• June 3-6, 2024
  • San Diego Convention Center, California

Sessions

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ImmunoForge Co., Ltd.

Monday, June 03, 2024
CP
Orphan and Rare Disease
ImmunoForge is a clinical-stage, VC-backed company specializing in novel drug development based on ELP platform technology, powered by world-class expertise and focusing initially on muscular dystrophies such as Polymyositis (PM), Dermatomyositis (DM), Duchenne muscular dystrophy (DMD), Inclusion Body Myositis (IBM) and Senile Sarcopenia. ImmunoForge has an ongoing Phase 2 clinical study for its lead drug candidate PF1801 (froniglutide) for treatment of DM/PM in Korea, and has received orphan drug designation from US FDA for use of PF1801 for treatment of PM, DM and DMD. ImmunoForge is further exploiting its ELP platform technology to enable weekly injection of peptide-based drugs for DMD cardiomyopathy, achondroplasia and short bowel syndrome, and is looking for co-development or licensing partners to bring its drug candidates to market. ImmunoForge is also developing KF1601, an NCE for treatment of drug-resistant CML, including the most common resistant mutant form, BCR-ABLT315I.
ImmunoForge Co., Ltd.
Company Website: http://www.immunoforge.com
Lead Product in Development: Froniglutide
Number Of Unlicensed Products (For Which You Are Seeking Partners): Five

Company HQ City

Seoul

Company HQ State

Not applicable

Company HQ Country

Korea, Republic of

CEO/Top Company Official

Kiho Chang & Sung-Min Ahn

Development Phase of Primary Product

Phase II
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