INdividualized ITI Based on Fviii(ATE) Protection by VWF

Phase 4TerminatedNCT03204539

University of California, Davis1 enrolled

Overview

The primary goal of the INITIATE trial is to compare the clinical outcome of individualized lot selection to random lot selection utilizing one plasma-derived von Willebrand factor (VWF)/coagulation factor (FVIII) complex concentrate for immune tolerance induction (ITI) in subjects with congenital Hemophilia A, FVIII activity ≤2%, and a historical high-titer inhibitor \[≥5 Bethesda Unit (BU)\].

Participants will be randomized on a one-to-one basis between one of two study arms, individualized lot selection (alternative treatment arm) and random lot selection (standard treatment arm, current US clinical practice in ITI). Study sites, participants, and investigators will be blinded to the treatment status assigned. Alternative treatment arm: Half of the participants will be randomized to blinded individualized lot selection for ITI. The target initial dose of FVIII for ITI is \~200 IU/kg/day intravenously. The suggested maximum dose is 20,000 IU/day. Investigators may adjust the dose to a minimum dose of 150 units/kg if infusion volume is not feasible in patients without central venous access or in patients with von Willebrand factor levels \>250%. Splitting dose into two infusions per day must be approved by the Steering Committee, and if approved, will be considered a protocol deviation. Wilate® will be the VWF/FVIII complex concentrate (Octapharma USA, Inc., U.S. License No. 1646) prescribed for ITI. Individualized lot selection will be performed according to a modified Oxford method in a central laboratory, by testing subject's plasma against 4-6 lots of Wilate® and selecting the one with the highest residual FVIII (lowest Oxford titer) activity remaining after incubation. The same lot will be used throughout the entire ITI course for each subject. If the selected lot is depleted prior to the completion of ITI, a second individualized lot selection will be performed using the original plasma sample provided at baseline. Each Wilate® batch includes 1.6-1.8 million IU and is expected to last for about 3-57 months depending on the weight of the subject and prescribed dose. Standard treatment arm: The other half of the participants will receive random lot selection for ITI. The dose and concentrate used will be the same. Concentrate will be randomly selected from available Wilate® lots. The same lot will be used throughout the entire ITI course for each subject. If the random lot is depleted prior to the completion of ITI, a second lot will be randomly selected. In both cases the random lot will be tested against subject's plasma to measure the residual FVIII activity left after incubation but this result will not affect lot selection. The primary hypothesis is that the time to negative inhibitor (\<0.6 BU) will be shorter with individualized lot selection compared to random lot selection and that this will impact monthly break-through bleeding and reduce costs.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Hemophilia A With Inhibitor Hemophilia A

Interventions

WilateDRUG

Wilate® is a high-purity (i.e. 100 IU FVIII/mg total protein) pdVWF/FVIII complex concentrate.Wilate® possesses all the important features asked for in ITI, namely high purity, a very high pathogen safety profile, and an excellent protection of its FVIII by VWF - all achieved through unique, novel, and innovative techniques.

Eligibility

Sex: MALE

Medical Language ↔ Plain English

Inclusion Criteria: 1. Diagnosis of congenital Hemophilia A and baseline FVIII ≤2%. 2. Weight ≥ 5 kg 3. History of FVIII inhibitor titer ≥5 BU 4. Current FVIII inhibitor titer ≥5 BU or ≥0.6 BU and failed ITI defined by FVIII recovery \<66% normal and half-life \<6 hours 5. Adequate venous access for daily concentrate infusions 6. For participants \<18 years, a parent or guardian willing and able to provide informed consent with verbal or written assent from the child if require by the local institution. For participants ≥18 years, a willingness and ability to provide informed consent from the subject. 7. Ability to comply with study related treatments, evaluations, and follow-up. Exclusion Criteria: 1. Acquired hemophilia 2. Congenital or acquired bleeding disorder in addition to Hemophilia A 3. ITI factor replacement regimen within the past one month unless there is clear evidence of ITI failure with no reduction in inhibitor titer over the past two months 4. HIV positive with viral load ≥200 particles/μL or ≥400,000 copies/mL 5. Rituximab within the past 3 months 6. IVIG within the past 1 month 7. Treatment with other immunosuppressive drugs within the past 1 month (excluding intermittent steroid use for asthma) 8. Concomitant experimental treatment 9. History of hypersensitivity to plasma-derived VWF- or FVIII-containing concentrates 10. Elective surgery planned in the next 6 months (excluding vascular access procedure) 11. Any condition or chronic illness, which in the opinion of the investigator makes participation ill-advised 12. Inability or unwillingness to complete required screening, follow-up, and exit studies

Locations (3)

University of California, Davis

Sacramento, California, United States

Rady Children's Hospital San Diego

San Diego, California, United States

Tulane University

New Orleans, Louisiana, United States

Outcomes

Primary Outcomes

Time to Negative Inhibitor

This endpoint was chosen because a shorter time to negative inhibitor should decrease monthly break-through bleeding frequency in the early phase of ITI

Time frame: completion of immune tolerance induction, up to 18 months

Secondary Outcomes

Time to Achieve Partial and Complete Success

Secondary endpoints include time to achieve partial and complete success as defined according to the following criteria: * Inhibitor titer \<0.6 BU. * Incremental in vivo FVIII recovery in the normal range \[≥66% of normal (1.5% per IU/kg), equal to 0.99%per IU/kg\] with samples taken prior to and 15 or 30 minutes after concentrate treatment. The recovery assessment should be done without any wash-out period. * Half-life of FVIII \>6 hours. The half-life assessment should be done in a non-bleeding status without any wash-out period. Complete Success (CS) of ITI: All three criteria above met. Partial Success (PS) of ITI: The first two of the three criteria above met. Partial Response (PR) of ITI: One of the three criteria above met. Partial Failure (PF) of ITI: Inhibitor still present, but titer is decreased to \<5 BU in contrast to ≥5 BU before start. Complete Failure (CF) of ITI: None of the above mentioned criteria met, and the inhibitor titer is still ≥5 BU.

Time frame: completion of immune tolerance induction, up to 18 months

Absence of Relapse, up to 12 Months After Achievement of Complete or Partial ITI Success

Time frame: one year after completion of immune tolerance induction, up to 30 months

The Number of Break-through Bleeding Events During the Course of ITI-treatment·

Time frame: completion of immune tolerance induction, up to 18 months

Cost of ITI - Including Bleeding Control Using Bypassing Agents Prior to Start and During ITI

Time frame: completion of immune tolerance induction, up to 18 months

Data from ClinicalTrials.gov

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