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Painreform Ltd - PRFX STOCK NEWS

Welcome to our dedicated page for Painreform news (Ticker: PRFX), a resource for investors and traders seeking the latest updates and insights on Painreform stock.

Company Overview

PainReform Ltd is a clinical-stage specialty pharmaceutical company dedicated to the reformulation of established pain therapeutics. With a focus on innovation within the postoperative analgesia and extended-release drug-delivery space, the company is committed to transforming pain management for both physicians and patients. By leveraging the FDA 505(b)(2) regulatory pathway, PainReform aims to enhance the clinical efficacy of existing medications while reducing adverse effects and optimizing dosing convenience.

Core Technologies and Therapeutic Advances

PainReform’s portfolio is anchored by its lead product candidate, PRF-110, which is based on the local anesthetic ropivacaine. Utilizing a proprietary, oil-based, viscous solution, PRF-110 is deposited directly into the surgical wound bed prior to closure. This innovative approach ensures localized, extended postoperative analgesia by maintaining therapeutic drug concentrations at the site of tissue injury over an extended period. The formulation addresses common limitations of traditional pain management therapies by reducing the necessity for repeated dosing and potentially lowering reliance on opioids.

Operational Strategy and Market Position

The company operates within the niche of drug reformulation, addressing specific clinical needs within the pain management segment. Through its disciplined focus on reformulating proven therapeutics, PainReform differentiates itself by applying unique technologies that enhance drug performance and patient compliance. The company’s operational model blends ongoing clinical research with strategic process improvements designed to bolster future commercialization efforts, thereby ensuring a resilient market presence in a dynamic therapeutic landscape.

Competitive Landscape and Differentiating Factors

PainReform competes in a complex landscape where innovation in drug delivery systems is critical to success. Unlike companies that develop entirely new molecular entities, PainReform capitalizes on reformulating established therapies to improve their safety and efficacy profiles. This approach allows the company to navigate regulatory pathways more efficiently while providing significant clinical benefits. Its extended-release technology is a key differentiator, offering both a therapeutic and operational advantage in a competitive market characterized by high standards of care and rigorous regulatory oversight.

Product Focus and Clinical Advantages

At the heart of PainReform’s clinical efforts is PRF-110, a product designed to address the unmet need for sustained postoperative pain relief. The product's oil-based, clear solution enables a streamlined mode of application and controlled drug release, tailoring pain management to the procedural landscape. By depositing the medication directly into the surgical wound bed, the company’s strategy minimizes the potential for systemic side effects and improves the overall patient experience. This method supports a growing clinical consensus that targeted, extended-release formulations can substantially improve postoperative recovery trajectories.

Industry Insights and Technological Integration

Within the specialty pharmaceutical sector, the intersection of drug reformulation and advanced delivery platforms represents a significant area of innovation. PainReform’s approach reflects a broader industry trend that prioritizes patient-centric therapies designed to deliver tangible clinical improvements. The integration of advanced drug-delivery systems not only refines the pharmacokinetic profile of established agents but also reinforces the company’s commitment to clinical excellence and operational efficiency. By adhering to rigorous regulatory standards and leveraging industry expertise, PainReform continues to evolve its technology platform, setting benchmarks in extended-release formulations and targeted therapeutic interventions.

Commitment to Quality and Clinical Validation

PainReform’s development strategy is reinforced by a commitment to clinical validation and quality assurance. Robust compatibility studies and ongoing clinical trials underscore the safety and efficacy of its formulations, positioning the company as a trusted entity within the pharmaceutical research community. Each phase of development is guided by stringent quality controls and backed by scientific data, ensuring that the therapeutic benefits of its products are communicated clearly to healthcare professionals and regulatory bodies alike.

Summary

In summary, PainReform Ltd stands as a specialist in the reformulation of pain therapeutics, harnessing innovative extended-release drug-delivery systems to address postoperative pain. Its focused approach, centered around PRF-110 and similar candidates, positions the company favorably within a competitive and evolving market. With an emphasis on clinical benefits, operational efficiency, and regulatory compliance, PainReform continues to advance a portfolio that is both strategic and clinically transformative, ensuring that it meets the essential needs of modern pain management.

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PainReform (Nasdaq: PRFX) has announced the pricing of a $4 million public offering, consisting of 5,000,000 ordinary shares and warrants. The offering is priced at $0.80 per share with accompanying warrants to purchase additional shares.
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PainReform (Nasdaq: PRFX) announces groundbreaking results from studies showing superior in-vitro release rates of PRF-110 for post-surgical pain management. PRF-110 released 34%-77% more drug over 96 hours compared to industry leaders, promising extended pain relief and reduced opiate dependency.
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PainReform (Nasdaq: PRFX) achieves 50% enrollment in Phase 3 clinical trial for PRF-110 in bunionectomy. No serious adverse events reported. Top-line data expected by mid-2024.
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PainReform Ltd. (PRFX) provides a business update, reporting enrollment progress in Phase 3 clinical trial for PRF-110, a post-operative pain relief drug. The company aims to announce top-line data by mid-2024. Financially, research and development expenses increased, while general and administrative expenses decreased. The net loss for 2023 was $9.3 million, with cash and cash equivalents of $8.0 million.
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PainReform Ltd. (Nasdaq: PRFX) announced its participation at The Microcap Conference on January 30 - February 1, 2024, where CEO Ilan Hadar will present on Track 2 and Track 5. The company will also hold one-on-one meetings with investors and provided contact information for meeting requests and conference registration.
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PainReform Ltd. (Nasdaq: PRFX) reported in vitro test results comparing its lead product, PRF-110, with the industry leader as a topical analgesia for postoperative pain relief. PRF-110 demonstrated superior formulation properties with respect to surface-tissue spreading, including a greater ability to spread evenly due to its viscosity (PRF-110 1,500 cP vs. industry leader 3,000 cP).
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PainReform Ltd. (Nasdaq: PRFX) announces a definitive agreement for the immediate exercise of outstanding warrants to purchase up to 467,896 ordinary shares at a reduced exercise price of $2.85 per share, registered pursuant to an effective registration statement on Form F-1 (File No. 333-274220).
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PainReform Ltd. (Nasdaq: PRFX) reports enrollment of first patients for the second part of Phase 3 clinical trial in bunionectomy. The company provided a business update for the third quarter ended September 30, 2023, highlighting the progress of their lead drug candidate, PRF-110, targeting the post-operative extended pain relief market. The update includes details about the initiation of the second part of the Phase 3 trial in bunionectomy, with the enrollment of the first patients and plans for continued enrollment of up to 400 patients in the double-blind study at multiple clinical sites in the U.S. The update also covers the financial results for the nine months ended September 30, 2023, including research and development expenses, general and administrative expenses, financial income, net, and net loss.
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PainReform plans to commence second part of Phase 3 trial for PRF-110 in Q4 2023, with results expected in mid-2024. Positive safety data from first part of trial suggests potential advantage over opioids. PRF-110 has key surgical benefits and addresses unmet need in postoperative pain market.
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PainReform announces positive safety and PK data of PRF-110 from Phase 3 clinical trial
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FAQ

What is the current stock price of Painreform (PRFX)?

The current stock price of Painreform (PRFX) is $2.09 as of April 4, 2025.

What is the market cap of Painreform (PRFX)?

The market cap of Painreform (PRFX) is approximately 1.8M.

What is the primary focus of PainReform Ltd?

PainReform Ltd is focused on reformulating established pain therapeutics to improve efficacy, safety, and patient convenience. Its lead candidate, PRF-110, exemplifies its commitment to enhanced postoperative pain management.

How does PainReform differentiate its product offerings?

The company differentiates its product portfolio by utilizing a proprietary extended-release drug-delivery system that allows for prolonged localized analgesia. This reduces the need for repeated dosing and potentially lowers opioid requirements.

What regulatory pathway does PainReform utilize for its products?

PainReform leverages the US FDA 505(b)(2) regulatory pathway, which supports the reformulation of established therapeutics by relying on existing data to expedite development.

How does PRF-110 work in managing postoperative pain?

PRF-110 is a viscous, oil-based formulation based on ropivacaine. It is applied directly to the surgical wound bed, providing localized and sustained analgesic effects, thereby enhancing pain relief during the postoperative period.

What are the clinical advantages of PainReform's extended-release formulations?

The extended-release formulations offer sustained therapeutic drug levels at the site of administration, reducing the need for frequent dosing and lowering the risk of systemic side effects. This approach promotes better overall pain management and recovery.

How does PainReform maintain its competitive edge in the specialty pharmaceutical market?

By focusing on reformulation rather than entirely new molecular entities, PainReform benefits from established safety profiles while enhancing clinical performance. Its unique drug delivery innovations and adherence to rigorous regulatory standards further reinforce its competitive position.

What market segment does PainReform primarily serve?

PainReform primarily serves the postoperative pain management segment, addressing a significant need in surgical recovery through its localized and extended-release pain relief solutions.

How does PainReform ensure the quality and efficacy of its products?

Quality and efficacy are ensured through robust clinical research, stringent compatibility studies, and adherence to high regulatory standards. The company’s development process is characterized by ongoing clinical validation and scientific rigor.
Painreform Ltd

Nasdaq:PRFX

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1.85M
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0.79%
4.58%
7.21%
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