• Innovation for Regeneration

  • Innovation for Regeneration

  • Innovation for Regeneration

OVERVIEW OF COMPANY

Founded in 2017, Connext is a clinical-stage biotech company developing biological therapeutics (medicinal recombinant protein products) to improve quality of life. Based on recombinant TLR5 agonist technology, Connext is developing a therapeutic agent (first-in-class) to prevent side effects occurring during radiation and chemotherapy. Connext is also developing the world's first recombinant collagenase treatment. Connext is expanding its pipeline in the field of immuno-oncology and regenerative medicine and striving to develop and commercialize them.

HISTORY

MISSION AND VALUE

Connext is committed to improving quality of life by rapidly delivering innovative medicines and technologies to patients in the field of regenerative medicine through continual connect and innovation.

ORGANIZATION

Board of
Directors

CEO

SAB

Technology (CTO)

  • R&D
  • Process Development/scale-up
  • IP Management

Quality (CQO)

  • Method Development
  • Quality Management
  • GMP Mfg Management

Development (CDO)

  • Pre-clinical/clinical Development
  • Regulatory Affairs

Communication (CCO)

  • PR
  • Communication Channel
  • Product Marketing
  • Business Development

Operation (COO)

  • IR/Finance
  • Accounting
  • Human Resource

INVESTORS

  • KB
  • KIBO
  • LSK
  • the_wells

PIPELINE

PIPELINE
Nonclinical Phase 1 Phase 2 Phase 3
Recombinant TLR5 agonist CNT101 Acute graft-versus-host disease (aGVHD)

Acute radiation syndrome

Oral mucositis

CNT102 Cancer immunotherapy

Recombinant collagenase CNT201 Dupuytren’s contracture

Peyronie’s disease

Cellulite

CNT202 Wound debridement

MILESTONES

TLR5 agonist

Collagenase

  • 2022

  • Dupuytren’s contracture
    Phase 1/2 Pre-IND
    completed (FDA)

  • 2023

  • Acute graft-versus-host
    disease Phase 1 IND
    approved (MFDS)

  • Dupuytren’s contracture
    Phase1/2 IND
    approved (FDA)

  • 2024

  • Initiating Dupuytren’s
    contracture Phase 1/2
    clinical trials (Australia)

  • Initiating acute
    graft-versus-host
    disease clinical
    trials (MFDS)

  • 2025

  • Peyronie’s Disease
    pre-IND planned

  • Dupuytren’s
    contracture
    phase 1/2 clinical
    trials completed

BUSINESS MODEL

Promotion of commercialization through product sales rather than simple technology transfer

- Enter the market through joint development with overseas pharmaceutical companies and create technology fees and product sales.

· Establish GMP manufacturing facilities and sell drug products.
- Securing additional service and product sales based on CMC capabilities and GMP manufacturing facilities

· Service: Microbial-based recombinant protein and pDNA CDMO business
· Product: GMP grade tissue dissociation enzyme (TDzyme)

LOCATION

Head Quarter(R&D center): Suite 505, 76 Dongnae-ro, Dong-gu, Daegu, Republic of Korea
Seoul office:

Suite 1701, 322 Teheran-ro Gangnam-gu, Seoul, Republic of Korea

Bundang office:

 Suite C-03, 6th floor, Seoul National University Bundang Hospital Healthcare Innovation Park 172, Dolma-ro,
 Bundang-gu, Seongnam-si, Gyeonggi-do, Republic of KOREA

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