RenovoRx Reports Full Year 2022 Financial Results and Achievement of Important Phase III Clinical Study Milestone First of Two Planned Interim Analyses Triggered Company and Data Monitoring Committee Conducting Review Re

Reports Full Year 2022 Financial Results and Achievement of Important Phase III Clinical Study Milestone

of Two Planned Interim Analyses Triggered

and Data Monitoring Committee Conducting Review

of Analysis Forthcoming

Altos, CA, March 2, 2023 - RenovoRx, Inc. ("RenovoRx" or the "Company") (Nasdaq: RNXT), a biopharmaceutical

company focused on the localized treatment of solid tumors, today is reporting its financial results for the year ended December 31,

2022, and a pipeline update including the status of the interim analysis of for the Company's Phase III TIGeR-PaC clinical trial.

anticipates finalizing the interim analysis for the TIGeR-PaC Phase III trial and releasing the results within the next week or so. To

date, 47 out of 114 target post-SBRT/chemotherapy patients have been randomized in the TIGeR-PaC clinical trial, and the Company has

received reports of 26 events (deaths) in this population. This 26th event represents 30% of the 86 events and thus triggered

the first planned interim analysis and a meeting of the study's Data Monitoring Committee ("DMC") to evaluate the ongoing

progression of the Phase III clinical trial. Upon completion of the analysis and assessment of the data by the DMC, and RenovoRx's

subsequent review of their findings, the Company will report the first interim analysis.

is a randomized multi-center Phase III open label clinical trial designed to investigate the Company's first product candidate,

RenovoGemTM, which utilizes RenovoRx's proprietary therapy platform, RenovoTAMP , to provide targeted

intra-arterial delivery of FDA-approved chemotherapy, gemcitabine, to treat locally advanced pancreatic cancer (LAPC) following stereotactic

body radiation therapy (SBRT). The study is comparing treatment with RenovoTAMP versus standard of care systemic intravenous (IV) administration

of gemcitabine and nab-paclitaxel. The study is designed to randomize 114 patients (57 in each arm) with all patients receiving upfront

induction chemotherapy and SBRT. Final analysis will be conducted after 86 protocol-specified events have occurred in the SBRT population

with two planned interim analyses: the first analysis when 30% of the specified events have been reported (data announcement forthcoming)

and the second analysis when 60% of the events have been reported (expected in 2024).

continued to grow in 2022 as we have focused on advancing our innovative therapy platform with the vision of disrupting the current standard

of care," said Shaun Bagai, CEO of RenovoRx. "Over the past year, we have advanced our mission to transform oncology therapy

with our TIGeR-PaC Phase III study, treating pancreatic cancer, and expanding our clinical pipeline to treat other solid tumors. We have

also built a strong internal team, and we look forward to continued progress as we strive to give our patients not just more time but

more quality time that they can spend with their loved ones."

Year 2022 and Subsequent Operational Highlights:

Highlights for the Fiscal Year Ended December 31, 2022

is the first drug-device combination product candidate that utilizes the RenovoTAMP therapy platform via pressure-mediated

delivery technology to deliver gemcitabine, an FDA-approved chemotherapy, locally across the arterial wall to bathe tumor tissue in the

chemotherapy. RenovoGem is currently being evaluated in the Phase III TIGeR-PaC clinical trial study in Locally Advanced Pancreatic Cancer

(LAPC) patients. The Company plans to investigate RenovoGem in extrahepatic Cholangiocarcinoma (eCCA) in a clinical trial, which is anticipated

to begin in the first half of 2023.

is a clinical-stage biopharmaceutical company with a vision to disrupt the current paradigm of cancer treatment. Our mission is to lead

a revolution in oncology therapy by delivering its innovative and targeted intra-arterial (IA) delivery of chemotherapy directly to solid

tumors. The proprietary RenovoRx Trans-Arterial Micro-Perfusion (RenovoTAMP ) therapy platform aims to avoid the harsh

side effects typical of the current standard of care, or systemic delivery methods, thus improving patient well-being and, potentially

extension of life, so more time may be enjoyed with loved ones. RenovoTAMP utilizes approved chemotherapeutics with validated mechanisms

of action and well-established safety and clinical use, with the goal of improving their safety, tolerance, and widening their therapeutic

window by providing more targeted delivery at the location of the tumor tissue. RenovoRx's lead product candidate, RenovoGemTM,

is a combination of gemcitabine and its patented delivery system, RenovoCath , and is regulated by the FDA as a novel

oncology drug product to treat unresectable locally advanced pancreatic cancer (LAPC). RenovoGem is currently being studied in the Phase

III TIGeR-PaC clinical trial for the treatment of LAPC.

patent portfolio for its therapy platform and product candidates includes eight issued U.S. patents, one issued European patent, and

several additional patents pending in the US, EU and Asia. RenovoRx has been granted Orphan Drug Designation for intra-arterial delivery

of gemcitabine for the treatment of both pancreatic cancer and bile duct cancer (cholangiocarcinoma).

press release contains 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 our clinical trials and studies, including anticipated

timing, statements regarding the potential of RenovoTAMP , RenovoCath or RenovoGemTM or regarding

our ongoing TIGeR-PaC Phase III clinical trial study in LAPC, statements regarding the potential for our product candidates to treat

or provide clinically meaningful outcomes for certain medical conditions or diseases, and our preliminary financial results, cash position

and related ability to continue as a going concern. 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, clinical trials, therapy platform,

business plans, objectives and expected operating results, which are based on current expectations and assumptions that are subject to

known and unknown risks and uncertainties that may cause actual results to differ materially 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: the timing of the initiation, progress and potential results of our preclinical studies,

clinical trials and our research programs; the interim results may not be predictive of the outcome of our clinical trial, which may

not demonstrate sufficient safety and efficacy to support regulatory approval of our product candidate, or the regulatory authority may

disagree with our interpretation of the data; research and clinical development plans and timelines, and the regulatory process for our

product candidates; future potential regulatory milestones for our product candidates, including those related to current and planned

clinical studies; our ability to use and expand our therapy platform to build a pipeline of product candidates; our ability to advance

product candidates into, and successfully complete, clinical trials; the timing or likelihood of regulatory filings and approvals; 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; the commercialization potential of our product candidates, if approved; our ability and the potential to successfully manufacture

and supply our product candidates for clinical trials and for commercial use, if approved; future strategic arrangements and/or collaborations

and the potential benefits of such arrangements; our estimates regarding expenses, future revenue, capital requirements and needs for

additional financing and our ability to obtain additional capital; the sufficiency of our existing cash and cash equivalents to fund

our future operating expenses and capital expenditure requirements; our ability to retain the continued service of our key personnel

and to identify, hire and retain additional qualified personnel; the implementation of our strategic plans for our business and product

candidates; the scope of protection we are able to establish and maintain for intellectual property rights, including our therapy platform,

product candidates and research programs; our ability to contract with third-party suppliers and manufacturers and their ability to perform

adequately; the pricing, coverage and reimbursement of our product candidates, if approved; developments relating to our competitors

and our industry, including competing product candidates and therapies; negative impacts of the ongoing COVID-19 pandemic on our operations;

and other risks. 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.

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.

Statement of Operations Data

thousands, execpt for share and per share amount)

Strategic Communications

Pinto or Jack Perkins