Welcome to our dedicated page for Sigyn Therapeutics news (Ticker: SIGY), a resource for investors and traders seeking the latest updates and insights on Sigyn Therapeutics stock.
Sigyn Therapeutics, Inc. (OTCQB: SIGY) is a San Diego-based innovator developing blood purification technologies to combat life-threatening inflammatory conditions. This page serves as the definitive source for tracking SIGY's progress in advancing Sigyn Therapy™ and its complementary platforms targeting chemotherapy optimization and immunotherapy enhancement.
Investors and medical professionals will find timely updates on clinical milestones, regulatory developments, and strategic initiatives. Key focus areas include first-in-human studies for endotoxemia treatment, advancements in ImmunePrep™ antibody optimization, and progress toward Nasdaq listing requirements through recent corporate restructuring.
Our curated news stream covers essential updates including trial protocol finalizations, technology validation results, partnership announcements, and financial disclosures. All content is vetted for accuracy and relevance to SIGY's mission of addressing unmet needs in sepsis management, cancer care, and infectious disease treatment.
Bookmark this page for streamlined access to SIGY's evolving story in medical technology. Check regularly for developments that could influence both patient outcomes and long-term corporate valuation in this emerging therapeutic sector.
Sigyn Therapeutics (OTCQB: SIGY) will present at LD Micro Main Event XIX on Tuesday, October 21, 2025 at 4:00 PM PT at the Hotel del Coronado in San Diego.
Jim Joyce, CEO and inventor, will deliver the company presentation. The three-day conference runs October 19–21, 2025, features about 120 companies presenting in half-hour slots, and includes one-on-one investor meetings and a closing reception.
Investors can attend in person or register to watch the virtual presentation.
Sigyn Therapeutics (OTCQB: SIGY) will present at LD Micro Main Event XIX on Tuesday, October 21, 2025 at 4:00 PM PT at the Hotel del Coronado in San Diego. CEO and inventor Jim Joyce will deliver the presentation and the company will be available for investor meetings during the three-day event running October 19–21, 2025.
The conference features ~120 companies presenting in half-hour slots and includes keynotes, company presentations, one-on-one investor meetings, and a closing reception. A virtual registration option is available for the presentation.
Sigyn Therapeutics (OTCQB:SIGY) has been featured in a new research report by Goldman Small Cap Research, highlighting the company's development of next-generation blood purification therapies. The company's flagship product, Sigyn Therapy™, is a first-in-class device targeting severe inflammatory disorders, primarily sepsis and end stage renal disease (ESRD).
The device has demonstrated capability to reduce bacterial toxins, inflammatory cytokines, hepatic toxins, and infectious viral pathogens from human blood plasma. Additionally, Sigyn is developing medical devices to enhance cancer drug treatment effectiveness.
According to the research report, Sigyn plans to submit multiple Breakthrough Device submissions this year and expects to commence an ESRD feasibility study within the next 12 months. The study could yield data within 6 months of completion. Goldman Small Cap Research has issued a price target for SIGY, suggesting the company is currently undervalued compared to peers.
Sigyn Therapeutics (OTCQB:SIGY), a developer of next-generation blood purification therapies, is the subject of a new research report by Goldman Small Cap Research. The company's flagship product, Sigyn Therapy™, is a first-in-class device targeting severe inflammatory disorders, primarily sepsis and end-stage renal disease (ESRD).
The device has demonstrated effectiveness in reducing bacterial toxins, inflammatory cytokines, hepatic toxins, and infectious viral pathogens from human blood plasma. Additionally, Sigyn is developing medical devices to enhance cancer drug treatment effectiveness.
According to the research report, Sigyn plans to submit multiple Breakthrough Device submissions this year and expects to commence an ESRD feasibility study within the next 12 months. Data from this trial could be available within 6 months of study completion.
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