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RenovoRx

Full company profile

uuid000075z

Namestring
RenovoRx
Legal namestring
RenovoRx, Inc.
Websiteurl
renovorx.com
Company typeenum
Public
Founded yearint
2009
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersMountain View, United States
HQ citystring
Mountain View
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
targeted drug delivery, oncology medical devices, intra-arterial chemotherapy, trans-arterial micro-perfusion, dual-balloon catheter
Industry3 codes
1Gastrointestinal Oncology
CodeHLAKAFAKPrimaryYes
2Nephrology & Urology Pharmaceuticals
CodeHLAIAAAMPrimaryNo
3DTx/SaMD Deployment, Integration & Reimbursement Enablement
CodeHLACANAOPrimaryNo
NAICS code2 codes
  • Pharmaceutical Preparation Manufacturing325412
  • In-Vitro Diagnostic Substance Manufacturing325413
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Oncology Medical Devices
Social media profiles3 records
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1RenovoCath Device Sales
TypeHardware Sales
Description

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.

renovorx.com
2Future Drug-Device Combination Revenue (IAG)
TypeHardware Sales
Description

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.

renovorx.com
3Post-Marketing Registry Study Revenue Pathway
TypeProfessional Services
Description

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.

biospace.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Marketing or Sales, Operations
Pricing details1 tier
1Quote-based / not publicly disclosed; revenue is generated per device sold and per procedure performed at cancer centers
ModelOtherBilling cadencePay-as-you-go
Notes

No public price list. Device is sold under prescription only. Reimbursement dynamics drive organic growth. 2024 revenue was $43,000; Q4 2025 revenue was $238,000; Full year 2025 revenue was $1.1 million; Q1 2026 revenue was $563,000. Full year 2026 revenue guidance of $3-4 million reiterated.

renovorx.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1RenovoCath
Description

FDA-cleared dual-balloon drug-delivery device for targeted local delivery of chemotherapy

globenewswire.com
+2 more records
Core offering1 text field

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.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • 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 records
Product overview1 text field

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).

Product and service2 records
1RenovoCath Dual-Balloon Occlusion Catheter
CategoryMedical Device / Drug Delivery Catheter
Description

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.

2IAG (Intra-Arterial Gemcitabine) Drug-Device Combination
CategoryInvestigational Drug-Device Combination
Description

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).

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership15 partners
Strategic tierMinorTypeGTM or Marketing PartnerAnnounced on2026-05-20
Description

Hosted 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.

2U.S. Interventional Radiology Experts (RenovoCath Medical Advisory Board)
Strategic tierFlagshipTypeOthersAnnounced on2026-02-10
Description

RenovoRx 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.

stocktitan.net
Strategic tierMinorTypeGTM or Marketing PartnerAnnounced on2026-01-16
Description

Investor 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.

Strategic tierMinorTypeGTM or Marketing PartnerAnnounced on2025-12-09
Description

Investor 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.

Strategic tierMinorTypeGTM or Marketing PartnerAnnounced on2025-11-20
Description

Forum held November 20, 2025, where CEO Shaun Bagai discussed RenovoRx's clinical progress and market demand for the RenovoCath device.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

RenovoRx'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.

Strategic tierCoreTypeGTM or Marketing Partner
Description

RenovoRx's media relations partner. Contact: Hannah Williams, T: 803-521-1214, [email protected]. Listed as Media Contact on press releases.

Strategic tierCoreTypeGTM or Marketing Partner
Description

RenovoRx 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.

Strategic tierCoreTypeGTM or Marketing Partner
Description

RenovoRx 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.

Strategic tierCoreTypeGTM or Marketing Partner
Description

RenovoRx 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.

Strategic tierMinorTypeOthers
Description

RenovoRx'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.

Strategic tierMinorTypeOthers
Description

Dr. 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.

Strategic tierFlagshipTypeStrategic or Co-development Partner
Description

Moffitt 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.

14Scientific Advisory Board (Pancreatic Cancer and GI Oncology Experts)
Strategic tierFlagshipTypeOthers
Description

Scientific 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.

renovorx.com
Strategic tierMinorTypeOthers
Description

Per 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.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight8 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeEmerging player
Description

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.

TypeEmerging player
Description

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.

TypeDirect peer
Description

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.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers17 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration1 record

Each record includes

Title, Type, Description, Source

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds11 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors10 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

RenovoRx

Oncology Medical Devicesrenovorx.com

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.

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

  • Targeted drug delivery
  • Oncology medical devices
  • Intra-arterial chemotherapy
  • Trans-arterial micro-perfusion
  • Dual-balloon catheter

Where RenovoRx is headquartered

Location

Headquarters

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

  1. 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.
  2. 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.
  3. 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

ModelBillingPrice
OtherPay-as-you-goQuote-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 offering

Core 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 profile

Named customers17 records

Segments2 records

Ideal customer profiles2 records

RenovoRx technology and API

Technology

Technology 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 signal

Partnerships

15 partnerships are on record, tiered minor, flagship and core.

  • Alliance Global Partners (AGP)minorGTM or Marketing Partner · 20 May 2026Hosted 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)flagshipOthers · 10 February 2026RenovoRx 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 EventminorGTM or Marketing Partner · 16 January 2026Investor 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 AlphaminorGTM or Marketing Partner · 9 December 2025Investor 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 ForumminorGTM or Marketing Partner · 20 November 2025Forum held November 20, 2025, where CEO Shaun Bagai discussed RenovoRx's clinical progress and market demand for the RenovoCath device.
  • KCSA Strategic CommunicationscoreStrategic or Co-development PartnerRenovoRx'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 CommunicationscoreGTM or Marketing PartnerRenovoRx'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)coreGTM or Marketing PartnerRenovoRx 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)coreGTM or Marketing PartnerRenovoRx 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)coreGTM or Marketing PartnerRenovoRx 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)minorOthersRenovoRx'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 VascularminorOthersDr. 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 CenterflagshipStrategic or Co-development PartnerMoffitt 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)flagshipOthersScientific 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 BiosciencesminorOthersPer 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 assessment

Direct 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 presence

RenovoRx financial estimates

Financial estimate

Revenue estimate

Valuation estimate

RenovoRx leadership team

Management profile

Number of profiles

Profiles11 records

RenovoRx funding detail

Funding detail

Funding 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 investment

M&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.

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Simply Wall StHere's Why We're Watching RenovoRx's (NASDAQ:RNXT) Cash Burn SituationRenovoRx's cash burn increased 16% to $12m last year, leaving a 10-month runway from its $9.5m cash balance. Analysts forecast breakeven in about 21 months, so the company may need to raise cash. The burn relative to its $66m market cap is 18%.American Banking and Market NewsReviewing Omnicell (NASDAQ:OMCL) & RenovoRx (NASDAQ:RNXT)Omnicell and RenovoRx are compared on analyst ratings, institutional ownership, and valuation. RenovoRx shows higher upside (511.51% vs 63.16%) and lower P/E, but Omnicell beats on 10 of 14 factors. RenovoRx's lead product is in Phase III trials for pancreatic cancer.American Banking and Market NewsMedline (NASDAQ:MDLN) versus RenovoRx (NASDAQ:RNXT) Head-To-Head ComparisonMedline and RenovoRx are compared on analyst ratings, valuation, and profitability. Medline has higher revenue and earnings, while RenovoRx shows higher upside potential. Medline beats RenovoRx on 10 of 14 factors.Markets DailyRenovoRx, Inc. (NASDAQ:RNXT) Sees Large Growth in Short InterestShort interest in RenovoRx rose 55.7% to 673,558 shares as of September 15th. Analysts' ratings shifted, with Weiss Ratings raising from sell to sell (d-) and Wall Street Zen from sell to hold. The stock opened at $1.58, with a consensus target of $8.50.Ticker ReportBioventus (NASDAQ:BVS) vs. RenovoRx (NASDAQ:RNXT) Head-To-Head ReviewBioventus and RenovoRx are compared on revenue, earnings, and analyst ratings. Bioventus has higher revenue ($581.85M vs $1.12M) and profitability, while RenovoRx shows higher potential upside (412% vs 21.65%). Bioventus beats RenovoRx on 11 of 15 factors.AdvfnRenovoRx H.C. Wainwright Presentation to Highlight RenovoCath Growth and Phase III TIGeR-PaC TimelineRenovoRx will present at H.C. Wainwright on September 14, covering RenovoCath commercial growth and Phase III TIGeR-PaC data. The company reported $1.1 million in RenovoCath sales in 2025 and $909,000 in Q2 2026, with the Phase III trial completing in early 2027 and topline results expected in the second half.BioSpaceRenovoRx to Present at H.C. Wainwright 28th Annual Global Investment Conference, September 14th-16thRenovoRx CEO Shaun Bagai and CFO Mark Voll will present at the H.C. Wainwright 28th Annual Global Investment Conference in New York City on September 14-16, 2026. They will discuss record Q2 revenue of $909,000 and the first clinical use of RenovoCath in a sarcoma patient. The company will also update on the fully enrolled Phase III TIGeR-PaC trial, with completion expected in the first half of 2027.AInvestRenovoRx's New Paper Proves the Delivery Mechanism. The 17% Rally Prices a Survival Verdict Still a Year AwayRenovoRx's shares rose about 17% to roughly $1.46, valuing the company at about $70 million, after peer-reviewed data showed its intra-arterial gemcitabine platform extracts roughly 51% of the drug at the tumor site. The 16-patient sub-study was already presented at ASCO GI in January 2026. A 114-patient pancreatic cancer trial, with 78 of 86 required events accrued, is guided to a second-half 2027 readout.BioSpaceRenovoRx Highlights Peer-Reviewed Publication of Pharmacokinetic and Pharmacodynamic (PK/PD) Data Supporting TAMP™ Platform’s Targeted Drug-Delivery in Locally Advanced Pancreatic CancerRenovoRx published PK/PD data from a sub-study of its Phase III TIGeR-PaC trial in Cancer Chemotherapy and Pharmacology. The data showed approximately 51% tumor-site drug extraction and a significant correlation between drug metabolite levels and CA 19-9 reduction. Trial completion is expected in the first half of 2027.BioSpaceRenovoRx Regains Compliance with Nasdaq Minimum Bid Price RequirementRenovoRx regained compliance with Nasdaq's minimum bid price requirement, confirmed by Nasdaq on August 20, 2026, after 10 consecutive business days of closing bid prices at or above $1.00 per share. The company reported record second-quarter revenue of $909,000 and is advancing its Phase III TIGeR-PaC trial, with data readout expected in the second half of 2027.