Clinical trial · Interventional
Nicotinamide Chemoprevention for Keratinocyte Carcinoma in Solid Organ Transplant Recipients - Pivotal Trial
Nicotinamide Chemoprevention for Keratinocyte Carcinoma in Solid Organ Transplant Recipients: a Multicentre, Pragmatic Randomized Trial
- 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)
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.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Basal Cell | Basal Cell Carcinoma | ONTOLOGY_EXACT | 0.90 |
| Carcinoma, Squamous Cell | Squamous Cell Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Keratinocyte Carcinoma | — | UNRESOLVED | — |
| Non-melanoma Skin Cancer | Skin Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Nicotinamide | Drug | Niacinamide | ALIAS |
| Placebo | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Nicotinamide
- description
- Intervention Drug : Nicotinamide
- interventionNames
- Drug: Nicotinamide
- type
- PLACEBO_COMPARATOR
- label
- Placebo
- description
- Intervention: Placebo Oral Capsule
- interventionNames
- Drug: Placebo
Primary outcomes (1)
- measure
- Time to first biopsy-confirmed keratinocyte carcinoma (basal cell carcinoma or invasive cutaneous squamous cell carcinoma)
- timeFrame
- Up to 208 weeks
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥ 18 years old * Kidney, liver, heart, or lung transplant at least two years ago * History of at least one prior histologically-confirmed keratinocyte carcinoma or squamous cell carcinoma in situ * Currently immunosuppressed with a calcineurin inhibitor-based regimen (cyclosporine or tacrolimus) * Able to attend follow-up visits Exclusion Criteria: * Use of nicotinamide or niacin (≥250 mg daily) within past 12 weeks * Untreated localized skin cancer at baseline (patient can enrol after skin cancer treatment) * Biopsy-confirmed acute rejection episode within the past 12 weeks * Active liver disease (high AST \>3 times or bilirubin \>1.5 times) * Severe kidney disease (estimated glomerular filtration rate \<20 mL/min/1.73 m2) * Solid organ or hematologic malignancy, invasive melanoma, Merkel cell carcinoma, or metastatic skin cancer within the past five years * Pregnancy or lactation * Need for ongoing carbamazepine or primidone * Allergy to nicotinamide or any ingredient of the vitamin or placebo capsules
References
Publications (0)
Data not yet available