Company intelligence / Profile preview

MedRegen LLC

Baltimore, Maryland, United Statesmedregenco.com ↗
Ownership
Private
Development stage
Phase 2
01

Overview

MedRegen has completed a Phase I first-in-human study showing MRG-001 is safe across all dose ranges. The intermediate dose group demonstrated significant white blood cell, stem cell, and immunoregulatory cell mobilization. The FDA has approved their IND to initiate a Phase IIa dose-ranging study for ARDS (NCT06308926). They have also completed a Phase II Wound Healing Study at Northwestern University.

Therapeutic areas
GastroenterologyPulmonologyDermatologyOtherInfectious Diseases
Modalities
Small moleculesfixed-dose drug combinations
Industry
Biotech
02

Drug pipeline

3 assets

MRG-001

2

2 more assets in the full pipeline.

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03

Partnerships

Premier CDMO (unnamed)

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