Exhibitors Search

NodCure Inc.

Booth no. H50
Exhibition
|KOREA LIFE SCIENCE
Country
| Korea, South
Address
|77 Yongbong-ro, Buk-gu, Jeonnam-Gwangju, Republic of Korea
Tel
|+82-62-523-6966
E-mail
| ejsong14@nodcure.com
Exhibits
| Anti-Canine PD-L1 Antibody for Companion Animal Cancer Immunotherapy
Company Type
| Pharmaceutical / Drug Development Company , Biotech Venture / Startup

Exhibitor Information

NodCure Inc. is a biotechnology venture founded by Professor Jong-Hwan Park of the College of Veterinary Medicine at Chonnam National University.
The company develops advanced biopharmaceuticals for companion animals and microbiome-based functional ingredients.
Its lead pipeline is an anti-canine PD-L1 antibody for the treatment of canine cancer. The program is currently preparing for cell culture and process development, while clinical proof-of-concept (PoC) studies are underway to evaluate its efficacy in combination with CHOP chemotherapy. NodCure is advancing the program toward domestic regulatory approval and global licensing-out (L/O).
In addition, NodCure is expanding its business portfolio through the development of microbiome-based functional ingredients and R&D services, leveraging its proprietary microbiome research capabilities.

Exhibit Description

* Anti-Canine PD-L1 Antibody for Companion Animal Cancer Immunotherapy
1. Development of a canine-sequence IgG-based anti-PD-L1 antibody
2. Completed in vivo efficacy studies in NOG mouse models of lymphoma and osteosarcoma
3. Completion of production cell line development, RCB banking, and non-GLP toxicity study
4. Ongoing clinical efficacy evaluation in combination with the CHOP protocol

Individual Exhibit/Technology Introduction (Detailed)

  • Product Name : Anti-Canine PD-L1 Antibody for Companion Animal Cancer Immunotherapy
    * Anti-Canine PD-L1 Antibody for Companion Animal Cancer Immunotherapy 1. Development of a canine-sequence IgG-based anti-PD-L1 antibody 2. Completed in vivo efficacy studies in NOG mouse models of lymphoma and osteosarcoma 3. Completion of production cell line development, RCB banking, and non-GLP toxicity study 4. Ongoing clinical efficacy evaluation in combination with the CHOP protocol 5. Target by 2027: Establishment of cell culture and manufacturing process development, scale-up production, and completion of a GLP single-dose toxicity study
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