Study of Efficacy and Safety of FRSW107 in Pediatric Patients With Severe Hemophilia A

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexMale
Age1-12
SponsorJiangsu Gensciences lnc.

About this trial

This study was divided into four stages: screening period, main trial period, extension period and follow-up period.

In the main trial, both groups received FRSW107 prophylactic therapy. The recommended initial dose of prophylactic administration was 50 IU/kg, the dose range was 25 to 50 IU/kg, and the recommended frequency of administration was once every three days (Q3D). The dose range could be adjusted according to the patient's response. The main trial period was prophylaxis up to ≥50 exposure days (EDs) and ≥6 months.

The investigator may adjust the dose according to the clinical efficacy of the subjects (the occurrence of bleeding and its clinical manifestations) and the concentration of FⅧ valley according to the following principles.

If necessary, the investigator may adjust the dosing interval according to the clinical efficacy of the subject (the occurrence of bleeding and its clinical manifestations) and the concentration of FⅧ. Investigators are advised to inform sponsors or their research partners when adjusting doses and dosing intervals during prophylaxis.

After participants completed prophylaxis until ≥50EDs and ≥6 months, participants' willingness and investigator evaluation were used to decide whether to enter the extended trial. All subjects entering the extended phase continued with the original prophylactic regimen until 100EDs was dosed.

During the main trial period and the extended preventive treatment period, if the subjects have breakthrough bleeding events requiring treatment, hemostatic treatment of breakthrough bleeding with investigational drugs can be performed. The researchers can refer to the treatment guidance for different degrees of bleeding in Table 6-1. Taking into account the subject's prophylactic dose, severity of bleeding, site and extent of bleeding, clinical status, and previous PK results (if any), the investigator determines the appropriate dose to administer (recommended dose range: 25 to 50 IU/kg) and dosing times until the investigator assessed significant control of bleeding episodes (e.g. reduction of pain and swelling) or return to pre-bleeding activity. If the bleeding episode stops, the subject will continue with the same dose and frequency of prophylactic medication as before the bleeding episode.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Children <12 years old, male;

Weight >10kg;

clinically confirmed patients with severe hemophilia A (defined as confirmation at the time of screening or previous medical records: coagulation factor VI activity <1%);

Treated patients, that is, those who had previously received EVI treatment and met the following criteria: <6 years old patients who had been treated with coagulation factor VI for >50 exposure days (EDs250), and < 26 years old patients who had been treated with coagulation factor VI for >150 exposure days(> 150);

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • FRSW107

    Drug

    experimental:Q3D.≥50EDs, Expansion phase:Q3D.100EDs

Treatment groups

76 Participants
are divided into 1 treatment group
Group A: The main test period and the extension periodExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

ABR

Number of bleeding during the treatment period/(Number of treatment days /365.25)

Time frame
1year

Secondary outcomes

1

AJBR

annual rate of spontaneous joint bleeding and annual rate of traumatic joint bleeding

Time frame
1year
2

AE/ADR

Frequency and severity of all AE/ADR and SAE/SAR

Time frame
1year
3

Incidence of positive FⅧ inhibitor

Bethesda method improved by Nijmegen was adopted. Generally, the titers of 20.6 BU/ml were positive for two tests within 1-4 weeks. In addition to the screening period, FV1 inhibitor detection results 137/137Scheme number: SS-107-11103 ConfidentialVersion number: 4.0 Version Date: 07H August 2023The titer was 20.6 BU/ml, and retesting was scheduled within 1-4 weeks. At any visit, a minimum 72-hour FV1 washout period was required before collection of inhibitor test samples.

Time frame
1year
4

Cmax

Cmax

Time frame
1year

Other outcomes

1

Functional Independence Score in Hemophilia

FISH incorporates items that are perceived as important by persons with hemophilia, is performance based, and is relatively safe to perform.The higher the rating, the better

Time frame
1 year
2

Pediatric Quality of Life Inventory

The higher the rating, the better

Time frame
1 year

Sponsors and contacts

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