FDA regulatory failure or delay
Sigyn Therapy is a Class III device requiring PMA approval before market clearance.
- Scope
- Lead product candidate
- Materiality
- high
Sigyn Therapeutics, Inc. is a U.S.-based development-stage medical device company focused on extracorporeal blood purification technologies. Its pipeline includes Sigyn Therapy for infectious disease disorders, along with ChemoPrep and ChemoPure for oncology applications, all designed to operate through hospital dialysis and CRRT infrastructure.
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| % | |
|---|---|
| Sigyn Therapy | 0% Single-use extracorporeal blood purification device designed to remove pathogens, toxins, and cytokines. |
| ChemoPrep | 0% Cancer-treatment adjunct intended to reduce circulating exosomes before chemotherapy administration. |
| ChemoPure | 0% Post-chemotherapy blood purification concept designed to remove off-target chemotherapy from blood. |
| Research and development | 100% Pre-clinical studies, device design, and regulatory advancement for future commercialization. |
The company is developing products for hospitals, dialysis providers, and clinical centers that treat severe infectious...
Would use Sigyn Therapy for severe infectious disease and inflammatory conditions if cleared.
Would deploy the device on existing renal replacement machines for blood purification use cases.
Potential users of ChemoPrep and ChemoPure to improve chemotherapy delivery and reduce toxicity.
Support pre-clinical validation and first-in-human studies for the company’s device pipeline.
Would help commercialize cleared products through established healthcare channels.
Sigyn Therapeutics is headquartered in San Diego, California and is organized as a Delaware corporation...
The company’s strategy is to advance Sigyn Therapy through pre-clinical and clinical development toward FDA clearance,...
FDA clearance is required before commercialization of the lead device.
ChemoPrep and ChemoPure need evidence to support future adoption in cancer care.
Commercialization depends on cGMP-compliant production and reliable suppliers.
Established distribution channels could accelerate market access after clearance.
Sigyn is exposed to the risks typical of early-stage medical device developers: regulatory uncertainty, clinical trial...
Sigyn Therapy is a Class III device requiring PMA approval before market clearance.
The company states it needs additional capital and has no assurance financing will be available.
Pre-clinical and first-in-human results may not support efficacy or safety claims.
Manufacturing relies on third-party vendors and contract manufacturers for components and cGMP output.
Even if cleared, hospitals and dialysis providers must adopt a new extracorporeal therapy.
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: 29.4.2026