Participant has no evidence of a history of FIX inhibitors
  • If the participant is to receive prophylactic treatment, the participant is willing to receive prophylactic treatment over a period of 6 months.
  • If the participant is to receive on-demand treatment, the participant has ≥12 documented bleeding episodes requiring treatment within 12 months prior to enrollment and is willing to receive on-demand treatment for the duration of this study.

Main Exclusion Criteria:

  • The participant has a history of FIX inhibitors with a titer ≥0.6 Bethesda Units (BU) (as determined by the Nijmegen modification of the Bethesda assay or the assay employed in the respective local laboratory) at any time prior to screening
  • The participant has a detectable FIX inhibitor at screening, with a titer ≥0.6 BU as determined by the Nijmegen modification of the Bethesda assay in the central laboratory
  • The participant's weight is < 35 kg or > 120 kg
  • The participant has a history of allergic reaction, eg, anaphylaxis, following exposure to FIX concentrate(s)
  • The participant has a known hypersensitivity to hamster proteins or recombinant furin (rFurin)
  • The participant has ongoing or recent evidence of a thrombotic disease, fibrinolysis or disseminated intravascular coagulation (DIC)

Trial locations and contacts

25 sites in 14 countries.

25 sites in 14 countries

Japan4 sites
  • Study site

    Hiroshima

  • Study site

    Nara

  • Study site

    Tochigi

  • Study site

    Tokyo

Other trials in Japan

Poland4 sites
  • Study site

    Gdansk

  • Study site

    Krakow

  • Study site

    Lodz

  • Study site

    Warsaw

Other trials in Poland

Russia3 sites
  • Study site

    Kirov

  • Study site

    Moscow

  • Study site

    Saint Petersburg

Other trials in Russia

Brazil2 sites
  • Study site

    Brasília

  • Study site

    São Paulo

Other trials in Brazil

Colombia2 sites
  • Study site

    Bogotá

  • Study site

    Cali

Other trials in Colombia

Romania2 sites
  • Study site

    Bucharest

  • Study site

    Timișoara

Other trials in Romania

Argentina1 site
  • Study site

    Rosario

Other trials in Argentina

Bulgaria1 site
  • Study site

    Sofia

Other trials in Bulgaria

Chile1 site
  • Study site

    Santiago

Other trials in Chile

Czechia1 site
  • Study site

    Prague

Other trials in Czechia

Spain1 site
  • Study site

    Barcelona

Other trials in Spain

Sweden1 site
  • Study site

    Malmö

Other trials in Sweden

Ukraine1 site
  • Study site

    Lviv

Other trials in Ukraine

United Kingdom1 site
  • Study site

    London

Other trials in United Kingdom

About this study

Official title: Recombinant Factor IX (BAX 326): A Phase 1/3, Prospective, Controlled, Multicenter Study Evaluating Pharmacokinetics, Efficacy, Safety and Immunogenicity in Previously Treated Patients With Severe or Moderately Severe Hemophilia B

The purpose of this pivotal Phase 1/3 study is to determine the pharmacokinetic (PK) parameters, the hemostatic efficacy, and the safety of BAX 326, a recombinant factor IX, in previously treated patients (PTPs) with severe and moderately severe hemophilia B.

Conditions
Hemophilia B
Being tested
BAX 326, BeneFIX
Medical subject headings
Hemophilia B

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BAX 326Biological

    Also called Recombinant factor IX (rFIX), RIXUBIS

    • Study Part 1: Pharmacokinetic (PK) Crossover with BAX326 and BeneFIX
    • Study Part 2: Open-label evaluation of prophylaxis and on-demand BAX326 only
    • Study Part 3: Open-label repeat of PK evaluation (repeat Study Part 1) with BAX326 only and same study participants as Study Part 1
  • BeneFIXBiological

    Also called Recombinant factor IX (rFIX)

    • Study Part 1: Pharmacokinetic (PK) Crossover with BAX326 and BeneFIX.
    • BeneFIX only used in Part 1 of this study.
    • Study Part 2 and 3 only utilized BAX326
Study groups in NCT01174446
Study groupRoleWhat they receive
BAX 326ExperimentalRecombinant factor IX (rFIX)
Receives: Biological: BAX 326
BeneFIXActive comparatorRecombinant Factor IX (rFIX)
Receives: Biological: BeneFIX

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Study Part 1- Area Under the Plasma Concentration Versus Time Curve From 0 to 72 Hours Per Dose

    Computed using the linear trapezoidal method. The concentration at 72 hours was interpolated from the two nearest sampling time points or extrapolated using the last quantifiable concentration and the terminal rate constant λz. λz was estimated from the slope of natural log-linear fitting to latter quantifiable concentrations, with largest adjusted R^2.

    Measured: 72 hours

Secondary outcomes (49)
  1. Study Parts 1 and 3: Area Under the Plasma Concentration/Time Curve From Time 0 to Infinity Per Dose (AUC0-∞/ Dose)

    Defined as (AUC0-t + Ct)/ λz/ dose, where t is the time of last quantifiable concentration, Ct is the last quantifiable concentration. λz will be estimated from the slope of natural log-linear fitting to latter quantifiable concentrations, with largest adjusted R^2. The objective of Study Part 3 was to re-evaluate the Pharmacokinetic (PK) parameters for BAX 326 after a period of 6 months of treatment, in participants who accumulated at least 30 EDs to BAX 326, and to compare them with those determined in the same participants participating in Study Part 1.

    Measured: 0-30 minutes before infusion up to 72 hours post-infusion

  2. Study Parts 1 and 3: Mean Residence Time (MRT)

    Computed as Area under the moment curve 0-∞ (AUMC0-∞) / AUC0-∞- TI/2, where AUMC0-∞ will be determined in a similar manner as AUC0-∞ and TI represents infusion duration [hr] The objective of Study Part 3 was to re-evaluate the Pharmacokinetic (PK) parameters for BAX 326 after a period of 6 months of treatment, in participants who accumulated at least 30 EDs to BAX 326, and to compare them with those determined in the same participants participating in Study Part 1.

    Measured: 0-30 minutes before infusion up to 72 hours post-infusion

  3. Study Parts 1 and 3: Clearance (CL)

    Computed as Dose/ AUC0-∞. The objective of Study Part 3 was to re-evaluate the Pharmacokinetic (PK) parameters for BAX 326 after a period of 6 months of treatment, in participants who accumulated at least 30 EDs to BAX 326, and to compare them with those determined in the same participants participating in Study Part 1.

    Measured: 0-30 minutes before infusion up to 72 hours post-infusion

  4. Study Parts 1 and 3: Incremental Recovery at Cmax (IR at Cmax)

    Defined as (Cmax - Cpre-infusion)/Dose, where maximum concentration (Cmax) will be determined as the highest concentration achieved within one hour after infusion. The objective of Study Part 3 was to re-evaluate the Pharmacokinetic (PK) parameters for BAX 326 after a period of 6 months of treatment, in participants who accumulated at least 30 EDs to BAX 326, and to compare them with those determined in the same participants participating in Study Part 1.

    Measured: 0-30 minutes before infusion up to 1 hour post-infusion

  5. Incremental Recovery (IR) at 30 Minutes Over Time

    IR at 30 Minutes was measured at the following time points during the study: - Part 1 or Part 2, Exposure Day (ED) 1. (If participant was present for Study Part 1, then ED 1 from Part 1 was used. If Participant entered study in Study Part 2, then ED 1 from Part 2 was used.) - Part 2: Week 5 - Part 2: Week 13 - Part 2 or Part 3: Week 26 (Week 26 of study participation) - Study Completion or Termination Visit

    Measured: 0-30 minutes before infusion and 30 minutes post-infusion

  6. Change in Incremental Recovery (IR) at 30 Minutes Over Time

    The median changes in IR at 30 Minutes, calculated as the change in IR value from exposure day 1 (ED1).

    Measured: 0-30 minutes before infusion and 30 minutes post-infusion

  7. Study Parts 1 and 3: Half Life (T 1/2)

    Elimination phase half-life will be determined as ln2/ λz. The objective of Study Part 3 was to re-evaluate the Pharmacokinetic (PK) parameters for BAX 326 after a period of 6 months of treatment, in participants who accumulated at least 30 EDs to BAX 326, and to compare them with those determined in the same participants participating in Study Part 1.

    Measured: 0-30 minutes before infusion up to 72 hours post-infusion

  8. Study Parts 1 and 3: Volume of Distribution at Steady State (Vss)

    Vss computed as CL·MRT. The objective of Study Part 3 was to re-evaluate the Pharmacokinetic (PK) parameters for BAX 326 after a period of 6 months of treatment, in participants who accumulated at least 30 EDs to BAX 326, and to compare them with those determined in the same participants participating in Study Part 1.

    Measured: 0-30 minutes before infusion up to 72 hours post-infusion

  9. Study Part 2: Annualized Bleed Rate (ABR) During Treatment With BAX326

    ABR during prophylaxis (twice-weekly) in Part 2 was calculated as (Number of bleeding episodes/observed treatment period in days) * 365.25. The treatment period on prophylaxis was defined as time between the first and the last prophylactic infusions and ABR on prophylaxis was calculated for participants who received a minimum of 3 months of prophylactic treatment with BAX326.

    Measured: Study Part 2 = 26 weeks ± 1 week (Note: Study Part 1 = 2-4 weeks)

  10. Bleeding Episodes Treated With 1, 2 or ≥3 Infusions of BAX326 by Bleeding Site and Cause

    The number of bleeding episodes treated with 1, 2, or ≥3 infusions of BAX326 to achieve adequate hemostasis. Only infusions required until resolution of bleed were considered.

    Measured: Study Part 2 = 26 weeks ± 1 week (Study Part 2 began at week 3-5)

  11. Hemostatic Efficacy at Resolution of All Bleeding Episodes (BEs) Treated With BAX326 by Bleeding Site and Cause

    Rating Scale for Treatment of BEs (4-point ordinal scale): -Excellent: Full relief of pain and cessation of objective signs of bleeding (eg, swelling, tenderness, and decreased range of motion in the case of musculoskeletal hemorrhage) after a single infusion. No additional infusion required for the control of bleeding. Administration of further infusions to maintain hemostasis did not affect this scoring. -Good: Definite pain relief and/or improvement in signs of bleeding after a single infusion. Possibly requires more than 1 infusion for complete resolution. -Fair: Probable and/or slight relief of pain and slight improvement in signs of bleeding after single infusion. Required more than 1 infusion for complete resolution. -None: No improvement or condition worsens.

    Measured: At bleed resolution throughout the study period of 22 months (Study Parts 1, 2, and 3)

  12. Total Weight-adjusted Dose Per Bleeding Episode (BEs) of All BEs Treated With BAX326 by Bleeding Site and Cause

    Measured: Study Part 2 = 26 weeks ± 1 week (Note: Study Part 1 = 2-4 weeks)

  13. Consumption of BAX326 Per Event Per Participant

    Weight-adjusted consumption of BAX326 by event per participant, i.e., for prophylactic treatment and for treatment of bleeds until resolution of bleed.

    Measured: Study Part 2 = 26 weeks ± 1 week (Note: Study Part 1 = 2-4 weeks)

  14. Consumption of BAX326 Per Participant: Median Number of Infusions Per Month

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week (Prophylaxis and On-Demand period), Study Part 3 = 1 week (Total = 29-31 weeks)

  15. Consumption of BAX326 Per Participant: Median Weight-adjusted Consumption Per Month

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week (Prophylaxis and On-Demand period), Study Part 3 = 1 week (Total = 29-31 weeks)

  16. Number of Participants Who Developed Inhibitory Antibodies to Factor IX (FIX)

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  17. Occurrence of Total Binding Antibodies of Indeterminate Specificity (Within Assay Variability)

    Occurrence of total binding antibodies of indeterminate specificity (within assay variability) to FIX, antibodies to CHO proteins and rFurin is defined by a dilution of 2 or less increase as compared to levels at screening visit (e.g. negative to 1:20 or 1:40).

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  18. Occurrence of Treatment Related Total Binding Antibodies

    Occurrence of treatment related total binding antibodies to Factor IX (FIX), antibodies to Chinese hamster ovary (CHO) proteins, and recombinant furin (rFurin) is defined by more than 2-dilution increase as compared to levels at screening visit and confirmed specificity (e.g. negative to 1:80)

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  19. Number of Participants Who Experienced Severe Allergic Reactions (e.g. Anaphylaxis)

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  20. Number of Participants Who Experienced Thrombotic Events

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  21. Number of Participants With Clinically Significant Changes in Laboratory Parameters: Clinical Chemistry

    Clinically significant changes in chemistry assessments for Alanine Aminotransferase, Albumin, Alkaline Phosphatase, Aspartate Aminotransferase, Bicarbonate, Bilirubin, Blood Urea Nitrogen, Chloride, Glucose, Potassium, Protein (Serum), Sodium. Clinically Significant (CS) defined as: -1. The abnormal value constitutes an adverse event (AE) and, -2. The abnormal value is a symptom of or related to a disease that is already recorded as an AE in Case Report Form (CRF).

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  22. Number of Participants With Clinically Significant Changes in Laboratory Parameters: Hematology

    Clinically significant changes in hematology assessments for Basophils, Basophils/Leukocytes, Eosinophils, Eosinophils/Leukocytes, Erythrocyte Mean Corpuscular Hemoglobin Concentration, Erythrocyte Mean Corpuscular Volume, Erythrocytes, Hematocrit, Hemoglobin, Leukocytes, Lymphocytes, Lymphocytes/Leukocytes, Monocytes, Monocytes/Leukocytes, Neutrophils, Neutrophils/Leukocytes, Platelets,

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  23. Number of Participants With Clinically Significant Changes in Laboratory Parameters: Vital Signs

    Clinically significant changes in vital signs assessments for pulse rate, systolic/diastolic blood pressure, respiratory rate, body temperature

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  24. Number of Participants With Clinically Significant Changes in Laboratory Parameters: Thrombogenic Markers

    Clinically significant changes in thrombogenic markers assessments for thrombin-antithrombin (TAT), prothrombin fragment 1.2, and D-dimer as evaluated by an independent Data Monitoring Committee (DMC)

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  25. Number of Adverse Events (AEs) After BAX326 Treatment

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, and Study Part 3 = 1 week (Total = 29-31 weeks)

  26. Number of Participants With Adverse Events (AEs) After BAX326 Treatment

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, and Study Part 3 = 1 week (Total = 29-31 weeks)

  27. EuroQoL (Quality of Life)-5 Dimensions (EQ-5D) Total Index Scores

    EQ-5D is a participant answered questionnaire scoring 5 dimensions - mobility, self-care, usual activities, pain/discomfort and anxiety/depression. The EQ-5D total score ranges from 0 (worst health state) to 1 (perfect health state) and 1 reflects the best outcome.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  28. EuroQoL (Quality of Life)-5 Dimensions Visual Analogue Scale (EQ-5D VAS) Scores

    Participant rated questionnaire to assess health-related quality of life in terms of a single index value. The VAS component rates current health state on a scale from 0 (worst imaginable health state) to 100 (best imaginable health state); higher scores indicate a better quality of life.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  29. General Pain Assessment Through a Visual Analog Scale (VAS)

    Participant rated assessment of health-related quality of life. The VAS Pain Scale rates current health state on a scale from 0 (no pain) to 100 (worst imaginable pain). For the pain scale, a higher score indicates worse pain.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  30. Short Form (36) Health Survey (SF-36): HRQoL 'Physical Component Score' (PCS)

    The PCS is a summary scale of the dimensions physical functioning, role physical, bodily pain, and general health. The component score is normalized to a standard population. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  31. SF-36: HRQoL 'Mental Health' (MH)

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  32. SF-36: HRQoL Physical Functioning' (PF)

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  33. SF-36: HRQoL Role-Physical (RP)

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  34. SF-36: HRQoL Role-Emotional

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  35. SF-36: HRQoL Bodily Pain

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  36. SF-36: HRQoL Mental Health

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  37. SF-36: HRQoL Vitality

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  38. SF-36: HRQoL Social Functioning

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  39. SF-36: HRQoL General Health

    Quality of life survey response as measured using the SF-36 questionnaire. Scores range from 0 to 100 with higher scores representing better health. There is no total overall score; scoring is done for both subscores and summary scores. The raw data from the SF-36 items were transformed to norm based scores for each of the 8 HRQoL/SF-36 health domain scores.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  40. Pediatric Quality of Life Questionnaire (PedsQL) Physical Health Summary Score (Ages 12-16)

    The Peds-QL is a generic Health-Related Quality of Life (HR QoL) instrument designed specifically for a pediatric population. It captures the following domains: general health/activities, feelings/emotional, social functioning, school functioning. For this study, the Peds-QL for 12 to 16-year-old subjects was used. Higher scores indicate better quality of life (QOL) for all domains of the Peds-QL. This modular instrument uses a 5-point scale: from 0 (never) to 4 (almost always). Items are reversed scored and linearly transformed to a 0-100 scale as follows: 0=100, 1=75, 2=50, 3=25, 4=0. 4 dimensions (physical, emotional, social, \& school functioning) are scored.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  41. Pediatric Quality of Life Questionnaire (PedsQL) Psychosocial Health Summary Score (Ages 12-16)

    The Peds-QL is a generic Health-Related Quality of Life (HR QoL) instrument designed specifically for a pediatric population. It captures the following domains: general health/activities, feelings/emotional, social functioning, school functioning. For this study, the Peds-QL for 12 to 16-year-old subjects was used. Higher scores indicate better quality of life (QOL) for all domains of the Peds-QL. This modular instrument uses a 5-point scale: from 0 (never) to 4 (almost always). Items are reversed scored and linearly transformed to a 0-100 scale as follows: 0=100, 1=75, 2=50, 3=25, 4=0. 4 dimensions (physical, emotional, social, \& school functioning) are scored.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  42. Pediatric Quality of Life Questionnaire (PedsQL) Total Score (Ages 12-16)

    The Peds-QL is a generic Health-Related Quality of Life (HR QoL) instrument designed specifically for a pediatric population. It captures the following domains: general health/activities, feelings/emotional, social functioning, school functioning. For this study, the Peds-QL for 12 to 16-year-old subjects was used. Higher scores indicate better quality of life (QOL) for all domains of the Peds-QL. This modular instrument uses a 5-point scale: from 0 (never) to 4 (almost always). Items are reversed scored and linearly transformed to a 0-100 scale as follows: 0=100, 1=75, 2=50, 3=25, 4=0. 4 dimensions (physical, emotional, social, \& school functioning) are scored.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  43. Health-Related Quality of Life (HRQoL) Disease-specific: Haem-A-QoL

    The Haem-A-QOL instrument has been developed and used in hemophilia A patients. As a hemophilia-specific instrument, this measure assesses very specific aspects of dealing with hemophilia. The areas covered by this instrument are: physical health, sports/leisure, school/work, dealing with hemophilia, and outlook for the future. For the Haem-A-QOL, higher scores indicate a worse quality of life. Scores on a scale range between 0 and 100.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  44. Health-Related Quality of Life (HRQoL) Disease-specific: Haemo-QoL - Participants On-Demand (Ages 12-16)

    The Haemo-QoL is a quality of life (QoL) assessment instrument for children and adolescents with haemophilia. As a hemophilia-specific instrument, this measure assesses very specific aspects of dealing with hemophilia. For the Haemo-QoL, higher scores indicate a worse quality of life. Scores on a scale range between 0 and 100.

    Measured: Baseline at either Study Part 1, or Study Part 2, and End of Study (study weeks 29-31)

  45. Health Resource Use - Number of Hospitalizations

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  46. Health Resource Use - Total Days of Hospital Stay

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  47. Health Resource Use - Emergency Room Visits

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  48. Health Resource Use - Unscheduled Doctor's Office Visits

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

  49. Health Resource Use - Days Lost From Work or School

    Measured: Study Part 1 = 2-4 weeks, Study Part 2 = 26 weeks ± 1 week, Study Part 3 = 1 week (Total = 29-31 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Aug 2010 (estimated)
  2. Study start29 Jul 2010
  3. Primary completion3 May 2012
  4. Study completion3 May 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
86 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01174446
Sponsor's protocol ID
250901
Other IDs
2009-016720-31, 2009
Status last verified
Apr 2021
First submitted
2 Aug 2010
Last updated
20 May 2021
Data monitoring committee
Yes

Publications

  • Windyga J, Lissitchkov T, Stasyshyn O, Mamonov V, Rusen L, Lamas JL, Oh MS, Chapman M, Fritsch S, Pavlova BG, Wong WY, Abbuehl BE. Pharmacokinetics, efficacy and safety of BAX326, a novel recombinant factor IX: a prospective, controlled, multicentre phase I/III study in previously treated patients with severe (FIX level <1%) or moderately severe (FIX level </=2%) haemophilia B. Haemophilia. 2014 Jan;20(1):15-24. doi: 10.1111/hae.12228. Epub 2013 Jul 9.

    PubMed 23834666

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing BAX 326 and BeneFIX in people with Hemophilia B, run by Baxalta now part of Shire at 25 sites in 14 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 May 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 25 sites in Japan, Poland, Russia, Brazil, Colombia and 9 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 25 Nov 2013). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Study Part 1- Area Under the Plasma Concentration Versus Time Curve From 0 to 72 Hours Per Dose (time frame: 72 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01174446, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 May 2021.

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