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RenovoRx Reports Initial Revenues from RenovoCath® Commercialization, and Provides Update on Ongoing Pivotal Phase III TIGeR-PaC Clinical Trial

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RenovoRx (RNXT) has reported its first commercial revenue of $43,000 in Q4 2024 from RenovoCath® device sales, marking a significant milestone. The company projects sequential revenue growth into 2025, targeting a low six-figure range for Q1. RenovoCath's initial total addressable market is estimated at $400 million in peak annual U.S. sales, with potential expansion to several billion dollars across other indications.

The company's Phase III TIGeR-PaC clinical trial has enrolled 90 patients with 50 events recorded as of March 28, 2025. A second interim analysis is expected in Q2 2025 upon reaching 52 events. The company maintains a strong financial position with $7.2 million cash as of December 31, 2024, supplemented by an additional $12.1 million raised in February 2025.

Financial results show R&D expenses of $6.0 million and SG&A expenses of $5.0 million for 2024. Net loss improved to $8.8 million compared to $10.2 million in 2023.

RenovoRx (RNXT) ha riportato il suo primo fatturato commerciale di $43.000 nel quarto trimestre del 2024 dalle vendite del dispositivo RenovoCath®, segnando un traguardo significativo. L'azienda prevede una crescita sequenziale del fatturato nel 2025, puntando a un intervallo di sei cifre basse per il primo trimestre. Il mercato totale indirizzabile iniziale di RenovoCath è stimato in $400 milioni nelle vendite annuali di picco negli Stati Uniti, con una potenziale espansione a diversi miliardi di dollari in altre indicazioni.

Il trial clinico di Fase III TIGeR-PaC dell'azienda ha arruolato 90 pazienti con 50 eventi registrati al 28 marzo 2025. Un'analisi intermedia secondaria è prevista nel secondo trimestre del 2025 al raggiungimento di 52 eventi. L'azienda mantiene una solida posizione finanziaria con $7,2 milioni in contante al 31 dicembre 2024, integrata da ulteriori $12,1 milioni raccolti a febbraio 2025.

I risultati finanziari mostrano spese per R&S di $6,0 milioni e spese SG&A di $5,0 milioni per il 2024. La perdita netta è migliorata a $8,8 milioni rispetto ai $10,2 milioni del 2023.

RenovoRx (RNXT) ha reportado sus primeros ingresos comerciales de $43,000 en el cuarto trimestre de 2024 por las ventas del dispositivo RenovoCath®, marcando un hito significativo. La compañía proyecta un crecimiento secuencial de ingresos hacia 2025, apuntando a un rango de seis cifras bajas para el primer trimestre. El mercado total direccionable inicial de RenovoCath se estima en $400 millones en ventas anuales pico en EE. UU., con una posible expansión a varios miles de millones de dólares en otras indicaciones.

El ensayo clínico de Fase III TIGeR-PaC de la compañía ha inscrito a 90 pacientes con 50 eventos registrados hasta el 28 de marzo de 2025. Se espera un segundo análisis intermedio en el segundo trimestre de 2025 al alcanzar 52 eventos. La compañía mantiene una sólida posición financiera con $7.2 millones en efectivo al 31 de diciembre de 2024, complementada por $12.1 millones adicionales recaudados en febrero de 2025.

Los resultados financieros muestran gastos de I+D de $6.0 millones y gastos SG&A de $5.0 millones para 2024. La pérdida neta mejoró a $8.8 millones en comparación con $10.2 millones en 2023.

RenovoRx (RNXT)는 2024년 4분기 RenovoCath® 장치 판매로 $43,000의 첫 상업 수익을 보고하며 중요한 이정표를 세웠습니다. 이 회사는 2025년으로의 순차적 수익 성장을 예상하며, 1분기에는 낮은 6자리 수익을 목표로 하고 있습니다. RenovoCath의 초기 총 주소able 시장은 미국에서의 연간 최대 판매액이 $400백만으로 추정됩니다, 다른 적응증에서 수십억 달러로 확장될 가능성이 있습니다.

회사의 3상 TIGeR-PaC 임상 시험에는 2025년 3월 28일 기준으로 90명의 환자가 등록되었으며 50개의 사건이 기록되었습니다. 52개의 사건에 도달하면 2025년 2분기에 두 번째 중간 분석이 예상됩니다. 회사는 2024년 12월 31일 기준으로 $7.2 백만의 현금을 보유하고 있으며, 2025년 2월에 추가로 $12.1 백만을 모금했습니다.

재무 결과는 2024년 연구개발(R&D) 비용이 $6.0 백만, 판매 및 일반 관리(SG&A) 비용이 $5.0 백만임을 보여줍니다. 순손실은 2023년의 $10.2 백만에 비해 $8.8 백만으로 개선되었습니다.

RenovoRx (RNXT) a rapporté son premier revenu commercial de 43 000 $ au quatrième trimestre 2024 grâce aux ventes du dispositif RenovoCath®, marquant une étape importante. L'entreprise projette une croissance séquentielle des revenus pour 2025, visant une fourchette basse à six chiffres pour le premier trimestre. Le marché total adressable initial de RenovoCath est estimé à 400 millions de dollars en ventes annuelles maximales aux États-Unis, avec une expansion potentielle à plusieurs milliards de dollars dans d'autres indications.

Le essai clinique de Phase III TIGeR-PaC de l'entreprise a recruté 90 patients avec 50 événements enregistrés au 28 mars 2025. Une seconde analyse intermédiaire est attendue au deuxième trimestre 2025 après avoir atteint 52 événements. L'entreprise maintient une solide position financière avec 7,2 millions de dollars en espèces au 31 décembre 2024, complétée par 12,1 millions de dollars supplémentaires levés en février 2025.

Les résultats financiers montrent des dépenses de R&D de 6,0 millions de dollars et des dépenses SG&A de 5,0 millions de dollars pour 2024. La perte nette s'est améliorée à 8,8 millions de dollars par rapport à 10,2 millions de dollars en 2023.

RenovoRx (RNXT) hat im vierten Quartal 2024 einen ersten kommerziellen Umsatz von $43.000 aus dem Verkauf des RenovoCath®-Geräts gemeldet, was einen bedeutenden Meilenstein darstellt. Das Unternehmen prognostiziert ein sequenzielles Umsatzwachstum bis 2025 und strebt für das erste Quartal einen niedrigen sechsstelligen Betrag an. Der anfängliche insgesamt adressierbare Markt von RenovoCath wird auf $400 Millionen bei den jährlichen Höchstverkäufen in den USA geschätzt, mit einer potenziellen Erweiterung auf mehrere Milliarden Dollar in anderen Indikationen.

Die Phase-III-TIGeR-PaC-Studie des Unternehmens hat 90 Patienten eingeschlossen, wobei bis zum 28. März 2025 50 Ereignisse registriert wurden. Eine zweite Zwischenanalyse wird im 2. Quartal 2025 erwartet, sobald 52 Ereignisse erreicht sind. Das Unternehmen hat eine starke finanzielle Position mit $7,2 Millionen in bar zum 31. Dezember 2024, ergänzt durch zusätzlich $12,1 Millionen, die im Februar 2025 gesammelt wurden.

Die finanziellen Ergebnisse zeigen F&E-Ausgaben von $6,0 Millionen und SG&A-Ausgaben von $5,0 Millionen für 2024. Der Nettoverlust verbesserte sich auf $8,8 Millionen im Vergleich zu $10,2 Millionen im Jahr 2023.

Positive
  • First commercial revenue achieved with $43,000 in Q4 2024
  • Strong cash position of $19.3 million following February 2025 offering
  • Reduced net loss to $8.8 million in 2024 from $10.2 million in 2023
  • Multiple purchase orders from NCI-designated centers with repeat orders
  • Existing reimbursement code with CMS covering RenovoCath procedures
Negative
  • Operating loss of $11 million in 2024
  • R&D expenses increased by $0.3 million to $6.0 million in 2024
  • Initial revenue of $43,000 represents minimal market penetration
  • Phase III trial enrollment not yet complete with 24 more patients needed

Insights

RenovoRx has reached a pivotal inflection point with its first commercial revenues of $43,000 from RenovoCath in Q4 2024. Their projection of low six-figure revenue for Q1 2025 with sequential quarterly growth signals the beginning of their commercial phase, though from an extremely modest base.

The company's financial position appears stable for near-term operations with $7.2 million cash at year-end plus $12.1 million in gross proceeds raised in February 2025. This $19.3 million cash position should provide adequate runway as management expects RenovoCath revenues to help reduce their burn rate, which was approximately $8.8 million in 2024.

The TIGeR-PaC trial is progressing with 90 patients randomized (out of the required 114) and 50 events recorded (toward the 86 needed). The upcoming second interim analysis, triggered at the 52nd event (expected Q2 2025), represents a critical milestone that could significantly impact the company's trajectory.

While management's stated $400 million peak annual U.S. sales opportunity for RenovoCath represents substantial potential upside, investors should view this projection cautiously given the typical challenges in achieving meaningful market penetration in specialized medical device segments.

The reduction in net loss from $10.2 million in 2023 to $8.8 million in 2024 shows improved operational efficiency, though the company remains heavily in investment mode with R&D expenses of $6 million representing a significant portion of expenditures.

RenovoRx's Trans-Arterial Micro-Perfusion (TAMP) platform represents an innovative approach to targeted oncology therapy, with the initial commercial traction offering preliminary validation. The receipt of purchase orders from NCI-designated centers is particularly noteworthy, as these institutions typically maintain rigorous standards for adopting new technologies.

The repeat orders from initial customers suggest clinical utility and potential product-market fit, though the small revenue base ($43,000) indicates we're still in the very early adoption phase. The existing reimbursement code for pressure-mediated delivery catheters removes a significant barrier to hospital adoption, as facilities won't face additional administrative hurdles to recoup costs.

The TIGeR-PaC trial's progression is critical for long-term success. With 90 patients randomized and 50 events recorded, the impending second interim analysis will provide crucial data on efficacy. The Data Monitoring Committee's recommendation expected in H2 2025 will be a decisive moment that could accelerate or hinder broader clinical acceptance.

From a technical perspective, RenovoRx's intellectual property portfolio (18 issued patents, 13 pending) provides reasonable protection for their TAMP platform. The presentation of additional human pharmacokinetic data and pre-clinical results at major oncology conferences indicates ongoing validation of the technology's scientific foundation.

Their commercial strategy targeting 200 high-volume treatment centers with a small team appears reasonably efficient, though the company will likely face challenges in driving consistent utilization beyond initial procedural trials.

Revenues from RenovoCath Expected to Grow Sequentially During 2025 with Expansion of New Customer Purchase Orders and Customer Reorders

Completion of TIGeR-PaC Clinical Trial Enrollment and Review of Second Interim Analysis by Data Monitoring Committee on Target for 2025

Reports 2024 Financial Results Including $7.2 Million Cash Position as of December 31, 2024, with Additional $12.1 Million in Gross Proceeds Raised in February 2025

Company to Host Fireside Chat on Thursday, April 3rd at 12 p.m. ET

MOUNTAIN VIEW, Calif.--(BUSINESS WIRE)-- RenovoRx, Inc. (“RenovoRx” or the “Company”) (Nasdaq: RNXT), a life sciences company developing innovative targeted oncology therapies and commercializing RenovoCath®, a novel, FDA-cleared drug-delivery device, today announced its financial results and business updates for the fourth quarter and full year ended December 31, 2024.

“The fourth quarter of 2024 marks a significant milestone in our company history as we have generated our first revenue from sales of our proprietary RenovoCath device on a standalone basis, with expectations for meaningful revenue growth going forward. Importantly, we believe our current commercial strategy can be accomplished without a material increase in our capital expenditures, regardless of whether we self-commercialize or choose to partner with a larger organization and use their existing sales force and channels. Further, we believe that the gross proceeds from our February 2025 public offering of $12.1 million together with our cash on hand of $7.2 million at year end fully funds our current operational plan as we look to scale RenovoCath revenues and progress our Phase III TIGeR-PaC clinical trial towards key milestones. Moreover, we expect that growing RenovoCath revenues will reduce our burn rate as we prudently deploy our cash on hand to drive shareholder value,” said Shaun Bagai, CEO of RenovoRx.

“Based on our internal analysis with current clinical applications, we believe that our initial total addressable market (TAM) for RenovoCath represents an estimated $400 million peak annual U.S. sales opportunity. Beyond this, there are expansion opportunities across other indications that could create the potential for a several billion-dollar U.S. TAM for RenovoCath over time,” continued Mr. Bagai. “We expect revenue to increase to the low six figure range for the first quarter of 2025 followed by sequential quarter-over-quarter increases for the remainder of the year.”

RenovoCath Commercialization Update

In December 2024, RenovoRx received first commercial purchase orders for its RenovoCath device, which resulted in revenue generation of approximately $43,000 for the fourth quarter of 2024.

RenovoRx is seeing strong organic demand for RenovoCath. More than ten medical institutions have initiated the process for RenovoCath purchase orders, and purchase orders have already been received from several esteemed, high volume National Cancer Institute-designated centers. Additionally, utilization of RenovoCath devices by initial customers has led to repeat purchase orders. Moreover, RenovoRx believes the twenty cancer centers that have used RenovoCath as part of its TIGeR-PaC trial could also be potential customers for RenovoCath after completion of TIGeR-PaC enrollment later this year.

RenovoRx has identified its initial target market for RenovoCath to be approximately $400 million in peak annual U.S. sales, based on the Company’s internal assumptions1. Moreover, expansion opportunities across other clinical indications could create a several billion-dollar total addressable market potential for RenovoCath over time. It’s management’s belief that the Company can achieve meaningful market penetration with a small commercial team targeting the top 200 high-volume treatment centers.

Importantly, there is a current reimbursement code with the Centers for Medicare and Medicaid Services covering procedures utilizing specialty pressure-mediated delivery catheters, which creates incentives for hospitals to adopt more advanced technology, like RenovoCath.

Ongoing Pivotal Phase III TIGeR-PaC Clinical Trial Update

During the fourth quarter 2024, RenovoRx added several additional renowned clinical oncology sites to participate in the TIGeR-PaC study. The initiation of these sites allows for new patient enrollment at the Sarah Cannon Research Institute Oncology Partners in Nashville, TN and at the Northwell Health Cancer Institute Clinical Site in New Hyde Park, NY which are key additions to the number of clinical sites to support RenovoRx’s path to completing patient enrollment for the trial. RenovoRx is continuing to target additional clinical oncology sites, with the expectation that the study will achieve full enrollment during 2025.

The current protocol and statistical analysis plan for the TIGeR-PaC trial requires 114 randomized patients, with 86 events (deaths) necessary to complete the final analysis. As of March 28, 2025, 90 patients have been randomized with 50 events having occurred. A second interim analysis will be triggered by the 52nd event.

The timing required to analyze the data after the 52nd event is expected to take several months and includes a full review with recommendations by the TIGeR-PaC Data Monitoring Committee. RenovoRx currently anticipates the 52nd event to occur during the second quarter of 2025. The key recommendation from the Data Monitoring Committee on whether or not to continue the study based on the data reviewed is expected to be announced in the second half of 2025.

Fireside Chat Strategic Update

RenovoRx will host a fireside chat with Shaun Bagai, Chief Executive Officer, on Thursday, April 3, 2025, at 12:00 p.m. ET. During the event, Mr. Bagai will discuss the momentum of RenovoRx’s commercialization efforts for its RenovoCath device, including an update on initial revenues generated, and continued progress on the ongoing Phase III TIGeR-PaC clinical trial. Additionally, one of RenovoCath’s initial customers, Gregory Tiesi, MD, FACS, FSSO, Medical Director of Hepatobiliary Surgery, Division of Surgical Oncology, Hackensack Meridian Jersey Shore University Medical Center, will join Mr. Bagai. He will share his insights on the Trans-Arterial Micro-Perfusion (TAMP™) therapy platform and its impact on patient care. Hackensack Meridian Jersey Shore University Medical Center began using the RenovoCath device with oncology patients in December 2024.

Fireside Chat Details:
Date: Thursday, April 3, 2025
Time: 12:00 p.m. ET
Webcast: https://ir.renovorx.com/news-events/ir-calendar-events

A question and answer session will occur at the end of the call, and a link to the recording of this presentation will be available on RenovoRx’s Investor Relations website after the event.

____________________

1 Assumptions: (i) pressure-mediated delivery catheters on market today, which are analogous to RenovoCath, have an average selling price of $6,500-$8,500 per unit; (ii) approximately 7,000 initial target patients at peak market penetration; and (iii) an average of approximately 8 annual procedures per patient.

Additional Key Fourth Quarter 2024 and Subsequent Highlights

During the fourth quarter, RenovoRx expanded its Intellectual property Portfolio to include 18 issued patents and 13 pending patents for the novel TAMP therapy platform. In addition, during and subsequent to the fourth quarter, RenovoRx presented abstracts at the ASCO Gastrointestinal Cancers Symposium 2025, the Society of Interventional Oncology 2025, and the Society of Surgical Oncology 2025 supporting the TAMP therapy platform via additional human pharmacokinetic (PK) data and pre-clinical data. Additionally, a publication supporting TAMP for targeted locoregional drug delivery will be recognized in the Journal of Vascular and Interventional Radiology Award-Winning Paper Scientific Session during the upcoming the Society of Interventional Radiology 2025.

Financial Highlights for the Year Ended December 31, 2024

  • Revenue: Beginning December 2024, RenovoRx reported initial revenues of approximately $43,000 through sales of RenovoCath devices on a standalone basis directly to end users.
  • Cash Position: Cash and cash equivalents as of December 31, 2024, were $7.2 million, with an additional $12.1 million in gross ($10.9 million in net) proceeds raised in a common stock only public offering in February 2025.
  • R&D Expenses: Research and development expenses were $6.0 million for the year ended December 31, 2024, compared to $5.7 million for the year ended December 31, 2023, an increase of $0.3 million. This increase in research and development expenses is due to an increase in manufacturing and non-recurring engineering costs to scale manufacturing to support the commercial effort on our RenovoCath delivery system of $0.3 million and other research development expenses including personnel expenses for employees and benefits of $0.3 million. This increase was offset by a decrease in clinical development and regulatory costs of $0.3 million.
  • SG&A Expenses: Selling, general, and administrative expenses were $5.0 million for the year ended December 31, 2024, compared to $5.7 million for the year ended December 31, 2023, a decrease of $0.7 million. The decrease in selling, general, and administrative expenses was due to lower professional and consulting costs, including directors and officers’ insurance and legal fees of $0.9 million. This decrease was offset by an increase in personnel expenses for employees and benefits of $0.2 million, which is primarily due to an increase in employee incentive compensation.
  • Net Loss: Net loss was $8.8 million for the year ended December 31, 2024, compared to net loss of $10.2 million for the year ended December 31, 2023.
  • Shares Outstanding: Shares of common stock outstanding as of March 25, 2025, were 36,546,752.
RenovoRx, Inc.
Selected Balance Sheet Data
(in thousands)
December 31,

 

2024

 

 

2023

 

 
 
Cash and cash equivalents

$

7,154

 

$

1,173

 

Total assets

$

8,118

 

$

1,466

 

 
Total liabilities

$

3,640

 

$

4,466

 

Total stockholders' equity (deficit)

$

4,478

 

$

(3,000

)

Total liabilities and stockholders' equity (deficit)

$

8,118

 

$

1,466

 

 
 
RenovoRx, Inc.
Selected Statement of Operations Data
(in thousands, except for share and per share amount)
Year Ended
December 31,

 

2024

 

 

2023

 

 
Revenues

$

43

 

$

-

 

 
Operating expenses:
Research and development

 

6,025

 

 

5,667

 

Selling, general and administrative

 

4,988

 

 

5,729

 

Total Operating expenses

 

11,013

 

 

11,396

 

Loss from operations

 

(10,970

)

 

(11,396

)

Change in fair value of warrant liability

 

1,772

 

 

1,709

 

Interest income (expense), net

 

384

 

 

108

 

Financing costs allocated to warrant

 

-

 

 

(653

)

Total other income (expense), net

 

2,156

 

 

1,164

 

Net loss

$

(8,814

)

$

(10,232

)

 
Net loss per share, basic and diluted

$

(0.40

)

$

(0.99

)

 
Weighted-average shares of common stock outstanding, basic and diluted

 

22,271,163

 

 

10,290,667

 

Additional information regarding RenovoRx’s business and results of operations for 2024 can be found in its Annual Report on Form 10-K for the fiscal year ended December 31, 2024, which was filed with the SEC on March 31, 2025.

About RenovoCath

Based on its FDA clearance, RenovoCath® is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system. RenovoCath is also indicated for temporary vessel occlusion in applications including arteriography, preoperative occlusion, and chemotherapeutic drug infusion. For further information regarding our RenovoCath Instructions for Use (“IFU”), please see: IFU-10004-Rev.-F-Universal-IFU.pdf.

About the TIGeR-PaC Clinical Trial

TIGeR-PaC is an ongoing Phase III randomized multi-center study evaluating the proprietary TAMP™ (Trans-Arterial Micro-Perfusion) therapy platform for the treatment of LAPC. RenovoRx’s first investigational drug-device combination product candidate using the TAMP therapy platform enabled with the Company’s FDA-cleared RenovoCath® device for the intra-arterial administration of chemotherapy, gemcitabine (IAG).

About RenovoRx, Inc.

RenovoRx, Inc. (Nasdaq: RNXT) is a life sciences company developing innovative targeted oncology therapies and commercializing RenovoCath®, a novel, U.S. Food and Drug Administration (FDA)-cleared local drug delivery device, targeting high unmet medical needs. RenovoRx’s patented Trans-Arterial Micro-Perfusion (TAMP™) therapy platform is designed to ensure targeted therapeutic delivery across the arterial wall near the tumor site to bathe the target tumor, while potentially minimizing a therapy’s toxicities versus systemic intravenous therapy. RenovoRx’s novel approach to targeted treatment offers the potential for increased safety, tolerance, and improved efficacy, and its mission is to transform the lives of cancer patients by providing innovative solutions to enable targeted delivery of diagnostic and therapeutic agents.

In addition to the RenovoCath device, RenovoRx is also evaluating our novel Phase III drug-device combination oncology product candidate (intra-arterial gemcitabine, known as IAG). IAG is being evaluated under a U.S. investigational new drug application that is regulated by the FDA’s 21 CFR 312 pathway. The investigational IAG utilizes RenovoCath, the Company’s FDA-cleared drug-delivery device, indicated for temporary vessel occlusion in applications including arteriography, preoperative occlusion, and chemotherapeutic drug infusion. The combination of intra-arterial infusion of chemotherapy, gemcitabine, and the RenovoCath device is currently being evaluated for the treatment of LAPC by the Center for Drug Evaluation and Research (the drug division of FDA).

The combination product candidate, which is enabled the RenovoCath device, is currently under investigation and has not been approved for commercial sale. RenovoCath with gemcitabine received Orphan Drug Designation for pancreatic cancer and bile duct cancer, which provides 7 years of market exclusivity upon new drug application approval by the FDA.

RenovoRx is also engaged in implementing commercialization strategies utilizing its TAMP technology and FDA-cleared RenovoCath device as stand-alone device. In December 2024, RenovoRx announced the receipt of its first commercial purchase orders for RenovoCath devices. Additionally, certain of these customers have already initiated repeat orders as RenovoRx works to expand the number medical institutions that have initiated the process for RenovoCath purchase orders, including several esteemed, high volume National Cancer Institute-designated centers. To meet and satisfy the anticipated demand, RenovoRx will continue to actively explore further revenue-generating activity either on its own or in tandem with a medical device commercial partner.

For more information, visit www.renovorx.com. Follow RenovoRx on Facebook, LinkedIn, and X.

Cautionary Note Regarding Forward-Looking Statements

This press release and statements of the Company’s management made in connection therewith contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, and Section 21E of the Securities Exchange Act of 1934, including but not limited to statements regarding (i) our pre-clinical and clinical trials and studies, including the overall timing and timing for additional interim data readouts and timing for full enrollment for our ongoing TIGeR-PaC Phase III clinical trial study in LAPC, (ii) the potential of RenovoCath® or TAMP™ as standalone commercial products, our anticipated timing and levels of for revenue generation from RenovoCath sales, and our commercialization plans in general, (iii) the potential for our product candidates to treat or provide clinically meaningful outcomes for certain medical conditions or diseases and (iv) our efforts to explore commercialization strategies utilizing our TAMP technology. Statements that are not purely historical are forward-looking statements. The forward-looking statements contained herein are based upon our current expectations and beliefs regarding future events, many of which, by their nature, are inherently uncertain, outside of our control and involve assumptions that may never materialize or may prove to be incorrect. These may include estimates, projections and statements relating to our research and development plans, commercial plans, intellectual property development, clinical trials, our therapy platform, business plans, financing plans, objectives and expected operating results, which are based on current expectations and assumptions that are subject to significant known and unknown risks and uncertainties that may cause actual results to differ materially and adversely from those expressed or implied by these forward-looking statements. These statements may be identified using words such as “may,” “expects,” “plans,” “aims,” “anticipates,” “believes,” “forecasts,” “estimates,” “intends,” and “potential,” or the negative of these terms or other comparable terminology regarding RenovoRx’s expectations strategy, plans or intentions, although not all forward-looking statements contain these words. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, that could cause actual events to differ materially from those projected or indicated by such statements, including, among other things: (i) the risk that our execution of our commercial strategy for RenovoCath or our TAMP technology may not lead to viable or repeating revenue generating operations; (ii) circumstances which would adversely impact our ability to efficiently utilize our cash resources on hand or raise additional funding, (iii) the timing of the initiation, progress and potential results (including the results of interim analyses) of TIGeR-PaC and any other preclinical studies, clinical trials and our research programs; (iv) the possibility that interim results may not be predictive of the outcome of our clinical trials, which may not demonstrate sufficient safety and efficacy to support regulatory approval of our product candidate, (v) that the applicable regulatory authorities may disagree with our interpretation of the data; research and clinical development plans and timelines, and the regulatory process for our product candidates; (vi) future potential regulatory milestones for our product candidates, including those related to current and planned clinical studies; (vii) our ability to use and expand our therapy platform to build a pipeline of product candidates; (viii) our ability to advance product candidates into, and successfully complete, clinical trials; (ix) the timing or likelihood of regulatory filings and approvals; (x) our estimates of the number of patients who suffer from the diseases we are targeting and the number of patients that may enroll in our clinical trials; (xi) the commercialization potential of our product candidates, if approved; (xii) our ability and the potential to successfully manufacture and supply our product candidates for clinical trials and for commercial use, if approved; (xiii) future strategic arrangements and/or collaborations and the potential benefits of such arrangements; (xiv) our estimates regarding expenses, future revenue, capital requirements and needs for additional financing and our ability to obtain additional capital; (xv) the sufficiency of our existing cash and cash equivalents to fund our future operating expenses and capital expenditure requirements; (xvi) our ability to retain the continued service of our key personnel and to identify, and hire and retain additional qualified personnel; (xvii) the implementation of our strategic plans for our business and product candidates; (xviii) the scope of protection we are able to establish and maintain for intellectual property rights, including our therapy platform, product candidates and research programs; (xix) our ability to contract with third-party suppliers and manufacturers and their ability to perform adequately; (xx) the pricing, coverage and reimbursement of our product candidates, if approved; and (xxi) developments relating to our competitors and our industry, including competing product candidates and therapies. Information regarding the foregoing and additional risks may be found in the section entitled “Risk Factors” in documents that we file from time to time with the Securities and Exchange Commission.

Forward-looking statements included herein are made as of the date hereof, and RenovoRx does not undertake any obligation to update publicly such forward-looking statements to reflect subsequent events or circumstances, except as required by law.

KCSA Strategic Communications

Valter Pinto or Jack Perkins

T: 212-896-1254

RenovoRX@KCSA.com

Source: RenovoRx, Inc.

FAQ

What revenue did RNXT generate from RenovoCath sales in Q4 2024?

RenovoRx generated its first commercial revenue of $43,000 from RenovoCath device sales in Q4 2024.

What is the market potential for RenovoCath according to RNXT?

RenovoCath's initial total addressable market is estimated at $400 million in peak annual U.S. sales, with potential expansion to several billion dollars across other clinical indications.

What is the current status of RNXT's TIGeR-PaC Phase III trial?

As of March 28, 2025, 90 patients have been randomized with 50 events recorded. The trial requires 114 patients total, with a second interim analysis expected in Q2 2025.

How much cash does RNXT have available after the February 2025 offering?

RNXT has $7.2 million in cash as of December 31, 2024, plus $12.1 million raised in February 2025, totaling approximately $19.3 million.

What are RNXT's revenue projections for Q1 2025?

RNXT expects revenue to increase to the low six-figure range for Q1 2025, with sequential quarter-over-quarter increases throughout the year.
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