Welcome to our dedicated page for Renovorx news (Ticker: RNXT), a resource for investors and traders seeking the latest updates and insights on Renovorx stock.
RenovoRx, Inc. reports news on targeted oncology drug delivery, the commercialization of RenovoCath®, and clinical development of its TAMP™ therapy platform. The company is a life-sciences issuer developing localized cancer therapies and commercializing RenovoCath, a patented FDA-cleared drug-delivery device used for temporary vessel occlusion and chemotherapeutic drug infusion.
Recurring updates cover RenovoCath adoption at U.S. cancer centers, intellectual-property protection for the device, financing activity, financial results, and presentations of clinical or pharmacologic data. News also tracks IAG, the investigational intra-arterial gemcitabine product candidate delivered via RenovoCath, including disclosures tied to the TIGeR-PaC trial in locally advanced pancreatic cancer and orphan drug designations for pancreatic and bile duct cancer.
RenovoRx (Nasdaq: RNXT) will host its fourth quarter and full year 2025 financial results and business highlights conference call on March 30, 2026 at 4:30 p.m. ET. Management will discuss RenovoCath adoption at U.S. cancer centers, clinical and commercial momentum, and pipeline updates.
The company said the Phase III TIGeR-PaC trial remains on track to complete enrollment in the first half of 2026 with final data expected in 2027. RenovoRx will also review plans for post-marketing registry studies and investigator-initiated trials; a replay will be available through April 13, 2026.
RenovoRx (Nasdaq: RNXT) announced a definitive private placement expected to raise approximately $10 million in gross proceeds through the sale of ~10.64 million common shares and ~5.32 million milestone warrants.
Proceeds aim to accelerate RenovoCath commercialization, reduce cash burn, and fund full enrollment of the pivotal Phase III TIGeR-PaC trial by mid-2026, with results targeted in 2027. Closing expected March 20, 2026, subject to customary conditions.
RenovoRx (Nasdaq: RNXT) reported accelerating commercial adoption of its FDA-cleared RenovoCath device, with 12 U.S. cancer centers now using the device and 33 centers requesting access — a threefold increase in the near-term sales pipeline since Q1 2025.
RenovoCath has been used in 700+ procedures since 2014, the Company expects at least 10 new patients to begin TAMP therapy in Q1 2026, and the board appointed Ramtin Agah, MD to Executive Chairman to support commercialization and clinical adoption.
RenovoRx (Nasdaq: RNXT) announced acceptance of a clinical data abstract for presentation at the 2026 Society of Interventional Radiology (SIR) Annual Scientific Meeting April 11–15, 2026 in Toronto. The abstract examines PET/CT metabolic response after transarterial microperfusion using the TAMP therapy platform in locally advanced pancreatic cancer.
Presentation is scheduled for April 13, 2026, 4:45–5:45 PM ET (Abstract No. 2229370) and was submitted by a multidisciplinary team including Dr. Mustafa Al-Roubaie of Moffitt Cancer Center.
RenovoRx (NASDAQ: RNXT) formed a dedicated RenovoCath Medical Advisory Board (MAB) to guide clinical and market strategy for its FDA-cleared RenovoCath device and TAMP therapy platform. The MAB unites leading U.S. interventional radiology experts to advise on investigator-initiated trials, real-world evidence, and commercialization within cleared indications.
The board will inform ongoing trials including a Phase III TIGeR-PaC study and a post-marketing registry, and support capital-efficient clinical study planning to broaden TAMP applications in hard-to-treat cancers.
RenovoRx (Nasdaq: RNXT) appointed Mark Voll as Chief Financial Officer, effective February 1, 2026. Voll brings 30+ years of financial leadership and experience scaling public companies through IPOs and exits.
He will support commercialization of RenovoCath, provide forward-facing stockholder communications, and help advance the Phase III TIGeR-PaC clinical trial. A transitional finance team will include Ronald B. Kocak and Lilly Huang.
RenovoRx (NASDAQ: RNXT) will present new clinical data on February 6, 2026 at the SIO Annual Scientific Meeting showing that the TAMP™ therapy platform can use a simplified external pressure transducer to obtain reliable intra-arterial pressure measurements during double-balloon RenovoCath procedures.
The study (Abstract 303) showed strong correlation to intravascular pressure wire measurements in a porcine model and found peak pressure is affected by controllable variables like balloon spacing and target vessel diameter, highlighting procedural optimization opportunities.
RenovoRx (Nasdaq: RNXT) announced acceptance of a clinical data abstract for presentation at the 2026 Society of Interventional Oncology Annual Scientific Meeting in Savannah, Feb 4–8, 2026.
The ePoster, presented Feb 6, 2026, examines real-time intravascular pressure measurements using the TAMP therapy platform and the FDA-cleared RenovoCath double-balloon catheter to optimize targeted chemotherapy delivery in solid tumors.
RenovoRx (Nasdaq: RNXT) announced expansion of commercial adoption of its FDA-cleared RenovoCath device from five active U.S. cancer centers in September 2025 to nine as of Jan 20, 2026, including City of Hope Cancer Center and Moffitt Cancer Center. The RenovoCath device enables the company’s TAMP™ localized chemotherapy delivery approach and is being integrated into oncology programs while related physician interviews and patient stories were publicized. RenovoRx reported approximately $900,000 in sales through September 2025 and says it built a dedicated commercial team by end of 2025 to accelerate adoption. Ongoing Phase III TIGeR-PaC trial sites are not counted among current commercial customers but could convert after full enrollment in H1 2026.
RenovoRx (Nasdaq: RNXT) announced that CEO Shaun Bagai will present at the AlphaNorth Capital Event on January 16-18, 2026 in Nassau, Bahamas. Mr. Bagai will provide updates on commercial adoption of RenovoCath (an FDA-cleared targeted drug-delivery device) and progress in the Phase III TIGeR-PaC trial evaluating intra-arterial gemcitabine for locally advanced pancreatic cancer (LAPC). He will also discuss a post-marketing observational registry collecting real-world safety and survival data across solid tumors and support for capital-efficient investigator-initiated trials in pancreatic cancer.
Investor one-on-one meetings can be requested via KCSA Strategic Communications.