Recruiting
Phase 3

Nicotinamide

Sponsor:

Women's College Hospital

Code:

NCT05955924

Conditions

Non-melanoma Skin Cancer

Carcinoma, Squamous Cell

Carcinoma, Basal Cell

Keratinocyte Carcinoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Nicotinamide

Placebo

Study Details

Brief summary:

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

Non-melanoma Skin Cancer

Carcinoma, Squamous Cell

Carcinoma, Basal Cell

Keratinocyte Carcinoma

Study ID

NCT05955924

Start date

Aug 28, 2023

Status verified date

Feb, 2025

Completion date

Aug, 2027

Anticipated

Primary completion date

Aug, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

396 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

experimental: Nicotinamide

Intervention Drug : Nicotinamide

placebo comparator: Placebo

Intervention: Placebo Oral Capsule

Interventions

Nicotinamide

Oral nicotinamide (500 mg) twice daily

Placebo

Matching placebo capsule twice daily

Primary outcome measure

  • Time to first biopsy-confirmed keratinocyte carcinoma (basal cell carcinoma or invasive cutaneous squamous cell carcinoma) [ Time Frame: Up to 208 weeks ]

Central Contacts and Locations

Central contacts

Stephanie Jewell, BSc. Hons

416 351-3732sprintr@wchospital.ca

Locations

University of Alberta

Recruiting

Edmonton, Alberta, Canada, T6G 2R3

Contacts

Principal Investigator:

Sita Gourishankar

Vancouver General Hospital

Recruiting

Vancouver, British Columbia, Canada, V5Z 1M9

Contacts

Principal Investigator:

Sunil Kalia

St. Paul's Hospital

Recruiting

Vancouver, British Columbia, Canada, V6Z 1Y6

Contacts

Principal Investigator:

John Gill

The Ottawa Hospital

Recruiting

Ottawa, Ontario, Canada, K1Y 4E9

Contacts

Christine Lennox

clennox@ohri.ca

Principal Investigator:

Jennifer Beecker

Toronto General Hospital

Recruiting

Toronto, Ontario, Canada, M5G 2C4

Contacts

Principal Investigator:

An-Wen Chan

Women's College Hospital

Recruiting

Toronto, Ontario, Canada, M5S 1B2

Contacts

Stephanie Jewell

SPRINTR@wchospital.ca

Principal Investigator:

An-Wen Chan

More Information

Sponsor

Women's College Hospital

Last update posted

Feb 21, 2025

Last verified

Feb, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-28. This information was provided to ClinicalTrials.gov by Women's College Hospital on 2025-02-21. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.