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NCT05442710RECRUITINGanonymous

Recovery From Acute Immune Failure in Septic Shock by Immune Cell Extracorporeal Therapy

Sponsor

Source record

Artcline GmbH

Phase

Source record

Phase 2

Modality

AI-normalized

protein therapy

Target

AI-normalized

Immune cell perfusion system aimed at enhancing immune competence in septic shock patients.

Indication / condition

AI-normalized

Sepsis, Severe

Intervention

Source record

ARTICE

Source & freshness

Source record

NCT ID

NCT05442710

Original source

ClinicalTrials.gov

Source last updated

May 25, 2025

Ingested at

Jun 16, 2026

Internal sync

Jun 16, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT05442710

Title

Recovery From Acute Immune Failure in Septic Shock by Immune Cell Extracorporeal Therapy

Sponsor

Artcline GmbH

Status

RECRUITING

Phase

Phase 2

Condition raw

Sepsis, Severe

Condition normalized

Sepsis, Severe

Modality raw

protein therapy

Modality normalized

protein therapy

Target raw

Immune cell perfusion system aimed at enhancing immune competence in septic shock patients.

Target normalized

Immune cell perfusion system aimed at enhancing immune competence in septic shock patients.

Interventions

ARTICE

Public preview

Source record

Artcline GmbH's clinical trial, 'Recovery From Acute Immune Failure in Septic Shock by Immune Cell Extracorporeal Therapy,' is currently recruiting participants to evaluate the efficacy of the ARTICE therapy in conjunction with standard care for severe sepsis patients. The trial's focus on enhancing immune function in septic shock patients addresses a significant unmet medical need, as current treatment options primarily focus on managing symptoms rather than improving immune response. The potential for ARTICE to reduce mortality and improve organ function could position it favorably in the critical care market, which is projected to grow significantly due to rising sepsis cases globally. Competitive analysis indicates that while several therapies target sepsis management, few focus on immune enhancement, providing a unique market niche for ARTICE. Diligence considerations should include the robustness of the trial design, the clarity of primary and secondary endpoints, and the regulatory pathway for potential commercialization.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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