Webster, TXNCT05157763Now EnrollingIRB Ready

Superficial Basal Cell Carcinoma Clinical Trial in Webster, TX

Access cutting-edge superficial basal cell carcinoma treatment through this clinical trial at a research site in Webster. Study-provided care at no cost to qualified participants.

Sponsored by MediWound Ltd

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See if you qualify for this Webster location

Preparing your pre-screening questions…

Expert Care in Webster

Access superficial basal cell carcinoma specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related superficial basal cell carcinoma treatment provided free

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Check if you qualify for this superficial basal cell carcinoma clinical trial in Webster, TX

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Webster

    Convenient for TX 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 Webster site if eligible
  4. 4Begin participation

About This Superficial Basal Cell Carcinoma Study in Webster

This study will be a multicenter, prospective, open label, one-arm study intended to assess the Safety and Efficacy of EscharEx (EX-02) in the treatment of Basal Cell Carcinoma. In patients with one primary superficial or nodular basal cell carcinoma lesion with a diameter of 5-10mm (Histologically confirmed BCC) located on the trunk or upper extremities (not including the hands), with well-defined borders and no previous radiation therapy.

Sponsor: MediWound Ltd

Who Can Participate

Inclusion Criteria

Male or female greater than age 18,
Patients with one primary superficial or nodular basal cell carcinoma lesion (Histologically confirmed BCC) located on the trunk or upper extremities (not including the hands), with well-defined borders and no previous radiation therapy.
Lesion is present for no longer than 4 years.
Lesion with a diameter of 5-10mm,
Patient and/or legally authorized representative (LAR) understands the nature of the procedure, is able and willing to adhere to the protocol regimen, and able to provide a written informed consent prior to any study procedure.

Exclusion Criteria

Evidence of Gorlin syndrome, neoplastic diseases (except actinic lesions), metastatic tumor or tumor with high probability of metastatic spread,
Other malignant cancers (non BCC) of the skin at the lesion's site,
Morphea-type basal cell carcinoma (MBCC) at the lesion's site (per biopsy report),
Any signs of infection at the lesion site including purulent discharge, tissue abscess, erysipelas, cellulitis, etc.,
Patients with any dermatological disease in the target lesion site or surrounding area (not including chronic actinic damage in the surrounding area),
History of allergy or atopic disease or a known sensitivity to pineapples, papaya, bromelain or papain, as well as known sensitivity to latex proteins (known as latex-fruit syndrome), bee venom or olive tree pollen,
Patients undergoing renal or peritoneal dialysis,
Any condition that would preclude safe participation in the study, e.g. evidence of significant or unstable cardiovascular, pulmonary, liver, hematological, immunological, or any immediate life threatening condition,
Concurrent acute injury or disease that might compromise the patient's welfare or the participation in the study,
Current (within last 12 months) severe alcohol or drug use disorder
Pregnant women (positive blood or urine pregnancy test) or nursing mothers,
Exposure to investigational intervention within 4 weeks prior to enrolment, or anticipated participation in another investigational drug trial or other intervention trial, while enrolled in the study.

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 Webster?

Yes, this clinical trial (NCT05157763) has an active research site in Webster, TX 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.

Superficial Basal Cell Carcinoma Treatment Options in Webster, TX

If you're searching for superficial basal cell carcinoma treatment options in Webster, TX, this clinical trial (NCT05157763) 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 Webster research site is actively enrolling participants for this clinical trial. You'll receive care from experienced superficial basal cell carcinoma 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 superficial basal cell carcinoma clinical trials near you to find additional studies recruiting in your area.

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