Clinical trial · Interventional
Rhenium-Skin Cancer Therapy (SCT) for the Treatment of Non-Melanoma Skin Cancer.
Efficacy of Personalised Irradiation With Rhenium-Skin Cancer Therapy (SCT) for the Treatment of Non-Melanoma Skin Cancer: A Phase IV, Multi-Centre, International, Open-Label, Single Arm Study.
NCT05135052CI-TRIAL-00089687EPIC-Skinactive not recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Efficacy of Personalised Irradiation with Rhenium-Skin Cancer Therapy (SCT) for the treatment of non-melanoma skin cancer; a phase IV multi-centre, international, open label, single arm study.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-melanoma Skin Cancer | Skin Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Rhenium-SCT | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment arm
- description
- Treatment with Rhenium-SCT, Single treatment.
- interventionNames
- Device: Rhenium-SCT
Primary outcomes (1)
- measure
- Complete Response (CR) with Modified Visual RECIST tool
- timeFrame
- 12 months
- description
- To assess the proportion of lesions achieving complete response (CR) as per MODIFIED VISUAL RECIST criteria
Secondary outcomes (3)
- measure
- SKINDEX-16 QoL Questionnaire
- timeFrame
- 6 months and 12 months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Stage I or II BCC or SCC (SCC Well to Moderately Differentiated), and clinically node negative disease 2. Confirmed Histology, and with depth of lesion noted 3. Subjects with up to 3 lesions suitable to enter the study (subjects with more than 3 lesions are not excluded from the study, however 3 target lesions are determined for study evaluation only.) 4. Subjects able and willing to comply with the requirements of the study 5. Age \>=18 years 6. Informed Consent signed by the subject consenting to undergo the study 7. Lesions up to 8cm2 8. Lesions with a depth up to 3mm confirmed on biopsy report AND deemed appropriate clinically by treating clinician 9. Subjects who are not deemed suitable for surgery, for example due to tumour location, performance status or other comorbidities as deemed relevant by the treating clinician 10. Patients who may have declined Surgery and/or fractionated Radiation Therapy Exclusion Criteria: 1. Inability to personally provide written informed consent or to understand and collaborate throughout the study 2. Inability or unwillingness to comply with study requirements 3. Prior treatment with surgery or radiation therapy for their target lesion(s) 4. Depth of lesion greater than 3mm as defined by Biopsy and/or clinical assessment 5. Lupus and Scleroderma 6. Basal cell naevus syndrome, xeroderma, vitiligo and albinism 7. Prior laser at the tumour site 8. Malignant melanoma systemic therapy ongoing 9. Any ongoing treatment for malignancy, or in the last 4 weeks prior to study entry 10. A tumour affecting nerves or bony structures 11. Clinical concern of metastatic disease 12. Pregnancy and/or Lactation 13. Pathological exclusions: Perineural Invasion, Lymphovascular invasion 14. Anatomical exclusions: NMSC's of the Medial canthus, eyelid margin (upper and lower), Vermillion lip
References
Publications (0)
Data not yet available
No reference posted for this study.