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PRF Technologies Reports Expanded Preclinical Results for PRF-110 in Head-to-Head Comparison with Approved Benchmark

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PRF Technologies (Nasdaq: PRFX) reported expanded preclinical results for its lead candidate PRF-110 in a head-to-head study against approved benchmark ZYNRELEF in a validated porcine post-operative pain model.

Data showed comparable analgesic efficacy, slower absorption, enhanced local tissue retention and sustained exposure, supporting development as a single-administration, long-acting post-surgical analgesic aimed at reducing opioid use.

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AI-generated analysis. Not financial advice.

Positive

  • Preclinical porcine model showed analgesic efficacy comparable to ZYNRELEF
  • Slower systemic absorption suggests more gradual ropivacaine release at wound site
  • Enhanced local tissue retention and higher local Cmax indicate prolonged local availability
  • Both PRF-110 and comparator showed sustained systemic and local drug exposure
  • Single-administration, extended-release design targets reduced post-operative opioid use

Negative

  • Results are from preclinical porcine model, not human clinical trials
  • Company states further studies are needed to validate safety and efficacy in broader surgical settings

Market Reaction – PRFX

+14.89% $1.62 2.1x vol
15m delay 25 alerts
+14.89% Since News
+23.9% Peak in 10 min
$1.62 Last Price
$1.46 $2.28 Day Range
+$639K Valuation Impact
$4.93M Market Cap
2.1x Rel. Volume

Following this news, PRFX has gained 14.89%, reflecting a significant positive market reaction. Argus tracked a peak move of +23.9% during the session. Our momentum scanner has triggered 25 alerts so far, indicating elevated trading interest and price volatility. The stock is currently trading at $1.62. This price movement has added approximately $639K to the company's valuation. Trading volume is elevated at 2.1x the average, suggesting notable buying interest.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Gold for real-time data.

Peers on Argus

PRFX was moving while two sector peers in the momentum scan (BFRI, YCBD) also mo...
2 Up 1 Down

PRFX was moving while two sector peers in the momentum scan (BFRI, YCBD) also moved up around 4%, indicating a broader Healthcare/specialty pharma move rather than an entirely isolated reaction.

Historical Context

5 past events · Latest: May 28 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
May 28 AI platform update Positive +1.5% Advanced DeepSolar Predict AI platform toward commercial launch in renewables.
May 26 Preclinical pain data Positive -10.1% PRF-110 showed 72-hour analgesic activity comparable to approved ZYNRELEF in pigs.
Apr 28 IND clearance Positive -10.9% FDA cleared IND for OcuRing-K Phase II trial in cataract surgery patients.
Mar 27 Business update Positive -11.9% Year-end 2025 update with reduced net loss and cash position plus platform progress.
Mar 17 Commercial collaboration Positive -6.2% Commercial collaboration to scale DeepSolar AI platform across large solar portfolios.
Pattern Detected

PRFX has frequently traded down on prior positive operational and clinical updates over the last six months.

Regulatory & Risk Context

Short Interest: 10.29%
Short Interest
10.29% of float
0% 15% 30%+
moderate as of 2026-05-29 Days to cover: 1

Short positioning appears moderate, which can contribute to brisk moves in either direction if liquidity tightens or sentiment shifts sharply.

Market Pulse Summary

This announcement adds preclinical evidence that PRF-110 matches benchmark analgesic efficacy while ...
Analysis

This announcement adds preclinical evidence that PRF-110 matches benchmark analgesic efficacy while showing slower absorption and higher local Cmax. Investors may track translation into human trials and balance this promise against equity financing and short-interest risks.

Key Terms

pharmacokinetic, ropivacaine, cmax, extended-release
4 terms
pharmacokinetic medical
"The expanded results characterize the pharmacokinetic (PK) and tissue-distribution properties"
Pharmacokinetic describes how a drug moves through and leaves the body — how it is absorbed, spread to tissues, broken down and excreted — like tracking a package from pickup to delivery and disposal. For investors, these properties determine effective dose, safety risks, how often a medicine must be taken, and how reliably it works, which in turn influence clinical trial success, regulatory approval chances, production complexity and a drug’s commercial value.
ropivacaine medical
"extended-release formulation of ropivacaine designed to be deposited directly into the surgical"
Ropivacaine is a long‑acting local anesthetic used to numb specific parts of the body during surgery or for pain relief after procedures, delivered by injection near nerves or into the spine. For investors it matters because its use, patent status, manufacturing scale and regulatory approvals affect hospital drug spending and sales volumes much like a commonly used specialty tool; changes in competition, safety data or generic entry can materially alter a maker’s revenue stream.
cmax medical
"increased retention in local tissue along with higher local tissue exposure (Cmax), supporting"
Cmax is the highest concentration of a drug measured in the bloodstream after a dose, like the peak of a wave after a stone is dropped into water. It matters to investors because that peak helps regulators and doctors judge safety and likely effectiveness, informs dosing schedules, and is used to compare formulations or generics—data that can affect a drug’s approval, marketability, and commercial value.
extended-release medical
"an approved extended-release product used as a benchmark in the study"
Extended-release is a drug formulation designed to release its active ingredient slowly over an extended period so the medicine stays at steadier levels in the body and usually needs to be taken less often—think of a timed-release coffee versus sipping many short espressos. Investors care because extended-release versions can improve patient adherence, reduce side effects, and create product differentiation that supports higher pricing, longer commercial lifecycles, and clearer revenue visibility, while also attracting specific regulatory and manufacturing considerations.

AI-generated analysis. Not financial advice.

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Additional data reported by an independent research firm show comparable analgesic efficacy to ZYNRELEF alongside slower absorption and enhanced local tissue retention, reinforcing PRF-110’s potential as a long-acting, single-administration post-operative analgesic

TEL AVIV, Israel, June 25, 2026 (GLOBE NEWSWIRE) -- PRF Technologies Ltd. (Nasdaq: PRFX) (“PRF” or the “Company”), a clinical-stage specialty pharmaceutical company focused on reformulating established therapeutics for post-operative pain management, today announced expanded results from its previously reported preclinical study directly comparing its lead product candidate, PRF-110, to ZYNRELEF® (bupivacaine and meloxicam extended-release solution), an approved extended-release product used as a benchmark in the study. The expanded results characterize the pharmacokinetic (PK) and tissue-distribution properties of PRF-110 alongside the analgesic efficacy data previously announced.

PRF-110 is a proprietary, oil-based, viscous, clear extended-release formulation of ropivacaine designed to be deposited directly into the surgical wound bed prior to closure. The product candidate is being developed to provide prolonged local analgesia following surgery through a single administration at the surgical site, with the goal of reducing the use of opioids for post-surgical pain.

The study was conducted in a validated porcine post-operative pain model, using von Frey methodology, to assess both analgesic efficacy and PK properties of the two extended-release formulations.

Key Findings

  • Comparable analgesic efficacy: PRF-110 and ZYNRELEF demonstrated similar reductions in mechanical sensitivity, as measured by the von Frey test, indicating comparable pain-relief performance.
  • Favorable pharmacokinetic profile: PRF-110 exhibited a slower absorption rate relative to ZYNRELEF, suggesting a more gradual release of ropivacaine at the site of administration.
  • Enhanced tissue retention: PRF-110 showed increased retention in local tissue along with higher local tissue exposure (Cmax), supporting prolonged availability of the active compound at the target site.
  • Sustained exposure: Both formulations demonstrated sustained systemic and local drug levels, reinforcing their potential as long-acting analgesic solutions.

“These expanded findings reinforce our confidence in PRF-110 as a differentiated, long-acting solution for post-operative pain management,” said Efi Cohen-Arazi, Chief Executive Officer of PRF Technologies. “Its pharmacokinetic profile—characterized by slower absorption and enhanced local tissue retention—combined with analgesic efficacy comparable to an approved benchmark, potentially positions PRF-110 to address a significant unmet need in improving post-surgical recovery and patient comfort.”

“These results further strengthen the growing body of evidence supporting PRF-110,” Mr. Cohen-Arazi added. “We remain focused on advancing the program and unlocking its full clinical and commercial potential.”

PRF plans to continue advancing PRF-110 through additional studies to further validate its safety, efficacy and clinical utility across broader surgical settings.

ZYNRELEF is used in this release solely as a comparator product. ZYNRELEF is a registered trademark of Heron Therapeutics, Inc. PRF Technologies is not affiliated with Heron Therapeutics, Inc., and this announcement is not sponsored, endorsed or authorized by Heron Therapeutics, Inc.

About PRF-110

PRF-110 is a proprietary, oil-based, viscous, clear extended-release solution based on the local anesthetic ropivacaine and is being developed for the post-operative pain relief market. PRF-110 is designed to be deposited directly into the surgical wound bed prior to closure to provide localized and extended post-operative analgesia. The formulation is designed to remain in place at the surgical site, spread over and adhere to the wound surface, resist rapid clearance, and provide sustained local release of ropivacaine. PRF-110 is being developed to provide prolonged post-operative pain relief following a single administration, with the goal of reducing the need for repeated dosing and potentially reducing reliance on opioids after surgery.

About PRF Technologies

PRF Technologies (Nasdaq: PRFX) is a company focused on the reformulation of established therapeutics, and a developer of AI-driven energy optimization technologies through its DeepSolar platform. The Company’s pharmaceutical programs leverage a proprietary extended-release drug-delivery system intended to provide prolonged post-surgical pain relief while minimizing the need for repeated dosing and reducing reliance on opioids. Through DeepSolar, PRF also delivers advanced software solutions that enable both consumers and enterprises to monitor, forecast and optimize energy consumption — particularly in solar-integrated environments. This dual business model reflects PRF’s strategic commitment to applying precision technology across high-impact sectors including healthcare and sustainable energy. For more information, please visit www.prf-tech.com.

Notice Regarding Forward-Looking Statements

This press release contains forward-looking statements about PRF’s expectations, beliefs and intentions, including with respect to statements related to the prospects for PRF-110 and its development plan. Forward-looking statements can be identified by the use of forward-looking words such as “believe”, “expect”, “intend”, “plan”, “may”, “should”, “could”, “might”, “seek”, “target”, “will”, “project”, “forecast”, “continue” or “anticipate” or their negatives or variations of these words or other comparable words, or by the fact that these statements do not relate strictly to historical matters. These forward-looking statements are based on assumptions and assessments made in light of management’s experience and perception of historical trends, current conditions, expected future developments and other factors believed to be appropriate. Forward-looking statements in this press release are made as of the date of this press release, and the Company undertakes no duty to update or revise any such statements, whether as a result of new information, future events or otherwise. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties, many of which are outside of the Company’s control. Many factors could cause actual activities or results to differ materially from the activities and results anticipated in forward-looking statements, including, but not limited to, the following: the Company’s ability to continue as a going concern; its history of significant losses; its need to raise additional capital and its ability to obtain additional capital on acceptable terms, or at all; its dependence on the success of its initial product candidate, PRF-110, OcuRing-K, LayerBio Inc.’s lead product candidate, and the commercialization of the DeepSolar solution; the outcomes of preclinical studies, clinical trials and other research regarding PRF-110, OcuRing-K and future product candidates; its limited experience managing clinical trials; its ability to retain key personnel and recruit additional employees; its reliance on third parties for the conduct of clinical trials, product manufacturing and development; the impact of competition and new technologies; its ability to comply with regulatory requirements relating to the development and marketing of its product candidates; its ability to establish and maintain strategic partnerships and other corporate collaborations; the implementation of its business model and strategic plans for its business and product candidates; the scope of protection it is able to establish and maintain for intellectual property rights and its ability to operate its business without infringing the intellectual property rights of others; the overall global economic environment; its ability to develop an active trading market for its ordinary shares and whether the market price of its ordinary shares is volatile; its ability to maintain its listing on the Nasdaq Capital Market; and statements as to the impact of the political and security situation in Israel on its business. More detailed information about the risks and uncertainties affecting the Company is contained under the heading “Risk Factors” included in the Company’s most recent Annual Report on Form 20-F and in other filings that the Company has made and may make with the Securities and Exchange Commission in the future.

Contact:

Crescendo Communications, LLC
Tel: 212-671-1021
Email: prfx@crescendo-ir.com

Dr. Ehud Geller, Executive Chairman
PRF Technologies Ltd.
Tel: +972-54-4236711
Email: egeller@medicavp.com


FAQ

What did PRF Technologies (NASDAQ: PRFX) announce about PRF-110 on June 25, 2026?

PRF Technologies announced expanded preclinical results for its lead candidate PRF-110 in a head-to-head comparison with ZYNRELEF. According to PRF Technologies, the data detail pharmacokinetics, tissue distribution and analgesic efficacy in a validated porcine post-operative pain model using von Frey methodology.

How did PRF-110 compare to ZYNRELEF in the preclinical pain model for PRFX?

PRF-110 demonstrated comparable analgesic efficacy to ZYNRELEF in reducing mechanical sensitivity in a porcine pain model. According to PRF Technologies, both extended-release formulations showed similar von Frey test performance, indicating comparable pain-relief effects under the study conditions.

What pharmacokinetic advantages did PRF-110 show versus ZYNRELEF in PRFX’s study?

PRF-110 showed a slower absorption rate compared with ZYNRELEF, suggesting more gradual ropivacaine release. According to PRF Technologies, PRF-110 also exhibited enhanced local tissue retention and higher local tissue exposure (Cmax), supporting prolonged availability of the active drug at the surgical site.

What is PRF-110 and how is it intended to be used for post-operative pain?

PRF-110 is a proprietary, oil-based, viscous, clear extended-release formulation of ropivacaine. According to PRF Technologies, it is designed for single administration into the surgical wound bed before closure to provide prolonged local analgesia and potentially reduce opioid use after surgery.

What do the PRF-110 tissue retention results mean for PRFX investors?

The study showed increased local tissue retention and higher Cmax for PRF-110 compared with ZYNRELEF. According to PRF Technologies, this supports prolonged local drug availability, which may be important for developing a long-acting, single-dose post-operative analgesic, subject to future clinical validation.

What are the next development steps for PRF-110 after these preclinical PRFX results?

PRF Technologies plans to continue advancing PRF-110 through additional studies across broader surgical settings. According to PRF Technologies, future work aims to further validate the candidate’s safety, efficacy and clinical utility as a long-acting, single-administration post-operative pain management option.

Does PRF-110’s preclinical data suggest potential to reduce opioid use after surgery for PRFX?

PRF-110 is being developed with the goal of reducing post-surgical opioid use by providing prolonged local analgesia. According to PRF Technologies, its extended-release, single-administration design and sustained exposure profile support this development objective pending further clinical studies.