Efficacy and safety study of a monoclonal antibody to replace steroids for treatment of patients with Granulomatosis with Polyangiitis (GPA) and Microscopic Polyangiitis (MPA) diseases.
- Conditions
- Active Granulomatosis with Polyangiitis (Wegener’s) (GPA) and Microscopic Polyangiitis (MPA)MedDRA version: 21.1Level: PTClassification code 10063344Term: Microscopic polyangiitisSystem Organ Class: 10047065 - Vascular disordersMedDRA version: 21.1Level: PTClassification code 10072579Term: Granulomatosis with polyangiitisSystem Organ Class: 10047065 - Vascular disordersTherapeutic area: Diseases [C] - Immune System Diseases [C20]
- Registration Number
- EUCTR2018-000768-27-CZ
- Lead Sponsor
- InflaRx GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 55
1. Male or female, = 18 years of age.
2. Written informed consent obtained from subject.
3. Diagnosis of GPA or MPA according to the definitions of the Chapel Hill Consensus Conference (CHCC).
4.History of positive antigen-specific ANCA testing since the time of diagnosis or at screening, or documented evidence of either anti-proteinase 3 (anti-PR3) or anti-myeloperoxidase (anti-MPO) (for newly diagnosed subjects a recent positive antigen-specific ANCA testing is mandatory for inclusion)
5. Have = 1 major” item, or = 3 other items, or = 2 renal items on the Birmingham Vasculitis Activity Score Version 3 (BVASv3).
6. Newly diagnosed or relapsed GPA or MPA that requires treatment with CYC or RTX plus GCs.
7. Estimated glomerular filtration rate (eGFR) = 20 mL/min/1.73 m².
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 50
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 5
Subjects who fulfil any of the following criteria at screening are not
eligible to participate in the study:
1.Any other multi-system autoimmune disease as listed in Appendix
18.4.
2.Require mechanical ventilation because of alveolar hemorrhage at
screening.
3.Known hypersensitivity to any investigational medicinal product (IMP)
(i.e. GC, IFX-1) and/or any excipients.
4.Subject with rare hereditary problems of galactose intolerance, total
lactase deficiency or glucose-galactose malabsorption.
5.Have required management of infections, as follows:
a.Chronic infection requiring anti-infective therapy (such as latent
tuberculosis, pneumocystis, aspergillosis, cytomegalovirus, herpes
simplex virus, herpes zoster and atypical mycobacteria) within 3 months
before screening.
b.Use of intravenous antibacterials, antivirals, anti-fungals, or anti
parasitic agents within 30 days of screening.
6.Current and/or history (within the previous 5 years) of drug and/or
alcohol abuse and/or dependence.
7.Evidence of Hep B, C and/ or HIV infection. Only subjects with
documented negative historical results (within 4 weeks before
screening) for Hep B, C Virus and HIV or a negative test by Screening
can be included into the study.
8.Any of the following abnormal laboratory findings at screening:
a.White blood cells < 3,500/mm3
b.Platelet count < 100,000/mm3
c.Transaminase values (AST and/or ALT) = 2.5 times the upper limit of
normal range (ULN)
d.Total bilirubin = 1.5 times ULN
e.Alkaline Phosphatase (ALP) > 3 times ULN
9.Current or history of malignancy, lymphoproliferative, or
myeloproliferative disorder except squamous cell or basal cell
carcinomas of the skin and cervical carcinoma in situ with curative
surgical treatment.
10.Received CYC or RTX within 12 weeks before screening or within 12
weeks before CYC or RTX is started for remission induction within 2
weeks before screening.; If subject is on AZA, MMF or MPS or MTX, these
drugs must be discontinued prior to receiving the first dose of CYC or
RTX.
11.Received > 3 g cumulative intravenous GCs within 4 weeks before
screening (RTX intravenous GC premedication is separate and does not
count to the 3 g).
12.a.Received an oral daily dose of a GC of > 10 mg prednisoneequivalent
for more than 6 weeks continuously prior to screening.
b.Received an oral daily dose of a GC of > 80 mg prednisone equivalent
within 2 weeks before screening.
13.Received a CD20 inhibitor, anti-tumor necrosis factor treatment,
abatacept, alemtuzumab, any other experimental or biological therapy,
intravenous immunoglobulin or plasma exchange, antithymocyte
globulin, or required renal dialysis within 12 weeks before screening.
14.Received a live vaccination within 4 weeks before screening or
planned between screening and Week 2774.
15.Either active or latent tuberculosis treatment is ongoing.
16.Pregnant or lactating.
17.Clinically significant abnormal electrocardiogram (ECG) during
screening.
18.Female subjects of childbearing potential unwilling or unable to use a
highly effective method of contraception (pearl index < 1) during
treatment and for at least 3 months after last administration of IFX-
1/Placebo-IFX-1 (or up to 12 months, the timeframes for Standard of
Care agents have to be considered as described in the respective
Prescribing Information/SPCstimeframes). Contraception methods
regarded as highly effective methods and the duration of contraception
are further
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: The primary objective is to evaluate the efficacy of IFX-1 treatment as a replacement for glucocorticoids [GC] therapy in subjects with GPA and MPA.;Secondary Objective: •To assess safety and tolerability of IFX-1<br>•To compare GC-induced toxicity of standard-dose GC and reduced dose GC with IFX-1 treatment<br>•To generate data for PK and PD modelling of IFX-1 treatment.<br><br>;Primary end point(s): The primary efficacy endpoint is the proportion of subjects achieving<br>clinical response defined as reduction in BVASv3 = 50% at Week 16<br>compared to Baseline (= screening assessment) and no worsening in<br>any body system. Subjects who receive rescue therapy until Week 16<br>will be considered as not having achieved clinical response.;Timepoint(s) of evaluation of this end point: Week 16
- Secondary Outcome Measures
Name Time Method Secondary end point(s): 1.Proportion of subjects with clinical response, defined as reduction in<br>BVASv3 = 50% and no worsening in any body system at each<br>measurement time point except Week 16. Subjects who receive rescue<br>therapy will be considered as not having achieved clinical response at<br>each time point later than the first administration of rescue therapy<br>2.Proportion of subjects with a clinical remission defined as having a<br>BVASv3 = 0 at Week 16<br>3.Change from baseline (=screening assessment) in BVASv3 total score<br>at Week 16<br>4.Absolute values and absolute and relative change from Day 1 in the<br>VDI at Week 16<br>5.Absolute values and absolute and relative change from Day 1 in the<br>PGA at Week 16<br>6.Absolute values and absolute and relative change from Day 1 in eGFR<br>in mL/min/1.73 m² at Week 16.;Timepoint(s) of evaluation of this end point: 1. At weeks 0 (Day 1), 1, 2, 4, 8, 12, 20, 24<br>2. Week 16<br>3. 4. and 5. From Day 1 to week 16