Efficacy and Safety Study of SCT800 for On-demand Treatment With in Patients With Hemophilia A

Phase 3

• Conditions: Hemophilia A

• Registration Number: NCT02921945
• Lead Sponsor: Sinocelltech Ltd.

Brief Summary

In this trial safety and efficacy of SCT800 (B-domain deleted recombinant factor VIII) is being evaluated in 50 subjects, 12 to 65 years of age, with moderate to severe Hemophilia A. These subjects will receive open label treatment with SCT800 for approximately 6 months for on-demand treatment.

Detailed Description

Not available

Study Timeline

• Status Verified: 2016-09
• Study First Submitted: 2016-09-28
• Study First Submitted QC: 2016-09-29
• Last Update Submitted: 2016-09-29
• Study Start: 2016-10
• Study First Posted: 2016-10-03
• Last Update Posted: 2016-10-03
• Primary Completion: 2017-12
• Study Completion: 2018-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• 12 to 65 years old;
• The activity of the coagulation factor VIII (FVIII:C) ≤5%, and was previously treated with FVIII concentrate(s) for a minimum of 50 exposure days (EDs) prior to study entry
• Bleeding state need to be treated with FVIII;
• Negative assays for FVIII inhibitors (<0.6 BU/mL);
• The platelet count is normal；
• Normal prothrombin time or INR ≤1.5；
• Given informed consent

Exclusion Criteria

• Hypersensitivity to recombinant coagulation factor VIII concentrate or any of the excipients ;allergic to heterologous proteins (e.g. murine, bovine or hamster origin);
• Family history or history of FVIII inhibitors (≥0.6 Bethesda Units [BU] mL-1);
• Received an infusion of any FVIII for on-demand therapy or prophylaxis within 4 days prior to study entry (including rFVIII, plasma-derived factor VIII [pdFVIII], cryoprecipitate and whole blood);
• Significant hepatic or renal impairment (ALT and AST ≥2×ULN; BUN and Cr≥2×ULN);
• HIV seropositive;
• Abnormal hemostasis from causes other than hemophilia A；
• Patients with severe heart disease, including myocardial infarction, heart failure (III or higher level);
• Patients who received any anticoagulant or antiplatelet therapy within one week (including NSAIDs) or need to receive an anticoagulant or antiplatelet therapy during the period of clinical trials;
• Alcoholism, drug abuse, mental disorders and mental retardation;
• Elective surgery planned during the process of study;
• Patients who previously participated in the other clinical trials prior to study entry;
• The patient or parent/legal guardian is unable or unwilling to sign an informed consent form or to comply with the requirements of clinical protocol;
• Other conditions confirmed by the researchers, resulting in that patients are unable to benefit from clinical observation;

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Incremental Recovery (K-value)	1hour after the end of the infusion	One-stage aPTT Assay

Secondary Outcome Measures

Name	Time	Method
Haemostatic effect of SCT800 evaluated according to a predefined four grade scale: excellent, good, moderate, or no response	Up to 6 months
The incidence rate of FVIII inhibitors (≥0.6 BU)	Up to 6 months
The number of infusions of SCT800 required per bleeding episode	Up to 6 months
Actual consumption of SCT800 (IU/Kg/bleed)	Up to 6 months
AEs related to SCT800 during the clinical study	Up to 6 months

Trial Locations

Locations (1)

Xiangya Hospital of Centre-South University; 🇨🇳 Changsha, Hunan, China