A Long-Term Follow-Up Study of Haemophilia B Patients Who Have Undergone Gene Therapy

Hemophilia B Clinical Trial

Official title:

An Open-Label, Multicentre, Long-Term Follow-Up Study to Investigate the Safety and Durability of Response Following Dosing of a Novel Adeno-Associated Viral Vector (FLT180a) in Patients With Haemophilia B

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03641703
• Other study ID #: FLT180a-04
• Status: Terminated
• Phase: Phase 1/Phase 2
• Start date: July 10, 2018
• Est. completion date: May 24, 2023

Study information

• Verified date: July 2023
• Source: Freeline Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Severe haemophilia B (HB) is a bleeding disorder where a protein made by the body to help make blood clot is either partly or completely missing. This protein is called a clotting factor; with severe HB, levels of clotting Factor IX (nine; FIX) are very low and affected individuals can suffer life threatening bleeding episodes. HB mainly affects boys and men (approximately one in every 30,000 males). Current treatment for HB involves intravenous infusions of FIX as regular treatment (prophylaxis) or 'on demand' treatment. On demand treatment is highly effective at stopping bleeding but cannot fully reverse long-term damage that follows after a bleed. Regular treatment can prevent bleeding; however it is invasive for patients and also expensive. This clinical study aims to investigate the long-term safety and durability of FIX activity in participants who have been dosed with a new gene therapy product (FLT180a) in earlier clinical studies. Following administration, FLT180a results in production of FIX in the participants' liver cells which is then released into the blood stream. The aim is to have the participants' own body produce levels of FIX that allow for clotting to occur as normal as would be seen in a non-HB individual. This would remove the need for prophylaxis or on demand treatment following just a single administration of FLT180a. Up to 50 participants who have already been administered with FLT180a in the EU and US will take part in this study. Participants will be followed up in this trial until they have reached 15 years after being dosed. Participants will undergo procedures including physical examinations, join assessments, blood tests and liver ultrasounds. Participants will also need to complete a diary to document occurrence of bleeding episodes and record the amount of Factor IX concentrate they receive. Patient reports outcomes including measures of Quality of Life, disability and physical activity will also be collected.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 10
• Est. completion date: May 24, 2023
• Est. primary completion date: May 24, 2023
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients who have previously received FLT180a within a clinical study.
• Able to give full informed consent and able to comply with all requirements of the study including long-term follow-up for the time frame the study requires.
• Willing to practice barrier contraception until at least three consecutive semen samples after vector administration are negative for vector sequences. Exclusion Criteria: N/A

Related Conditions & MeSH terms

• Hemophilia A
• Hemophilia B

Intervention

Biological:
• FLT180a
FLT180a is a replication-incompetent adeno-associated viral vector. The vector is composed of a DNA vector genome encapsidated in an adeno-associated virus derived protein capsid. The expression cassette contains DNA encoding Factor IX.

Locations

Country	Name	City	State
United Kingdom	The Haemophilia and Thrombosis Centre	Canterbury	Kent
United Kingdom	Royal Free London NHS Foundation Tust	London
United Kingdom	Newcastle Hemophilia Comprehensive Care Centre	Newcastle
United Kingdom	Oxford University Hospitals NHS Foundation Trust	Oxford
United Kingdom	Sheffield Teaching Hospital	Sheffield	South Yorkshire
United Kingdom	Southampton Haemophilia Comprehensive Care Centre	Southampton

Sponsors (1)

Lead Sponsor	Collaborator
Freeline Therapeutics

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary Safety Measurement	Frequency of treatment-emergent adverse events/reactions (AE/ARs) reported according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 or later (Primary Safety).	From entry to 5 years post dosing
Primary	Durability of Response	Durability of response will be estimated by the rate of decline of the FIX activity observed from study entry (Primary Endpoint)	From entry to 5 years post dosing
Secondary	Secondary Safety Measurement	Frequency of reporting of abnormal or change from baseline findings from safety assessments including laboratory assessments, vital signs, physical exam and liver ultrasound according to common terminology criteria for Adverse Events (CTCAE) version 5.0 or later.	From entry to 5 years post dosing
Secondary	FIX Activity Levels at or below 150%	Samples will be taken at each visit to measure FIX activity levels and the proportion of patients achieving FIX activity at or above 5%, 15%, 30%, 40%, 50%, 70% but no more than 150% of normal at each scheduled visit.	From entry to 5 years post dosing
Secondary	FIX Activity Levels including 150% or above	Samples will be taken at each visit to measure FIX activity levels and the proportion of patients achieving FIX activity at or above 5%, 15%, 30%, 40%, 50%, 70% and 150% of normal at each required visit.	From entry to 5 years post dosing
Secondary	FIX Activity Levels - Change from baseline	Change from baseline (prior to FLT180a dosing) in FIX activity at each scheduled visit.	From entry to 5 years post dosing
Secondary	Haemostatic Effectiveness - Bleeding Rates	Change from baseline (prior to FLT180a dosing) in annualised bleeding rate by measurement of number of breakthrough bleeding episodes.	From entry to 5 years post dosing
Secondary	Haemostatic Effectiveness - FIX Concentrate Consumption	Change from baseline (prior to FLT180a dosing) in FIX concentrate consumption by measurement of factor concentrate consumed by the patient.	From entry to 5 years post dosing
Secondary	FLT180a effectiveness related to surgical/dental procedures by assessment of consumption of exogenous clotting factors at Time of surgery, Time of drain removal (if applicable)	Consumption of exogenous clotting factors, related to an individual surgery, will be collected at the three time-points (time of surgery, time of drain removal (if applicable) and time of discharge or 6-days post surgery) for each surgery occurring from patient entry into trial until 5 years post-dosing.	From entry to 5 years post dosing
Secondary	FLT180a effectiveness related to surgical/dental procedures by assessment of measurement of absolute blood loss at Time of surgery, Time of drain removal (if applicable)	Measurement of absolute blood loss, related to an individual surgery, will be collected at the three time-points (Time of surgery, Time of drain removal (if applicable) and The earlier of discharge of 6-days post surgery) for each surgery occurring from patient entry into trial until 5 years post-dosing.	From entry to 5 years post dosing
Secondary	FLT180a effectiveness related to surgical/dental procedures by assessment of blood transfusion requirement, volume and number of transfusions at Time of surgery, Time of drain removal (if applicable)	Transfusion requirement (volume and number of transfusions), related to an individual surgery, will be collected at the three time-points (Time of surgery, Time of drain removal (if applicable) and The earlier of discharge of 6-days post surgery) for each surgery occurring from patient entry into trial until 5 years post-dosing.	From entry to 5 years post dosing
Secondary	FLT180a effectiveness related to surgical/dental procedures by assessment of efficacy of haemostasis as judged by surgeon on a 4-point scale at Time of surgery, Time of drain removal (if applicable)	Assessment of efficacy of haemostasis as judged by surgeon, related to an individual surgery, will be collected at the three time-points (Time of surgery, Time of drain removal (if applicable) and The earlier of discharge of 6-days post surgery) for each surgery occurring from patient entry into trial until 5 years post-dosing.	From entry to 5 years post dosing
Secondary	Immune response to the hFIX transgene product (i.e., development of inhibitors) will be assessed by measurement of the level of inhibitors.	Samples will be taken to capture development of inhibitors overtime.	From entry to 5 years post dosing
Secondary	Clearance of vector genomes (vgs) in plasma, urine, saliva, stool and semen.	Samples from each pool will be taken at each visit until there have been 3 consecutive samples that are negative for vgs.	From entry to complete clearance of vgs in all sample pools.