Advocating for Patients: Letter to the FDA on RP1 Treatment Access

Hundreds of patients, families, and friends have shared their stories with AIM at Melanoma about the urgent need for access to RP1+nivolumab. We are grateful to everyone who contributed. Yesterday, along with several other melanoma organizations, we sent a letter to the FDA urging them to make RP1 available while remaining regulatory issues are addressed.
The full letter is embedded below for your reference. Click on the image to enlarge it, or download the PDF using the link beneath the letter.
Recent Posts

Best-in-Class Real-World Data Support Early Amtagvi® Treatment in Advanced Melanoma

Moderna, Merck’s Skin Cancer Vaccine Shows Sustained Benefit in Five-Year Follow-Up

Reflecting on Melanoma Treatment in 2025 and Looking to the Future in 2026

The Integrative Care Approach



