Development of a natural therapeutic treatment for late-stage lung cancer patients
Celtic Biotech aims to conduct Phase I Part 3 trials for CB24, a home-administered treatment for NSCLC, to secure regulatory approval and establish it as a safe, effective cancer therapy.
Projectdetails
Introduction
Celtic Biotech Ireland has developed CB24 (Crotoxin). A naturally derived receptor binding protein, delivered as monotherapy at home using infusion pumps, is hailed as a life-changing treatment for Non-Small Cell Lung Cancer (NSCLC).
Mechanism of Action
Delivered intravenously, CB24 induces predictable and consistent apoptosis (cell death) and autophagy (degradation) in human lung carcinoma cells.
Competitive Advantage
CB24 outclasses the competitive NSCLC treatment solutions (surgery, chemotherapy, and radiotherapy) through its:
- Efficacy
- Safety
- Minimal side effects
- Easy-to-use home-based treatment
- Suitability for all patients, including those at stage 3 & 4
Clinical Evidence
Celtic has already proven the efficacy of CB24 through pre-clinical and First-In-Human (FIH) clinical trials.
Project Goals
Through the proposed 24-month EIC project, the company aims to undertake Phase I Part 3 clinical trials involving 24 patients with the ultimate goal of garnering the regulatory approvals (EMA, FDA) to market the drug as a verified cancer therapeutic.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.499.999 |
Totale projectbegroting | € 3.855.337 |
Tijdlijn
Startdatum | 1-10-2023 |
Einddatum | 30-9-2025 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- CELTIC BIOTECH LTDpenvoerder
Land(en)
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