ClinConnect ClinConnect Logo
Search / Trial NCT03971643

Exploratory Study of IFX-1 in Patients With Pyoderma Gangrenosum

Launched by INFLARX GMBH · May 31, 2019

Trial Information

Current as of May 07, 2025

Completed

Keywords

ClinConnect Summary

Neutrophilic dermatoses are a spectrum of inflammatory disorders characterized by skin lesions resulting from a neutrophil-rich inflammatory infiltrate in the absence of infection. Pyoderma gangrenosum is associated with a neutrophilic leukocytosis, which is likely to be triggered by C5a. This study is set up based on the hypothesis that vilobelimab might be able to block C5a induced pro-inflammatory effects such as neutrophil activation and cytokine generation, potentially contributing to the local skin inflammation and tissue damage.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Diagnosis of an ulcerative form of pyoderma gangrenosum confirmed by the investigator
  • In addition, the subject must fulfill at least 3 of the following 6 criteria at screening:
  • History of
  • Pathergy (ulcer occurring at the sites of trauma)
  • Personal history of inflammatory bowel disease or inflammatory arthritis
  • History of papule, pustule or vesicle that rapidly ulcerated
  • Clinical examination (or photographic evidence) of
  • Peripheral erythema, undermining border, and tenderness at site of ulceration
  • Multiple ulcerations (at least 1 occurring on the lower leg)
  • Cribriform or "wrinkled paper" scar(s) at sites of healed ulcers
  • Subject has a minimum of 1 evaluable ulcer (≥2 cm2) on the lower extremity at screening
  • Exclusion Criteria:
  • Pyoderma gangrenosum target ulcer for more than 3 years before screening
  • Surgical wound debridement within the previous 2 weeks before screening
  • Use of intravenous antibacterials, antivirals, anti-fungals, or anti-parasitic agents within 30 days before screening
  • Any drug treatment for pyoderma gangrenosum including corticosteroids (\>10 mg), intralesional steroids, cyclosporine A, biologicals and immunosuppressives (with the exception of antibiotics for wound superinfection) used within a time of 5 half-lives of the drug before screening

About Inflarx Gmbh

Inflarx GmbH is a biopharmaceutical company focused on the development of innovative therapies for the treatment of autoimmune and inflammatory diseases. With a strong commitment to advancing medical science, Inflarx specializes in monoclonal antibody research, leveraging its proprietary technologies to create targeted treatments that address unmet medical needs. The company is dedicated to conducting rigorous clinical trials to evaluate the safety and efficacy of its drug candidates, aiming to improve patient outcomes and enhance quality of life. Through collaboration with leading research institutions and a team of experienced professionals, Inflarx is positioned at the forefront of therapeutic advancements in its field.

Locations

Sacramento, California, United States

Miami, Florida, United States

Tampa, Florida, United States

Saint Louis, Missouri, United States

Columbus, Ohio, United States

Hershey, Pennsylvania, United States

Pittsburgh, Pennsylvania, United States

Richmond Hill, Ontario, Canada

Rzeszów, , Poland

Wrocław, , Poland

Patients applied

0 patients applied

Trial Officials

Prof. Niels C. Riedemann, M.D., Ph.D.

Study Director

InflaRx GmbH

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials