Mode
Text Size
Log in / Sign up
Phase 2 N=23 Treatment

Rituximab to Treat Severe Hemophilia A

Hemophilia A

Enrolled (actual)
23
Serious AEs
68.8%
Results posted
Jun 2013
Primary outcome: Primary: Proportion of Subjects With Major Response, i.e. Inhibitor Level Falls to Less Than 5 BU/mL Between Weeks 6 to 22 and Remains Below 5 BU/mL at 5-7 Days Following Re-challenge With FVIII — .1875 proportion of participants — p=0.043

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Rituximab (Drug)
Age
Pediatric, Adult, Older Adult · 0+ yrs
Sex
All
Sponsor
Carelon Research
Primary completion
Nov 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Proportion of Subjects With Major Response, i.e. Inhibitor Level Falls to Less Than 5 BU/mL Between Weeks 6 to 22 and Remains Below 5 BU/mL at 5-7 Days Following Re-challenge With FVIII
.1875 0.043 sig
SECONDARY
Proportion of Subjects With at Least Minor Response, i.e. Inhibitor Level Falls to <5 BU/mL Between Weeks 6-22 and Either Remains <5 BU/mL 5-7 Days Following FVIII Rechallenge or Titer Following FVIII Rechallenge is 5-10 BU/mL & <50% of Original Peak
0.25
SECONDARY
Percent Change in Inhibitor Titer on Challenge With Factor VIII From Baseline Challenge to Post-treatment Challenge
-64.31
SECONDARY
Median Number of Bleeding Events Per Subject Meeting the Criteria of a Serious Adverse Event
SECONDARY
Median Number of Bleeding Events Per Subject Not Meeting the Criteria of a Serious Adverse Event
19.5
SECONDARY
Median Number of Serious Adverse Events Per Subject Other Than Bleeding Events
1
SECONDARY
Median Number of Adverse Events Per Subject That Were Not Bleeding Events and Did Not Meet the Criteria of a Serious Adverse Event
1.5
SECONDARY
Proportion of Rituximab Infusions in Which a Reaction to the Infusion Was Reported
0.11

Summary

Hemophilia A is a serious blood clotting disorder caused by a lack of factor VIII, a specialized protein needed for normal blood clotting to occur. Individuals with this disease may experience spontaneous bleeding, pain and swelling in their joints due to excess bleeding, and bruising. A common treatment for severe hemophilia A is to intravenously replace the deficient blood clotting factor; however, some individuals may develop antibodies to this replacement factor. This study will evaluate the effectiveness of rituximab at reducing the antibodies that develop in response to the replacement factor in individuals with severe hemophilia A.

Eligibility Criteria

Inclusion Criteria

  • Severe congenital hemophilia A
  • Documented historical inhibitor titer to factor VIII of at least 5 BU/mL
  • Inhibitor level greater than or equal to 5 BU/mL 5 to 14 days after initial factor VIII exposure during screening

Exclusion Criteria

  • Known hypersensitivities or allergies to murine and/or humanized antibodies
  • Currently participating in investigational hemophilia studies
  • HIV infected
  • Any immunodeficiency disorder
  • Liver disease and serum ALT or AST is greater than three times the upper limit of normal, albumin is less than 2.5g/dl, and/or INR is greater than 1.7
  • Received interferon or other immunomodulatory drugs, such as steroids or cytotoxic therapy in the 30 days prior to study entry
  • History of cardiac arrhythmias, any active febrile illness, kidney insufficiency, or pulmonary infiltrates
  • Has previously received rituximab treatment
  • Currently undergoing immune tolerance therapy
  • Evidence of Hepatitis B (HBV) infection, defined as one of the following:
  • HBsAg positive
  • HBsAg negative, HBsAb negative, HBcAb positive, and HBV DNA positive
  • Participants with a high responding inhibitor (at least 5 BU/mL) first detected fewer than 12 months prior to study entry, unless the participant has failed immune tolerance therapy, defined as one of the following:
  • Failure to fulfill the criteria for full or partial success within 33 months, as defined by a factor VIII recovery greater than or equal to 66% of expected and half-life greater than or equal to 6 hours measured after a 72-hour treatment-free washout period
  • Failure to achieve greater than 20% reduction in inhibitor titer during each interim non-overlapping 6-month period of ITT in the absence of documented infection, with 9 months as the minimum treatment period and 33 months as the maximum possible duration of unsuccessful ITT
  • Withdrawal from ITT for any other reason
  • Routinely receive factor VIII concentrate for the treatment of both major and minor bleeding events
  • Has received factor VIII concentrate in the 7 days prior to study entry
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00331006). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search