Oradell, NJNCT07396376Now EnrollingIRB Ready

Diabetic Foot Ulcer Clinical Trial in Oradell, NJ

Access cutting-edge diabetic foot ulcer treatment through this clinical trial at a research site in Oradell. Study-provided care at no cost to qualified participants.

Sponsored by Eluciderm Inc

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Expert Care in Oradell

Access diabetic foot ulcer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related diabetic foot ulcer treatment provided free

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Check if you qualify for this diabetic foot ulcer clinical trial in Oradell, NJ

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Why Participate?

  • No-Cost Study Care

  • Local to Oradell

    Convenient for NJ residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Oradell site if eligible
  4. 4Begin participation

About This Diabetic Foot Ulcer Study in Oradell

ELU42 01 01 (SuperHealer42) is a Phase I/IIA open label study sponsored by Eluciderm, Inc. that evaluates the safety and preliminary effectiveness of ELU42, a topical small molecule designed to modulate Wnt signaling, for the treatment of chronic diabetic foot ulcers (DFU). ELU42 combines a tankyrase inhibitor (XAV939) with a novel derivatized hyaluronic acid excipient (DHA77) and is applied as a topical spray to the index ulcer. Fifteen adults with Wagner grade 1-2 diabetic foot ulcers that have been present for at least 4 weeks and up to 52 weeks will be enrolled across up to four U.S. clinical sites. After a 2 week run in period during which standard of care (SOC) is provided (off loading, dressings, and debridement), subjects will receive ELU42 applied on site by trained study staff or the investigator three times per week (Monday, Wednesday, Friday) for six weeks (up to 18 applications). Subjects will be followed weekly during treatment and for up to 6 weeks after the final dose; additional Healing Confirmation visits are scheduled if the wound closes to evaluate the subjects over a course of a 3 month period. The study's co-primary objectives are to assess safety (incidence and severity of adverse events and infections) and to measure percent area reduction (PAR) of the index ulcer at Weeks 4 and 6. Efficacy assessments will be performed by the site investigator using direct two axis planimetry and by automated evaluation using the Tissue Analytics platform (surface area, volume, and PAR). Secondary and exploratory assessments include patient reported outcomes (Wound Q and SF 36), frequency of complete wound healing, wound hydration metrics, and pharmacokinetic sampling in a subset of subjects. Contact information for potential participants and referring clinicians is available at each participating site.

Sponsor: Eluciderm Inc

Who Can Participate

Inclusion Criteria

Age 18 to ≤75 years;
Diagnosis of type 1 or type 2 diabetes mellitus;
A1C ≤ 10 (historical within 2 months accepted);
Index DFU Wagner grade 1-2 with post debridement area ≥1.0 cm2 and ≤8.0 cm2;
Index DFU present for 4-52 weeks;
Index ulcer ≥1 cm below malleoli;
Adequate perfusion per ABI/TcPO2/PVR/TBI or Doppler; plantar ulcers off loaded ≥14 days prior to treatment;
Ability to consent and attend visits;
Contraception requirements for females of childbearing potential.

Exclusion Criteria

Infected index ulcer or surrounding cellulitis;
Ischemic ulcers; osteomyelitis or exposed bone;
Recent systemic antibiotic requirement for active infection (eligibility after resolution and 7 day washout);
Acute/inactive Charcot preventing off loading; hemoglobin \< 10 g/dL (unless Sponsor approves);
ESRD requiring dialysis;
Recent/planned vascular procedure on target leg within 30 days;
Participation in other IP trials within 30 days;
Active alcohol/substance abuse within 3 months;
Pregnancy or lactation;
Other PI judged exclusions

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Oradell?

Yes, this clinical trial (NCT07396376) has an active research site in Oradell, NJ that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Diabetic Foot Ulcer Treatment Options in Oradell, NJ

If you're searching for diabetic foot ulcer treatment options in Oradell, NJ, this clinical trial (NCT07396376) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Oradell research site is actively enrolling participants for this clinical trial. You'll receive care from experienced diabetic foot ulcer specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all diabetic foot ulcer clinical trials near you to find additional studies recruiting in your area.

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