The Diverse Biotech, asset pipeline is not a “single-drug” or “single-disease” strategy. We leverage our proprietary, patented IP repository, which contains thousands of novel, lead molecules across a wide range of drug classes. We have thousands of novel molecules.
Our short-term goal is to enhance the value of our entire IP pipeline by advancing downstream proof-of-concept studies. Each molecule proven to demonstrate increased effectiveness, and every molecule successfully licensed out, further elevates the overall value of our portfolio.
We anticipate filing an IND for our lead molecule, DBT-30180, as a first-line therapy for glioblastoma by the end of Q2 2023. FDA acceptance of this filing will significantly increase the company’s valuation and unlock numerous new licensing opportunities.
Our innovative approach redefines drug development. By starting with parent drugs that are already well-understood and FDA-approved, we reduce downstream development risk while achieving a high level of effectiveness. We combine these parent drugs with specific cannabinoids at a molecular level, creating novel molecules that outperform traditional therapies. Our new molecules demonstrate superior properties—improved efficacy, delivery, and safety—compared to the parent drug, the cannabinoid, or any conventional combination therapy using the two separately.