Study of TAK-672 in Participants With Acquired Hemophilia A

JRCT ID: jRCT2051200066

Registered date:20/10/2020

Basic Information

• Recruitment status: Complete
• Health condition(s) or Problem(s) studied: Acquired Hemophilia A
• Date of first enrollment: 09/11/2021
• Target sample size: 5
• Study type: Interventional
• Intervention(s): TAK-672 will be administered at an initial dose of 200 U/kg with intravenous infusion at a rate of 1-2 mL/min. Subsequent doses will be determined based on the post-infusion FVIII:C achieved after the most recent dose given, the target FVIII:C, and porcine FVIII(pFVIII) inhibitor titer (when available)

Outcome(s)

Primary Outcome

1.Percentage of Severe Bleeding Episodes with Demonstrated Response to TAK-672 Therapy at 24 Hours after the Initiation of Treatment
Time Frame: 24 hours after the initiation of treatment
Percentage of severe bleeding episodes with demonstrated response to TAK-672 therapy at 24 hours after the initiation of treatment will be assessed by using a well-defined 4-point ordinal scale - A 'positive response' is defined as 'effective' (bleeding stopped with clinical control and FVIII:C levels of 50% or higher ) or 'partially effective' (bleeding reduced with clinical stabilization and FVIII:C levels of 20% or higher) control of bleeding, as determined by the investigator using a 4-point rating scale (effective - partially effective - poorly effective - not effective). 'Poorly effective' is defined as 'bleeding slightly reduced or unchanged and FVIII:C levels of less than 50%'. 'Not effective' is defined as 'bleeding worsening and FVIII:C levels of less than 50%'.

Secondary Outcome

1.The Overall Percentage of Severe Bleeding Episodes Successfully Controlled with TAK-672 Therapy, as Assessed by the Investigator
Time Frame: Up to 1 year (90 days after final treatment dosing)
Treatment success is defined as control of qualifying bleeding episode at the time of final treatment dosing. A severe bleeding episode is considered 'successfully controlled' if the investigator has checked 'completed TAK-672 therapy as treatment success' on the electronic case report form (eCRF).

2.The Percentage of Bleeding Episodes Responsive to TAK-672 Therapy at Designated Assessment Time Points after the Initiation of Therapy, as Assessed by the Investigator
Timeframe; Up to 1 year (90 days after final treatment dosing)
A 'positive response' is defined as 'effective' (bleeding stopped with clinical control and FVIII:C levels of 50% or higher ) or 'partially effective' (bleeding reduced with clinical stabilization and FVIII:C levels of 20% or higher) control of bleeding, as determined by the investigator using a 4-point rating scale (effective - partially effective - poorly effective - not effective). 'Poorly effective' is defined as 'bleeding slightly reduced or unchanged and FVIII:C levels of less than 50%'. 'Not effective' is defined as 'bleeding worsening and FVIII:C levels of less than 50%'.

3.Frequency of Infusions of TAK-672 Required to Successfully Control Qualifying Bleeding Episodes
Time Frame: Time of successful control of qualifying bleeding episode (varied from participant to participant)
'Frequency of infusions' will be calculated as the 'average number of infusions per day'. 'Qualifying bleeding episode' is defined as the 'initial, severe bleeding episode'

4.Total Dose of Infusions of TAK-672 Required to Successfully Control Qualifying Bleeding Episodes.
Time Frame: Time of successful control of qualifying bleeding episode (varied from participant to participant)
'Qualifying bleeding episode' is defined as the 'initial, severe bleeding episode'.

5.Total Number of Infusions of TAK-672 Required to Successfully Control Qualifying Bleeding Episodes.
Time Frame: Time of successful control of qualifying bleeding episode (varied from participant to participant)
'Qualifying bleeding episode' is defined as the 'initial, severe bleeding episode'. A severe bleeding episode is considered 'successfully controlled' if the investigator had checked 'completed TAK-672 therapy as treatment success' on the eCRF.

6.Correlation between Response to TAK-672 Therapy at Specified Time Points and Eventual Control of Severe Bleeding Episode
Timeframe; Up to 1 year (90 days after final treatment dosing)

7.Correlation among the Pre-infusion Anti-TAK-672 Antibody Titers and the Eventual Control of the Bleeding Episode
Timeframe; Up to 1 year (90 days after final treatment dosing)

8.Correlation among the Total Dose of TAK-672 and the Eventual Control of the Bleeding Episode.
Timeframe; Up to 1 year (90 days after final treatment dosing)

9.Correlation among the Response at 24 Hours and the Eventual Control of the Bleeding Episode
Timeframe; Up to 1 year (90 days after final treatment dosing)

10.Anti-hFVIII Inhibitor Level
Timeframe: Up to 1 year (90 days after final treatment dosing)

11.Anti-pFVIII Inhibitor Level
Timeframe: Up to 1 year (90 days after final treatment dosing)

12.Terminal Half-life (t1/2) for TAK-672
Timeframe: Pre-dose and at multiple time points (up to 24 hours) post-dose

13.Clearance (CL) for TAK-672
Timeframe: Pre-dose and at multiple time points (up to 24 hours) post-dose

14.Volume of Distribution (Vd) for TAK-672
Timeframe: Pre-dose and at multiple time points (up to 24 hours) post-dose

15.Area Under the Concentration-Time Curve (AUC) for TAK-672
Timeframe: Pre-dose and at multiple time points (up to 24 hours) post-dose

16.Maximum Drug Concentration (Cmax) per Dose (Cmax/Dose) for TAK-672
Timeframe: Pre-dose and at multiple time points (up to 24 hours) post-dose

17.Duration Period from Initial Dose of TAK-672 until Completion of Hemostasis Control
Timeframe: Time of completion of hemostasis control (varied from participant to participant)

18.Total Dose from Initial Dose of TAK-672 until Completion of Hemostasis Control
Timeframe: Time of completion of hemostasis control (varied from participant to participant)

19.Number of new qualified severe bleeding episodes
Timeframe; Up to 1 year (90 days after final treatment dosing)

Key inclusion & exclusion criteria

• Age minimum: >= 18age old
• Age maximum: Not applicable
• Gender: Both

Include criteria

1. Male or female Japanese participants of >=18 years of age.
2. Participants who (or their legally authorized representatives) have provided his/her written informed consent form prior to any study-related procedures and study product administration.
3. Participants with a diagnosis of AHA based on clinical evaluation and supportive local laboratory testing as shown below:
- Presentation with spontaneous bleeding without anatomical cause and without prior known bleeding disorder.
- Prolonged activated partial thromboplastin time (aPTT) without explanation.
- Abnormal aPTT cross mixing test consistent with FVIII inhibitors
- Confirmation of a low factor VIII activity ( FVIII:C).
- Positive FVIII inhibitor (>=0.6 BU) as measured either in the local or central laboratory
4. Participants with a severe bleeding episode which the investigator finds necessary to treat and whose severe bleeding episode meets at least 1 of the following criteria:
- Bleeds that pose a threat to a vital organ that could threaten life (e.g. intracranial bleed, or any site that could obstruct the airway).
- Bleeds that pose a threat to a vital organ where life is not threatened but the organ function could be impaired (e.g., intraspinal bleed threatening the spinal cord and/or nerve conduction; a continual bleed into the kidney or bladder that could result in an obstructive uropathy, testicular bleed, bleed in and around the eye).
- Bleeds requiring a blood transfusion to maintain the Hgb level at above-life or organ threatening levels (e.g. post-surgical, gastro-intestinal, retro-peritoneal, and thigh bleeds).
- Intramuscular bleeds where muscle viability and/or neurovascular integrity is significantly compromised or at risk of being compromised.
- Intra-articular bleeds impacting a major joint associated with severe pain, swelling and severe loss of joint mobility (reduced >70%) or where a bleed could result in joint destruction (e.g. in and around the femoral head).
5. Participants who are taking anti-thrombotics, (including anti-platelet agents and anticoagulants)with confirmatory laboratory testing documenting specific FVIII inhibitor titer and with 3 half-lives of the agent have elapsed since the last dose.
6. Participants with expected life expectancies of at least 90 daysprior to the onset of the hemorrhagic episode.
7. Participants of reproductive age who have agreed to use acceptable methods of contraception during the study and if female who have agreed to undergo pregnancy testing as part of the screening process.
8. Participant who are able to and willing and able to comply with the requirements of the protocol.

Exclude criteria

1. Participants with an established reason for bleeding that is not correctable even with hemostatic therapy.
2. Participants presenting a bleeding episode that is assessed likely to resolve on its own, even if left untreated.
3. Participants with a known major sensitivity (anaphylactoid reactions) to therapeutic products of porcine or hamster origin; examples include therapeutics of porcine origin (e.g. previously marketed porcine FVIII, Hyate: C) and recombinant therapeutics prepared from hamster cells (e.g. Humira, Advate, and Enbrel).
4. Participants with the use of hemophilia medication prior to the administration of TAK-672 under one of the following conditions: (1) use of "recombinant activated factor VII (rFVIIa)" within 3 hours prior to TAK-672 administration (2) use of " activated prothrombin complex concentrate (aPCC)" within 6 hours prior to TAK-672 administration or (3) use of "plasma-derived FX/FVIIa complex concentrate (pd-FX/FVIIa)" within 8 hours prior to TAK-672 administration.
5. Participants with an anticipated need for treatment or device during the study that may interfere with the evaluation of the safety or efficacy of TAK-672, or whose safety or efficacy may be affected by TAK-672.
6. Participants who are currently pregnant or breastfeeding, or planning to become pregnant or father a child during the study
7. Participants who have participated in another clinical study and has been exposed to an investigational product or device within 30 days prior to the study enrollment.
8. Participants who are scheduled to participate in another non-observational (interventional) clinical study involving an investigational product or device during the course of the study.
9. Participants who are unable to or unwilling to comply with the study design, protocol requirements, and/or the follow-up procedures.
10. Participants whose majority of age are under legal protection.
11. Participants who are an immediate family member, study site employee, or are in a dependent relationship with a study site employee who is involved in the conduct of this study (e.g. spouse, parent, child, sibling) or may consent under duress.
12. Participants who are judged by the investigator as being ineligible for any other reason.

Related Information

• Primary Sponsor: Nishizawa Atsushi
• Secondary ID(s): U1111-1258-0779,NCT04580407