METHODS AND COMPOSITIONS FOR TREATING IgG4-RELATED DISEASES
AssigneeZenas BioPharma, Inc.
InventorsAllen POMA, Shauna QUINN, Xiaodong WANG
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Abstract
The present invention provides compositions and methods of treating and improving the symptoms of IgG4-RD using an antibody or antigen-binding fragment thereof that specifically binds human CD19.
Claims25
A method of treating IgG4-related disease (IgG4-RD), comprising administering obexelimab subcutaneously to a human patient at least 18 years of age at a dose of 250 mg once a week.
The method of any one of the preceding claims, wherein the human patient has received glucocorticoid (GC) therapy.
The method of claim any one of the preceding claims, wherein obexelimab is administered for a time period sufficient to improve, stabilize or reduce one or more symptoms of IgG4-RD relative to a control.
The method of any one of the proceeding claims, wherein obexelimab is administered to the patient to improve clinical symptoms.
The method of any one of the preceding claims, wherein obexelimab is administered to the human patient during a recurrence-free period to prevent relapse.
The method of any one of the proceeding claims, wherein obexelimab is administered to the patient until the patient has active IgG4-RD disease flare that requires initiation of rescue therapy.
The method of any of the preceding claims, wherein the human patient is relapsed or refractory to a previous treatment for IgG4-RD.
The method of any of one of the preceding claims, wherein the human patient is assessed for disease activity using the IgG4-RD responder index (RI).
The method of any of one of the preceding claims, wherein the human patient achieves a ≥2 points decrease in IgG4-RD RI from day 1 of administration with obexelimab.
The method of any of one of the preceding claims, wherein the human patient has American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) classification criteria for IgG4-RD score (IgG4-RD score) ≥20 prior to administration of obexelimab.
The method of any one of the preceding claims, wherein the human patient presents with IgG4-RD manifestation selected from the group consisting of IgG4-related sialadenitis (chronic sclerosing sialadenitis, Kuttner's tumour, Mikulicz's disease), IgG4-related dacryoadenitis (Mikulicz's disease), IgG4-related ophthalmic disease (idiopathic orbital inflammatory disease, orbital pseudotumor), chronic sinusitis IgG4-related hypophysitis (IgG4-related panhypophysitis, IgG4-related adenohypophysitis, IgG4-related infundibuloneurohypophysitis, autoimmune hypophysitis), IgG4-related pachymeningitis, IgG4-related leptomeningitis (idiopathic hypertrophic pachymeningitis), IgG4-related pancreatitis (Type 1 autoimmune pancreatitis, IgG4-related AIP, lymphoplasmacytic sclerosing pancreatitis, chronic pancreatitis with diffuse irregular narrowing of the main pancreatic duct), IgG4-related lung disease (Pulmonary inflammatory pseudotumour), IgG4-related pleuritis, IgG4-related hepatopathy, IgG4-related sclerosing cholangitis, IgG4-related cholecystitis, IgG4-related aortitis (inflammatory aortic aneurysm), IgG4-related periaortitis (chronic periaortitis), IgG4-related periarteritis, IgG4-related pericarditis, IgG4-related mediastinitis (fibrosing mediastinitis), IgG4-related retroperitoneal fibrosis (retroperitoneal fibrosis, Albarran-Ormond syndrome, Ormond's disease (retroperitoneal fibrosis), perirenal fasciitis, Gerota's fasciitis/syndrome, periureteritis fibrosa, sclerosing lipogranuloma, sclerosing retroperitoneal granuloma, non-specific retroperitoneal inflammation, sclerosing retroperitonitis, retroperitoneal vasculitis with perivascular fibrosis), IgG4-related mesenteritis (subtypes are:
- mesenteric panniculitis, mesenteric lipodystrophy and retractile mesenteritis) (sclerosing mesenteritis, systemic nodular panniculitis, liposclerosis mesenteritis, mesenteric Weber-Christian disease, mesenteric lipogranuloma, xanthogranulomatous mesenteritis), IgG4-related mastitis (sclerosing mastitis), IgG4-related kidney disease (IgG4-RKD), IgG4-related tubulointerstitial nephritis (IgG4-TIN), IgG4-related membranous glomerulonephritis (idiopathic tubulointerstitial nephritis), IgG4-related prostatitis, IgG4-related perivasal fibrosis (chronic orchialgia), IgG4-related paratesticular pseudotumor, IgG4-related epididymo-orchitis (paratesticular fibrous pseudotumor, inflammatory pseudotumor of the spermatic cord, pseudosarcomatous myofibroblastic proliferations of the spermatic cord, proliferative funiculitis, chronic proliferative periorchitis, fibromatous periorchitis, nodular periorchitis, reactive periorchitis, fibrous mesothelioma), IgG4-related lymphadenopathy, IgG4-related skin disease (angiolymphoid hyperplasia with eosinophilia, cutaneous pseudolymphoma), IgG4-related perineural disease, and IgG4-related thyroid disease (Reidel's thyroiditis), inflammatory pseudotumour, and multifocal fibrosclerosis.
The method of anyone of the preceding claims, wherein the human patient presents an IgG4-RD manifestation selected from the group consisting of autoimmune pancreatitis (lymphoplasmacytic scleorising pancreatitis), eosinophilic angiocentric fibrosis (affecting the orbits and upper respiratory tract), fibrosing mediastinitis, idiopathic hypertrophic pachymeningitis, idiopathic tubulointerstitial nephritis, inflammatory pseudotumour, Kuttner's tumour, Mikulicz's disease, fibrosclerosis, periaortitis, periarteritis, inflammatory aortic multifocal aneurysm, Ormond's disease (tetroperitoneal fibrosis), Riedel's thyroiditis, and sclerosing mesenteritis.
Dependencies are inferred from the claim text.