RenovoRx
RenovoRx develops targeted oncology therapies using its TAMP platform and FDA-cleared RenovoCath dual-balloon catheter. The company serves U.S. cancer centers treating solid tumors, with primary focus on locally advanced pancreatic cancer through device commercialization and the Phase III TIGeR-PaC trial.
- Company typePublic
- Founded2009
- HeadquartersMountain View, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What RenovoRx does
RenovoRx, Inc. is a clinical-stage biopharmaceutical company headquartered in Mountain View, California, founded in 2009 and publicly traded on Nasdaq under the ticker RNXT. The company develops targeted oncology therapies with a primary focus on locally advanced pancreatic cancer (LAPC) and other solid tumors with poor blood supply, where standard systemic intravenous chemotherapy is limited in effectiveness and accompanied by debilitating side effects. RenovoRx serves U.S. cancer centers—primarily high-volume National Cancer Institute (NCI)-designated cancer centers and academic medical centers performing interventional oncology procedures—and is expanding its commercial footprint alongside ongoing clinical development.
The company's core technology is the Trans-Arterial Micro-Perfusion (TAMP) therapy platform enabled by the patented, FDA 510(k)-cleared RenovoCath dual-balloon occlusion catheter, which received FDA clearance in 2014. The TAMP approach leverages the vasa vasorum pathway to deliver chemotherapy across the arterial wall near the tumor site, with the dual-balloon design isolating vessel sections to create localized intra-arterial pressure that drives therapeutics across the vessel wall. RenovoRx's lead investigational drug-device combination product candidate is IAG (intra-arterial gemcitabine), currently being evaluated in the Phase III TIGeR-PaC trial under FDA's 21 CFR 312 pathway. The company has secured three FDA Orphan Drug Designations—IAG for pancreatic cancer, IAG for bile duct cancer, and oxaliplatin for pancreatic cancer (granted May 2026)—each providing 7 years of market exclusivity upon NDA approval. The IP portfolio comprises 19 issued patents across multiple countries, including 9 U.S. patents and 7 pending, with the first Japanese patent allowed in April 2026.
RenovoRx generates revenue primarily through sales of the RenovoCath device as a stand-alone Class II medical device to U.S. cancer centers on a negotiated per-procedure basis. First commercial purchase orders were received in December 2024, with FY2025 revenue reaching $1.1 million and Q1 2026 revenue of $563,000 representing 136% quarter-over-quarter and 186% year-over-year growth. The company has reiterated FY2026 revenue guidance of $3-4 million. As of May 6, 2026, RenovoRx has 16 active commercial cancer center customers (up from 5 at the start of 2025) with 32 additional centers in the pipeline, targeting 36 active centers by year-end 2026. The company pursues a direct field sales motion targeting physician-to-physician advocacy at interventional oncology programs, supplemented by investigator-initiated trials, the PanTheR post-marketing registry launched July 2025, and the potential addition of a medical device commercial partner for scaled distribution.
RenovoRx firmographics
Firmographics- Name
- RenovoRx
- Legal name
- RenovoRx, Inc.
- Website
- https://renovorx.com
- Company type
- Public
- Founded year
- 2009
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- RenovoRx develops targeted oncology therapies using its TAMP platform and FDA-cleared RenovoCath dual-balloon catheter. The company serves U.S. cancer centers treating solid tumors, with primary focus on locally advanced pancreatic cancer through device commercialization and the Phase III TIGeR-PaC trial.
- Ownership category
- akta.pro rank
RenovoRx industry classification
Industry- Product category
- Oncology Medical Devices
- NAICS
- Pharmaceutical Preparation Manufacturing (325412), In-Vitro Diagnostic Substance Manufacturing (325413)
- SIC
- Surgical & Medical Instruments & Apparatus (3841)
- akta.pro primary industry
- Gastrointestinal Oncology (HLAKAFAK)
- akta.pro secondary industries
- Nephrology & Urology Pharmaceuticals (HLAIAAAM), DTx/SaMD Deployment, Integration & Reimbursement Enablement (HLACANAO)
Keywords
Where RenovoRx is headquartered
LocationHeadquarters
- HQ city
- Mountain View
- HQ country
- United States
- HQ region
- North America
Offices2 records
Markets served
RenovoRx business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Marketing or Sales, Operations
Revenue model
- RenovoCath Device Sales: Sale of the FDA-cleared RenovoCath dual-balloon drug-delivery device as a stand-alone medical device to U.S. cancer centers. One-time hardware sales of a Class II medical device. First commercial purchase orders received December 2024. 2024 revenue: $43,000; Q4 2025 revenue: $238,000; Full year 2025 revenue: $1.1 million; Q1 2026 revenue: $563,000 (136% QoQ growth, 186% YoY growth). Reiterated full year 2026 revenue guidance of $3-4 million. Repeat-order behavior observed from existing customers. Estimated initial TAM of approximately $400 million peak annual U.S. sales opportunity for RenovoCath as a stand-alone device, with long-term several-billion-dollar potential as the platform expands into additional solid tumor indications.
- Future Drug-Device Combination Revenue (IAG): Future potential revenue stream from the investigational drug-device combination product IAG (intra-arterial gemcitabine delivered via RenovoCath) if approved following the Phase III TIGeR-PaC clinical trial. Currently under investigation and not yet approved for commercial sale. Would offer 7 years of market exclusivity upon FDA NDA approval based on three existing Orphan Drug Designations.
- Post-Marketing Registry Study Revenue Pathway: Launched in July 2025, the PanTheR post-marketing registry evaluates cancer treatment delivered by RenovoCath in solid tumors to expand safety and performance data, generating capital-efficient clinical evidence. The University of Vermont Cancer Center completed the first registry-eligible patient procedure, with additional sites including Baptist Health Miami Cancer Institute. This pathway may generate incremental revenue while expanding clinical evidence.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Other | Pay-as-you-go | Quote-based / not publicly disclosed; revenue is generated per device sold and per procedure performed at cancer centers |
Go-to-market motion3 records
Distribution channels4 records
Marketing channels8 records
RenovoRx product offering
Product offeringCore offering
RenovoRx develops and commercializes the FDA 510(k)-cleared RenovoCath dual-balloon catheter device and its proprietary Trans-Arterial Micro-Perfusion (TAMP) therapy platform for targeted intra-arterial delivery of chemotherapy to treat solid tumors. The company sells RenovoCath as a stand-alone medical device to U.S. cancer centers and is advancing the investigational drug-device combination IAG (intra-arterial gemcitabine) through the Phase III TIGeR-PaC clinical trial for locally advanced pancreatic cancer.
Product overview
RenovoRx develops a unified targeted oncology platform combining its FDA-cleared RenovoCath® dual-balloon drug-delivery device with its proprietary Trans-Arterial Micro-Perfusion (TAMP™) therapy platform. The core RenovoCath device enables localized delivery of therapeutic agents directly near tumors, while the TAMP platform powers investigational drug-device combination products such as IAG (intra-arterial gemcitabine) for treating locally advanced pancreatic cancer (LAPC).
Differentiator
Problem solved
Functional benefit
Brands
- RenovoCath: FDA-cleared dual-balloon drug-delivery device for targeted local delivery of chemotherapy
- TAMP (Trans-Arterial Micro-Perfusion)
- TIGeR-PaC
Products and services
- RenovoCath Dual-Balloon Occlusion Catheter FDA 510(k)-cleared double-balloon infusion catheter designed for isolation of blood flow and delivery of fluids, including diagnostic and therapeutic agents, to selected sites in the peripheral vascular system. Indicated for temporary vessel occlusion in arteriography, preoperative occlusion, and chemotherapeutic drug infusion in arteries 3mm and larger. Sold to U.S. cancer centers as a stand-alone medical device.
- IAG (Intra-Arterial Gemcitabine) Drug-Device Combination Investigational drug-device combination oncology product candidate utilizing RenovoCath for the intra-arterial administration of gemcitabine. Regulated under FDA's 21 CFR 312 IND pathway and under investigation in the Phase III TIGeR-PaC clinical trial for locally advanced pancreatic cancer (LAPC).
Quantifiable outcome
- 52% reduction in tumor metabolic activity at 4-month follow-up (PET-CT) in an 82-year-old LAPC patient treated via TAMP/RenovoCath (Moffitt Cancer Center case study)
- +6 more outcomes
Companies that use RenovoRx
Customer profileNamed customers17 records
Segments2 records
Ideal customer profiles2 records
RenovoRx technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Integration1 record
Feature5 records
RenovoRx partnerships and signals
Strategic signalPartnerships
15 partnerships are on record, tiered minor, flagship and core.
- Alliance Global Partners (AGP)minorHosted by Scott Henry, AGP's Managing Director and Senior Healthcare Analyst. AGP Annual Healthcare Company Showcase (May 20, 2026) featured CEO Shaun Bagai and CFO Mark Voll discussing commercial progress, RenovoCath adoption, and TIGeR-PaC trial updates.
- U.S. Interventional Radiology Experts (RenovoCath Medical Advisory Board)flagshipRenovoRx formed a six-member RenovoCath Medical Advisory Board comprising leading U.S. interventional radiology experts: Nadine Abi-Jaoudeh, MD (UC Irvine), Mustafa Al-Roubaie, MD (Moffitt Cancer Center), Khashayar Farsad, MD, PhD (Oregon Health & Science University), Ripal Gandhi, MD (Baptist Health South Florida), Paula Marie Novelli, MD (University of Pittsburgh Medical Center), and Jonathan Kessler, MD (City of Hope). The board provides strategic clinical insights, supports investigator-initiated trials in pancreatic cancer, and provides feedback to the sales and marketing team.
- AlphaNorth Capital EventminorInvestor conference held January 16-18, 2026 in Nassau, Bahamas where CEO Shaun Bagai discussed RenovoRx's progress on targeted oncology therapies and the commercialization of RenovoCath.
- iAccess AlphaminorInvestor conference partner hosting the Virtual Best Ideas Winter Investment Conference 2025 (December 9, 2025) and Summer Investment Conference 2026 (June 23-24, 2026) where CEO Shaun Bagai presented RenovoRx's clinical progress and commercial efforts.
- Canaccord Genuity MedTech, Diagnostics & Digital Health & Services ForumminorForum held November 20, 2025, where CEO Shaun Bagai discussed RenovoRx's clinical progress and market demand for the RenovoCath device.
- KCSA Strategic CommunicationscoreRenovoRx's investor relations communications partner. Provides IR outreach and contact for one-on-one investor meetings. Contact: Valter Pinto or Jack Perkins, T: 212-896-1254, [email protected]. Listed as Investor Relations Contact on multiple press releases.
- STiR CommunicationscoreRenovoRx's media relations partner. Contact: Hannah Williams, T: 803-521-1214, [email protected]. Listed as Media Contact on press releases.
- Society of Interventional Radiology (SIR)coreRenovoRx regularly presents clinical data at SIR Annual Scientific Meetings. The 2026 SIR Annual Scientific Meeting in Toronto, Canada featured a clinical data abstract from Moffitt Cancer Center experts supporting RenovoRx's TAMP therapy platform. Sponsorship and presentation at SIR is a recurring element of the company's conference marketing strategy.
- American Society of Clinical Oncology (ASCO)coreRenovoRx presents Phase III TIGeR-PaC clinical trial sub-study data at ASCO meetings. The 2026 ASCO Annual Meeting (May 29 – June 2, 2026, Chicago) published online the PK/PD sub-study abstract E16463. ASCO GI Cancers Symposium 2026 also hosted RenovoRx's TIGeR-PaC sub-study data.
- Society of Interventional Oncology (SIO)coreRenovoRx regularly presents at SIO Annual Scientific Meetings. SIO 2026 (February 4-8, 2026, Savannah, GA) featured RenovoRx's findings on real-time intra-arterial pressure monitoring during TAMP procedures using RenovoCath. The conference spotlighted pain palliation, pressure monitoring, and technological innovation.
- El Camino Hospital (Mountain View, CA)minorRenovoRx's CMO and Founder Dr. Ramtin Agah is an Interventional Cardiologist at El Camino Hospital, Mountain View, a role he has held since September 2005. This affiliation provides clinical expertise and proximity to RenovoRx's Mountain View headquarters.
- Abbott VascularminorDr. Ramtin Agah has acted as a physician consultant for Abbott Vascular since July 2012. This is a personal consulting arrangement of the CMO and does not represent a corporate partnership between RenovoRx and Abbott Vascular.
- Moffitt Cancer CenterflagshipMoffitt Cancer Center is a key clinical research partner. Dr. Bela Kis, MD, PhD and colleagues authored the peer-reviewed case study published in Radiology Case Reports (June 2026) demonstrating 52% reduction in tumor metabolic activity with TAMP/RenovoCath treatment. Dr. Mustafa Al-Roubaie, MD serves on RenovoRx's Medical Advisory Board. Clinical data abstracts from Moffitt experts have been presented at SIR 2026 and other major meetings.
- Scientific Advisory Board (Pancreatic Cancer and GI Oncology Experts)flagshipScientific Advisory Board comprises leading pancreatic cancer and GI oncology experts: Timothy Donahue, MD (UCLA), Michel Ducreux, MD, PhD (Gustave Roussy/Paris-Saclay), Karyn A. Goodman, MD, MS (Mount Sinai), Mike Pishvaian, MD, PhD (Johns Hopkins), Margaret Tempero, MD (UCSF), and previously added Dr. Thierry de Baère (international interventional oncologist). Board provides scientific guidance on TAMP platform and RenovoCath clinical development.
- Artelo BiosciencesminorPer March 23, 2026 defenseworld article, RenovoRx (NASDAQ: RNXT) and Artelo Biosciences (NASDAQ: ARTL) are small-cap medical companies compared based on earnings, risk, analyst ratings, and valuation. RenovoRx is viewed more favorably due to higher revenue, earnings, and stronger analyst recommendations. This is a competitive comparison, not a formal partnership.
Scale indicators11 records
Recent moves6 records
Expansion highlights8 records
RenovoRx competitors and assessment
Company assessmentDirect peers
- TriSalus Life Sciences: TriSalus develops the Pressure-Enabled Drug Delivery (PEDD) platform for intra-arterial delivery of therapeutics to solid tumors, including pancreatic cancer via the Limbus portal vein approach. Both companies are pursuing locally advanced pancreatic cancer with interventional oncology drug-delivery devices.
- AngioDynamics: AngioDynamics markets interventional oncology and vascular access products, including the NanoKnife irreversible electroporation system for pancreatic and other tumors. Comparable as a similarly sized public medtech focused on interventional oncology devices.
- Sirtex Medical: Sirtex develops SIR-Spheres Y-90 resin microspheres for intra-arterial radioembolization of liver tumors — a directly analogous intra-arterial, targeted-delivery oncology device. Comparable mechanism of action (localized intra-arterial therapy) and indication profile.
- DELcath Systems: DELcath develops the Melphalan/Hepatic Delivery System (CHEMOSAT) for percutaneous hepatic perfusion of liver tumors — an organ-targeted, intra-arterial drug-delivery device. Comparable as a small-cap public interventional oncology drug-device combination company.
Broad incumbents
- Boston Scientific: Boston Scientific is a major interventional oncology and peripheral vascular device incumbent and is also a RenovoRx historical investor. Comparable as a broad incumbent with overlapping interventional radiology portfolios and significantly greater scale.
- Merit Medical Systems: Merit Medical offers a broad portfolio of interventional radiology and oncology products, including embolization and drug-delivery catheters that compete in the same interventional oncology procedure suites where RenovoCath is sold.
- Penumbra: Penumbra is a publicly traded vascular and interventional thrombectomy/embolization company with overlapping call points in interventional radiology suites treating solid tumors. Comparable as a peripheral vascular interventional device incumbent.
- Medtronic: Medtronic operates a large interventional oncology and vascular franchise. RenovoRx's CEO previously led the European launch of Medtronic-acquired Ardian's renal denervation technology, and the broader Medtronic portfolio overlaps in peripheral vascular interventional devices.
Emerging players
- IceCure Medical: IceCure is a small-cap public company developing cryoablation technologies for tumor treatment, including breast and other solid tumors. Comparable as a small-cap interventional oncology device company pursuing novel localized tumor therapies.
- Taris Biomedical (a subsidiary of Bristol Myers Squibb): Taris developed intravesical drug-delivery systems for bladder cancer and was acquired by BMS. Comparable as an intra-arterial / local drug-delivery oncology platform with an exit via a major pharma acquirer — relevant precedent for RenovoRx's combination-product strategy.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat6 records
Key risks6 records
Key highlights7 records
Customer concentration
RenovoRx social profiles
Digital presenceRenovoRx financial estimates
Financial estimateRevenue estimate
Valuation estimate
RenovoRx leadership team
Management profileNumber of profiles
Profiles11 records
RenovoRx funding detail
Funding detailFunding overview
Funding rounds11 records
Investors10 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
RenovoRx M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about RenovoRx
What does RenovoRx do?
RenovoRx develops and commercializes the FDA 510(k)-cleared RenovoCath dual-balloon catheter device and its proprietary Trans-Arterial Micro-Perfusion (TAMP) therapy platform for targeted intra-arterial delivery of chemotherapy to treat solid tumors. The company sells RenovoCath as a stand-alone medical device to U.S. cancer centers and is advancing the investigational drug-device combination IAG (intra-arterial gemcitabine) through the Phase III TIGeR-PaC clinical trial for locally advanced pancreatic cancer.
Is RenovoRx a public or private company?
RenovoRx is a public company. It is classified as public and is currently operating.
When was RenovoRx founded?
RenovoRx was founded in 2009. It employs 11 to 50 people.
Where is RenovoRx based?
RenovoRx is headquartered in Mountain View, United States, in the North America region.
How does RenovoRx make money?
Three revenue lines are on record. RenovoCath Device Sales are the primary driver. The others are future Drug-Device Combination Revenue (IAG) and post-Marketing Registry Study Revenue Pathway.
Who are RenovoRx's main competitors?
Direct peers on record are TriSalus Life Sciences, AngioDynamics, Sirtex Medical and DELcath Systems. Broad incumbents are Boston Scientific, Merit Medical Systems, Penumbra and Medtronic. Emerging players are IceCure Medical and Taris Biomedical (a subsidiary of Bristol Myers Squibb).
Does RenovoRx have an API?
No public API is recorded for RenovoRx.
What industry is RenovoRx in?
RenovoRx's product category is Oncology Medical Devices. Its primary akta.pro industry code is HLAKAFAK, Gastrointestinal Oncology, with a secondary code of HLAIAAAM, Nephrology & Urology Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 3841.