IP Library › Granted Patent US 12,180,274
Granted Patent B2
US 12,180,274 · App. 18/324,915 · Granted Dec 31, 2024

Treatment of pneumonia and ARDS with inhibitors of C5a and IL-6 activity

Inventors: Niels Christoph Riedemann (Jena, DE); Renfeng Guo (Ann Arbor, MI)
Assignee: InflaRx GmbH
C07K16/248A61P11/00C07K16/24C07K2317/565
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Quick Facts
Patent No.
US 12,180,274
App. No.
18/324,915
Granted
Dec 31, 2024
Kind
B2
Abstract

The present invention relates to an inhibitor of C5a activity and an inhibitor of IL-6 activity for use in the treatment of infectious pneumonia and infectious acute respiratory distress syndrome (ARDS). In further aspects administration regimes and kit of parts are referred to.

Claims (15)

1. A method of treating infectious pneumonia and/or infectious acute respiratory distress syndrome (ARDS) caused by SARS-CoV-2 infection, the method comprising:

administering to a patient in need thereof an inhibitor of C5a activity

(i) in combination with an inhibitor of IL-6 activity; and/or

(ii) wherein the patient is or has been treated with an inhibitor of IL-6 activity; and

wherein the inhibitor of C5a activity is vilobelimab and the inhibitor of IL-6 activity is tocilizumab.

2. The method of claim 1 , wherein said administering comprises a regime comprising an induction phase followed by a maintenance phase, wherein the inhibitor of C5a activity is administered in the induction phase and the maintenance phase and the inhibitor of IL-6 activity is administered:

(I) within 0-30 days prior to the induction phase,

(II) during the induction phase, and/or

(III) during the maintenance phase.

3. The method of claim 2 , wherein:

(i) the induction phase comprises or consists essentially of a period of 1 to 10 days, wherein 1-8 doses, each comprising 200-1600 mg of said inhibitor of C5a activity, are administered; and

(ii) the maintenance phase comprises or consists essentially of a period of at least 2 weeks, wherein a dose, comprising 200-1600 mg of said inhibitor of C5a activity, is administered every 1-4 weeks.

4. The method of claim 2 , wherein:

(i) 1 or 2 doses of the inhibitor of IL-6 activity is administered within 0 to 14 days prior and/or after the start of the induction phase; and/or

(ii) the inhibitor of IL-6 activity is administered at a weight dependent dose of 8 mg/kg for patients at or above 30 kg weight or 12 mg/kg for patients of less than 30 kg weight.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2023
From: RIEDEMANN, NIELS CHRISTOPH; GUO, RENFENG
To: INFLARX GMBH
Reel/Frame 064304/0509 →
Continuity (1)
Related Publication 20240391995A1 · Nov 28, 2024
Cited By (1)
US 12,697,351