Leapfrog Bio

Leapfrog Bio

Is this your company? Claim your profile to update info and connect with investors.
Claim profile

Private Company

Total funding raised: $18M

Overview

Leapfrog Bio is a private, pre-clinical stage biotech leveraging its novel OncoSLX platform to discover and develop precision oncology therapies. The company's approach screens clinically tested drugs against a wide array of cancer driver mutations to identify potent pharmacogenetic relationships, aiming to accelerate development and reduce translational risk. Its lead program, LFB190, is a BET inhibitor targeting EP300 loss-of-function mutant cancers, with a Phase 1b/2a trial planned for 2026. A second program, LFB083, targets PIK3CA gain-of-function mutations, representing a significant unmet need in cancers like breast cancer.

Oncology

Technology Platform

OncoSLX platform: A proprietary pharmacologically-based screening platform that uses pooled CRISPR and isogenic models to test clinical-stage small molecules against cancer driver mutations, identifying pharmacogenetic relationships beyond conventional synthetic lethality.

Funding History

2
Total raised:$18M
Series A$15M
Seed$3M

Opportunities

The company addresses a large unmet need in the two-thirds of cancers driven by loss-of-function mutations, a historically 'undruggable' target class.
Its drug repurposing strategy offers a faster, de-risked development path to potentially capture significant value in niche genetic markets within major cancer indications.

Risk Factors

Key risks include the unproven clinical translation of the OncoSLX platform's predictions, competition in targeted oncology from novel drug developers, and reliance on continued venture funding as a pre-revenue, private company.
Protecting intellectual property for new methods of use is also a challenge.

Competitive Landscape

Leapfrog competes in the crowded precision oncology space but differentiates by focusing on loss-of-function mutations and drug repurposing. It faces competition from companies developing novel BET and PI3K inhibitors, as well as other platforms focused on synthetic lethality. Its success hinges on demonstrating superior efficacy in specific genetic subsets.