Phase 1 Melanoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People whose overall health and ability to carry out daily activities falls within a certain range, measured by a standard scale called ECOG, with a score of 0 (fully active) or 1 (restricted in strenuous activity but able to do light work).
- People who have been confirmed by laboratory tissue testing to have a type of cancer that cannot be removed by surgery — either Stage III or Stage IV melanoma (a type of skin cancer), or another solid tumour.
- People whose cancer has stopped responding to standard treatments (including targeted therapies), who are unable to tolerate standard treatments, or who have chosen not to pursue standard treatments.
- People whose cancer can be measured using standard imaging criteria (known as RECIST v1.1), meaning the tumour(s) are visible and trackable on scans.
- People whose tumour has one or more confirmed mutations in a gene called NRAS, which is known to drive cancer growth.
Who may not be able to join:
- People whose cancer has a known mutation in certain other genes (KRAS, HRAS, or BRAF), or known changes in other genes that drive cancer growth.
- People who have previously been treated with certain types of drugs that target the RAS-MAPK pathway — a signalling system involved in cancer cell growth — including drugs targeting ERK, MEK, RAF, or RAS.
- People with melanoma who have a blood test result showing a protein called LDH at more than twice the upper limit of the normal range.
- People who have cancer that has spread to the brain or spinal cord and is causing worsening neurological symptoms, or who need ongoing steroid medication to manage that spread.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 617-322-0731
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Part 1: Maximum Tolerated Dose (MTD) and/or RP2D of RLY-8161; Part 1: Number of participants with Adverse Events (AEs) or Serious Adverse Events (SAEs), with changes in vital signs, electrocardiograms (ECGs), and laboratory tests; Part 2: Objective Response Rate (ORR) of RLY-8161 as assessed by RECIST v1.1
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.