Velvet Therapeutics

Velvet Therapeutics

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Private Company

Total funding raised: $10M

Overview

Velvet Therapeutics is pioneering a next-generation in vivo CAR therapy platform designed to overcome key limitations of current ex vivo CAR-T approaches. Its technology utilizes a polyasparagine nanoparticle and minicircle DNA polyplex to deliver CAR genes directly into immune cells within the body, offering a redosable, non-integrating, and potentially off-the-shelf solution. The platform exhibits lymphatic tropism to avoid the hepatic sink and is initially targeting solid tumors, with its first proprietary solid tumor CAR data presented in 2025. As a private, pre-clinical stage company, Velvet aims to simplify and broaden the application of CAR therapies across immune cell types.

OncologySolid Tumors

Technology Platform

Non-viral, in vivo delivery platform using polyasparagine amino acid nanoparticles and minicircle DNA polyplexes. Engineered for lymphatic tropism to avoid hepatic clearance, enabling redosable, non-integrating reprogramming of multiple immune cell types with CAR constructs.

Funding History

1
Total raised:$10M
Seed$10M

Opportunities

The platform targets the vast, underserved solid tumor market and could democratize CAR therapy by creating a simpler, potentially redosable, and off-the-shelf alternative to complex ex vivo manufacturing.
Success would position the company as a leader in the next wave of in vivo cell therapies.

Risk Factors

The core technology is high-risk and unproven, facing significant challenges in achieving efficient in vivo delivery, durable expression, and acceptable safety.
Intense competition from other biotechs developing non-viral and in vivo approaches, coupled with the capital-intensive nature of drug development, presents substantial execution and financial risk.

Competitive Landscape

Velvet operates in a highly competitive space with numerous companies pursuing next-generation CAR therapies. Key competitors include those developing non-viral delivery methods (e.g., transposon systems, mRNA/LNP) and other in vivo CAR approaches. Large pharma and established cell therapy companies also represent significant competitive threats through internal pipelines and acquisitions.