CSL Behring Sclero XIII

Sponsor

University College, London (Other)

Overall Status

Unknown status

CT.gov ID

NCT02551042

Collaborator

CSL Behring (Industry)

Enrollment

Location

Arms

Duration (Months)

0.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Many patients with Scleroderma (Systemic sclerosis) experience damage to blood vessels, mainly to the small arteries. A common manifestation of this is Raynaud's phenomenon (fingers or toes turning white then blue in the cold) and digital ulcers (open sores on the fingertips). The purpose of this study is to see how effective the study drug Human Factor XIII Concentrate is in treating patients who have these and other common manifestation of Scleroderma. It will be given in addition to the accepted treatments used for this disease.

Condition or Disease	Intervention/Treatment	Phase
Systemic Sclerosis	Drug: Fibrogammin®P, coagulation factor XIII concentrate (Human) Drug: 0.9% sodium chloride	Phase 2

Detailed Description

This is a phase II, double-blind, randomized, placebo-controlled study to investigate pharmacokinetics (PK), safety and efficacy of intravenous factor XIII treatment in patients with systemic sclerosis.

Scleroderma (Systemic sclerosis) is a multisystem rheumatic disease that is characterised by progressive vascular damage e.g Raynaud's phenomenon and digital ulcers and organ fibrosis e.g. skin thickening and pulmonary fibrosis.The disease is associated with significant morbidity and mortality and current therapeutic options are only partially effective, including Cyclophosphamide for skin or lung fibrosis and Bosentan which reduces but does not heal digital ulcers.

There is no cure available and there is therefore a high need for new therapeutic options.Administration of human Factor XIII (FXIII) concentrate in patients with scleroderma demonstrated promising results in the 1980s and 1990s . However these studies were not performed according to current Good Clinical Practice (GCP) guidelines and involved relatively small sample sizes.

This is a single site study, therefore all study participants will be seen at the Royal Free London National Health Service (NHS) Foundation Trust.Total study duration is 36 months and will involve 2 phases: an initial single dose, pharmacokinetic (PK) phase in 8 subjects over 6 weeks and a multiple dose, active treatment phase in 18 subjects over 24 weeks. During the treatment phase subjects will be randomized at 2:1 ratio to either FXIII or Placebo and will receive biweekly injection of either factor XIII Concentrate or placebo.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

26 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Triple (Participant, Care Provider, Investigator)

Primary Purpose:

Treatment

Official Title:

A Phase II, Double-blind, Randomized, Placebo-controlled Study to Investigate Pharmacokinetics (PK), Safety and Efficacy of Intravenous Factor XIII Treatment in Patients With Systemic Sclerosis

Study Start Date :

Sep 1, 2015

Anticipated Primary Completion Date :

Sep 1, 2016

Anticipated Study Completion Date :

Sep 1, 2018

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Active treatment arm Fibrogammin®P, coagulation factor XIII concentrate (Human) IV infusion	Drug: Fibrogammin®P, coagulation factor XIII concentrate (Human) IV infusion Other Names: Factor XIII
Placebo Comparator: Placebo arm Placebo will be 0.9 % Sodium chloride solution IV infusion	Drug: 0.9% sodium chloride IV infusion Other Names: Normal saline

Arm

Intervention/Treatment

Experimental: Active treatment arm

Fibrogammin®P, coagulation factor XIII concentrate (Human) IV infusion

Drug: Fibrogammin®P, coagulation factor XIII concentrate (Human)

IV infusion

Other Names:

Factor XIII

Placebo Comparator: Placebo arm

Placebo will be 0.9 % Sodium chloride solution IV infusion

Drug: 0.9% sodium chloride

IV infusion

Other Names:

Normal saline

Outcome Measures

Primary Outcome Measures

Primary outcome assessed by skin involvement measured with modified Rodnan skin score [24 weeks]
Primary outcome assessed by skin involvement measured with Raynaud condition score [24 weeks]

Secondary Outcome Measures

Pulmonary function measured by pulmonary function test [24 weeks]
Pulmonary function measured by pulmonary function test
Hand function measured with Cochin hand function [24 weeks]
Hand function measured with Cochin hand function
Quality of life measured with Short Form-36 (SF-36) quality of life questionnaire [24 weeks]
Quality of life measured with SF36 quality of life questionnaire
Number of new digital ulcers (DU) [24 weeks]
Prevention of new DU: Number of new DU developed during a 24-week period of treatment
Complete healing of digital ulcers (DU) [24 weeks]
Healing of DU: Complete healing of DUs present at baseline; each DU is considered as an entity
Digital ulcer pain assessment [24 weeks]
DU Pain assessment at 4, 8, 12, 16, 24 weeks of treatment: Pain will be assessed by analogue scale for pain (Visual Analogue Scale, VAS)
Digital ulcer pain assessment [24 weeks]
DU Pain assessment at 4, 8, 12, 16, 24 weeks of treatment: Pain will be assessed by Raynaud's severity (Raynaud's condition score)
Digital ulcer worsening: hospitalisation required [24 weeks]
Number of overnight hospitalisations for digital ulcers
Digital ulcer worsening: surgical intervention required [24 weeks]
Number of additional surgical treatments for digital ulcer in outpatient clinic
Digital ulcer worsening: Digital ulcer infection [24 weeks]
Number of digital ulcers with infections
Digital ulcer worsening: Gangrene [24 weeks]
Number of episodes of gangrene
Digital ulcer worsening: Amputation [24 weeks]
Number of amputations
Digital ulcer worsening: Need of local sympathectomy [24 weeks]
Number of local sympathectomies
Digital ulcer worsening: Need of toxin Botulinum A [24 weeks]
Number of treatments with Botulinum toxin A
Digital ulcer worsening: Need of oral or parenteral antibiotic [24 weeks]
Number of treatments needed with oral or parenteral antibiotic
Digital ulcer worsening: Need of intravenous (IV) Iloprost : this is considered treatment failure [24 weeks]
Number of treatments needed with intravenous (IV) Iloprost : this is considered treatment failure

Other Outcome Measures

Safety endpoints: Physical examination (including height, weight, BMI, digital ulcer characterization) [24 weeks]
Physical examination (including height, weight, BMI, digital ulcer characterization)
Safety endpoints: Adverse events [24 weeks]
Adverse events
Safety endpoints: Serious adverse events [24 weeks]
Serious adverse events
Safety endpoints: ECG [24 weeks]
ECG
Safety endpoints: Vital signs [24 weeks]
Vital signs
Safety endpoints: Clinical laboratory parameters [24 weeks]
Clinical laboratory parameters
Safety endpoints: Pregnancy [24 weeks]
Serum or urine pregnancy tests will be performed at each visit and will be reported positive or negative
Safety endpoints -Adverse events of special interest: thromboembolic events [24 weeks]
Adverse events of special interest: thromboembolic events

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male and female adults.
Subjects with a diagnosis of systemic sclerosis (scleroderma, SSc) according to the 2013 American College of Rheumatology European League Against Rheumatism (ACR EULAR) classification criteria. They will be classified according to LeRoy criteria as limited or diffuse subset.
Females of childbearing potential must be willing to use a reliable form of medically acceptable contraception and have a negative pregnancy test.
Subjects will have serological status for hepatitis A and B assessed at screening.
Patients who have given their free and informed consent. -≥ 18 years.

Exclusion Criteria:

Participants must:

Be willing to use an effective method of contraception (hormonal or barrier method of birth control; abstinence) from the time consent is signed until 6 weeks after treatment discontinuation (females of childbearing potential and males)
Have a negative pregnancy test within 7 days prior to being registered for trial treatment (females of childbearing potential). NOTE: Subjects are considered not of child bearing potential if they are surgically sterile (i.e. they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal.
Not be breastfeeding (females).

Participants must not:

Have allergies to excipients of the investigational medicinal product (IMP) and placebo
Have uncontrolled systemic hypertension as evidenced by sitting systolic blood pressure ≥ 160 mmHg or sitting diastolic blood pressure ≥ 100 mmHg.
Have portal hypertension or chronic liver disease defined as mild to severe hepatic impairment (Child-Pugh Class A-C). Subjects positive for Hepatitis C with evidence of active viral replication on sensitive polymerase chain reaction (PCR) testing are also excluded.
Have hepatic dysfunction, defined as aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) ≥ 3 times the upper limit of the normal range (× ULN) at the Screening Visit.
Have chronic renal insufficiency as defined by a serum creatinine ≥ 2.5 mg/dL (≤ 221 micromol/L) or requires dialysis.
Have a haemoglobin concentration ≤ 10 g/dL (≤ 100 g/L) at the Screening Visit.
Have a history of left-sided heart disease and/or clinically significant cardiac disease, including but not limited to any of the following: aortic or mitral valve disease (stenosis or regurgitation) defined as more than minimum aortic insufficiency and more than moderate mitral regurgitation (stenosis or regurgitation≥ grade 1); pericardial constriction; restrictive or congestive cardiomyopathy; left ventricular ejection fraction ≤ 40 % by multiple gated acquisition scan (MUGA), angiography, or echocardiography; left ventricular shortening fraction ≤ 22 % by echocardiography; or symptomatic coronary disease with demonstrable ischemia.
Have a history of malignancies within 5 years of Screening Visit with the exception of localized skin or cervical carcinomas.
Have psychiatric, addictive, or other disorder that compromises the ability to give informed consent for participating in this study. This includes subjects with a recent history of abusing alcohol or illicit drugs.
Be receiving ongoing treatment with hyperbaric oxygen
Have pulmonary artery hypertension (PAH)
Have received IV Iloprost within the last 2 months
Have been treated with sympathectomy or toxin botulinum A within the last 3 months
Have had thrombosis, stroke, pulmonary embolism or myocardial infarction in the last 6 months
Have a diagnosis of diabetes mellitus requiring dietary restriction of carbohydrate.
Be on a low sodium diet on medical advice.
Be participating in another clinical trial involving an investigational medicinal product.