Non Melanoma Skin Cancer

7

Review clinical trials related to Non Melanoma Skin Cancer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Electrochemotherapy (ECT) in Patients With Primary Visceral Tumors and/or Secondary Visceral Localizations, of Any Histotype

This is an monocenter, single arm, clinical investigation that evaluate the impact of the method on the objective response rate (ORR) of visceral lesions undergoing electrochemotherapy. Electrochemotherapy is a well-defined method for the treatment of cutaneous and subcutaneous metastases of different tumor histotypes. Although still limited, the various experiences in the treatment of visceral localizations, particularly in liver metastases from colorectal cancer are promising and show that electrochemotherapy is a safe treatment, even in the case of lesions near large vessels or nerves. The investigators therefore propose a clinical investigation with a Medical Device according to EU Regulation 745/2017, using electrochemotherapy (Cliniporator) with bleomycin for the treatment of visceral, primary or secondary, unresectable localizations, with percutaneous or intraoperative technique (laparoscopic or laparotomy), as needed.

Participants needed: 24
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Istituto Oncologico Veneto IRCCSUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Male/Female ≥ 18 years [+3]

Absolute contraindications to invasive procedures [+7]

Status: Recruiting

EBNK-001 Allogeneic NK Cells With Low-Dose IL-15 ± Pembrolizumab in Advanced Solid Tumors

This Phase 1/2 study evaluates the safety, tolerability, and preliminary anti-tumor activity of EBNK-001 (allogeneic NK cells) given after lymphodepleting cyclophosphamide/fludarabine (CY/FLU) and supported with low-dose IL-15, administered either alone or in combination with pembrolizumab in adults with advanced/metastatic solid tumors. The study will determine a recommended Phase 2 dose (RP2D) and explore signals of clinical activity using RECIST-based response criteria.

Participants needed: 83
Trial details
Phase: Phase 1, Phase 2Biological sex: AllType: InterventionalSponsor: Essen BiotechUpdated: Feb 18, 2026Locations: 1
Eligibility criteria

Age ≥18 years. [+9]

Pregnant or breastfeeding. [+8]

Status: Recruiting

Skin Cancer and Hyperthermia and Radiotherapy

The SAHARA trial assesses wether combining ultrahypofractionated accelerated radiotherapy (RT) with hyperthermia is as effective as standard hypofractionated high-dose radiation in treating non-melanoma skin cancer (NMSC).

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Kantonsspital Winterthur KSWUpdated: Jun 15, 2025Locations: 4
Eligibility criteria

Personally signed and dated written informed consent [+7]

Other histology than BCC or SCC [+11]

Status: Recruiting

Effectiveness of Fractionated Laser Resurfacing to Protect Geriatric Skin From Actinic Neoplasia

This study is following up on previous studies that have demonstrated that geriatric subjects respond different to ultraviolet B (UVB) light than young subjects. The treatment of geriatric skin with dermal rejuvenation therapies (dermabrasion, fractionated laser resurfacing) restores the appropriate UVB response. Ongoing studies have tested the ability of fractionated laser resurfacing (FLR) to assess how long this wounding effect lasts-and have found that this appears to be a durable response which lasts for at least two years. The findings that FLR protects geriatric skin at two years is the impetus for this study. This study is an interventional study to assess if FLR treatment of one forearm of geriatric subjects with multiple actinic keratosis will result in the short-term removal of actinic keratosis, and the long-term decrease in levels of future actinic keratosis and other non-melanoma skin cancers in comparison to the untreated arm. Study length and visit: The first part of the study is completed in 1 day then there are follow up visits at 90 days and every 6 months for 5 years.

Participants needed: 72
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Wright State UniversityUpdated: Mar 25, 2025Locations: 1
Eligibility criteria

Diagnosed with Actinic Keratosis within the past 6 months [+5]

Uncontrolled Diabetes Mellitus [+8]

Status: Recruiting

Nicotinamide Chemoprevention for Keratinocyte Carcinoma in Solid Organ Transplant Recipients - Pivotal Trial

As patients live longer after receiving an organ transplant, there is a need to reduce the long-term side effects of the drugs used to prevent organ rejection. In particular, long-term use of these drugs increases the risk of skin cancer. Skin cancer is now a leading cause of illness and disfigurement after kidney, liver, heart, and lung transplantation. Given the increased risk and burden of skin cancer in transplant recipients, prevention is critical. Nicotinamide is a form of Vitamin B3 that has been shown to protect against skin cancer in the general population. However, it is unclear whether nicotinamide is effective among immune-suppressed transplant recipients. Investigators will conduct a clinical trial involving multiple transplant centres in Canada to evaluate whether oral nicotinamide (500 mg twice daily) is effective and safe for preventing skin cancer. Investigators will recruit 396 high-risk adult kidney, liver, heart, and lung transplant patients who have previously had at least one skin cancer. Patients will receive nicotinamide or sham tablets for up to 4 years. The results will inform efforts to improve the long-term health of transplant recipients.

Participants needed: 396
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Women's College HospitalUpdated: Feb 21, 2025Locations: 7
Eligibility criteria

Age ≥ 18 years old [+4]

Use of nicotinamide or niacin (≥250 mg daily) within past 12 weeks [+8]

Status: Not yet recruiting

Dermoscopy and Histopathology in Non-melanocytic Skin Tumors

The main aim of the study is to investigate the relation between dermoscopic findings in pre-operative diagnosis of non-melanocytic skin tumors and post-operative histopathology findings .

Participants needed: 20
Trial details
Biological sex: AllType: ObservationalSponsor: Assiut UniversityUpdated: Jul 26, 2024Duration: 10 Days
Eligibility criteria

All patients with NMST clinically of both genders in all ages with positive derm...

No exclusion criteria

Status: Recruiting

The Preventive Role of Fractionated Laser Resurfacing Against Actinic Neoplasia in an At-Risk Geriatric Population

The purpose of this study is to determine if the Fractionated Laser Resurfacing (FLR) procedure can protect one forearm/wrist from precancerous actinic keratosis (AKs) as well as prevent skin cancer in older subjects with active AKs. This study builds on a similar study ongoing at the Dayton Veterans Administration dermatology clinic. This study is also testing if a photograph of the skin can be used to predict where the AKs and an skin cancers will form.

Participants needed: 80
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Wright State UniversityUpdated: Jul 24, 2024Locations: 1
Eligibility criteria

Adult Males and Females aged 60 and older [+4]

More than 10 AKs on an extremity [+9]