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RenovoRx

RenovoRx offers a targeted chemotherapy delivery platform for solid tumor cancers using its Trans-Arterial Micro-Perfusion (TAMP™) technology and FDA-cleared RenovoCath® device. The approach delivers drugs directly near the tumor site to reduce systemic exposure compared to IV chemotherapy. The company is evaluating the platform in a Phase III trial for locally advanced pancreatic cancer.

Traction –/10
Mountain View, California, United States · HQ
313K+ followers
  • Medical Devices
  • Healthcare Technology
  • Hardware
Updated 3 days ago

Funding

Raised to date

$33.2MRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.

across 4 rounds

ACRI+1

$10M · Undisclosed

Announced Mar 2026 · from article date

Disclosed cumulative: $33.2M

4/4

Founders

2 founders

Sharon Vosmek

Investor

San Francisco, United States

Since Nov 2013 · 13 yrs

Astia CEO

Ramtin Agah

Founder

RenovoRx • Founder

Product

Problem

Standard systemic chemotherapy for solid tumor cancers often results in significant toxicities and may be limited in efficacy due to poor tumor vascularization. This approach circulates therapeutic agents throughout the body, potentially leading to off-target effects and reduced drug concentration at the tumor site.

Solution

RenovoRx utilizes its proprietary Trans-Arterial Micro-Perfusion (TAMP™) therapy platform to deliver oncology agents directly to tumor sites via the peripheral vascular system. The TAMP platform, enabled by the FDA-cleared RenovoCath® device, creates a localized perfusion zone to bathe the tumor with therapeutic agents. This targeted approach aims to enhance drug efficacy by increasing concentration at the tumor while potentially minimizing systemic toxicities compared to intravenous administration. The company is currently evaluating this platform in a Phase III clinical trial for locally advanced pancreatic cancer and has begun commercial clinical use of RenovoCath® in sarcoma patients.

Target Audience

Primary users are oncologists, interventional radiologists, and clinical researchers focused on solid tumor treatments, particularly those treating pancreatic cancer. The platform is also offered at treatment centers such as Winship for locally advanced pancreatic cancer patients.

Features

  • Proprietary Trans-Arterial Micro-Perfusion (TAMP™) therapy platform for localized drug delivery
  • FDA-cleared RenovoCath® device with a dual-balloon design for temporary vessel occlusion and controlled perfusion
  • Enables targeted delivery of therapeutic agents across the arterial wall near the tumor site
  • Designed to potentially minimize systemic toxicities associated with intravenous chemotherapy
  • Currently being evaluated in a Phase III clinical trial (TIGeR-PaC) for locally advanced pancreatic cancer, with full enrollment achieved
  • Holds a portfolio of 19 issued patents and 12 pending patents related to its drug delivery technology
  • Orphan Drug Designation for its intra-arterial gemcitabine (IAG) product candidate for pancreatic and bile duct cancers
This profile is AI-generated and may contain inaccuracies.