MMI-0100

Overview

Treatment of idiopathic pulmonary fibrosis and other actue fibrotic indications

Moerae Matrix’s first development candidate, MMI-0100, is in preclinical development for treatment of idiopathic pulmonary fibrosis and other acute fibrotic indications. In the bleomycin mouse model, the industry standard model of pulmonary fibrosis, many agents are able to demonstrate anti-fibrotic activity when dosed prophylactically, prior to the onset of fibrosis. However, MMI-0100 has the unique ability to show a therapeutic benefit by abrogating collagen deposition when dosed after the onset of fibrosis.

MMI-0100’s anti-fibrotic activity is consistent in models of multiple fibrotic conditions including vascular intimal hyperplasia, post-surgical adhesions, and cutaneous scarring. Across model systems, MMI-0100 demonstrates excellent in vivo potency. The company has compiled a full IND-enabling data package on MMI-0100; the compound also demonstrates a favorable toxicology profile and highly scalable manufacturing process. In support of chronic administration for treatment of IPF, the company is developing a pulmonary formulation of MMI-0100 for dry powder inhalation delivery.


Status


Purdue Faculty

Dr. Alyssa Panitch formerly of Purdue, now of UC Davis


Clinical Trial Information

Phase 1 Trial - Phase 1a Study in Healthy Smokers to Investigate the Effect With MMI-0100 on Airway Inflammation in Induced Sputum After Challenge With Inhaled Lipopolysaccharide (LPS)


Development Partner

Moerae Matrix

Research Articles

Inhibition of Mitogen Activated Protein Kinase Activated Protein Kinase II with MMI-0100 reduces intimal hyperplasia ex vivo and in vivo

MMI-0100 inhibits cardiac fibrosis in myocardial infarction by direct actions on cardiomyocytes and fibroblasts via MK2 inhibition