RecruitingPhase 2Phase 3NCT06624644

A Trial of LNS8801 With or Without Pembrolizumab in Patients With Refractory Melanoma

A Multicenter, Open-Label, Randomized, Controlled Study to Assess the Antitumor Activity of LNS8801 With and Without Pembrolizumab in Patients With Treatment-Refractory, Unresectable Melanoma


Sponsor

Linnaeus Therapeutics, Inc.

Enrollment

135 participants

Start Date

Aug 6, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to understand if a new drug called LNS8801 can safely treat patients with melanoma. The primary question to be answered is what is the average length of time during which melanoma does not grow or spread after starting treatment with LNS8801? Researchers will compare LNS8801 taken alone or LNS8801 taken together with another drug called pembrolizumab to other therapies as decided by the treating doctor. 135 patients will be randomly (like flipping a coin) placed in 3 treatment groups. In the first group (LNS8801 only) - Patients will take 125mg tablet of LNS8801 by mouth once per day every day for up to 2 years. In the second group (LNS8801 + pembrolizumab) - Patients will take 125mg tablet of LNS8801 by mouth once per day plus 200 mg of pembrolizumab by IV infusion once every 3 weeks for up to 2 years. In the third group, called Physician's Choice (PC), patients will receive chemotherapy (dacarbazine or temozolomide) or immunotherapy (pembrolizumab, nivolumab/relatlimab or nivolumab/ipilimumab) as determined by their treating physician. How often the patient visits the clinic visits will depend on the treatment group. Besides returning to the clinic for treatment, the patient will undergo periodic safety assessments and other required study procedures such as imaging assessments.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests LNS8801 — an oral drug that activates a protein receptor on immune cells — with or without the immunotherapy drug pembrolizumab in people with metastatic melanoma (skin cancer that has spread) that no longer responds to standard immunotherapy. The goal is to see if this combination can overcome resistance to prior treatment. **You may be eligible if...** - You have unresectable and/or metastatic cutaneous melanoma - Your cancer stopped responding to anti-PD-1 immunotherapy (like pembrolizumab or nivolumab) - You also received anti-CTLA-4 therapy and/or BRAF-targeted therapy, or were found ineligible for those - Your tumor has 2 copies of the functional GPER gene - You have measurable disease and good physical health (ECOG 0–1) - You are able to swallow tablets **You may NOT be eligible if...** - Your cancer still responds to standard immunotherapy - You have not tried anti-PD-1 therapy - You have a rare melanoma subtype (such as blue nevus melanoma) - You have serious heart, liver, or autoimmune conditions Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BIOLOGICALLNS8801

G protein-coupled estrogen receptor (GPER) agonist

BIOLOGICALPembrolizumab

Recombinant monoclonal antibody (anti-PD1)

DRUGChemotherapy (dacarbazine or temozolomide)

chemotherapy (dacarbazine, temozolomide)

BIOLOGICALImmunotherapy (Pembrolizumab)

pembrolizumab

BIOLOGICALImmunotherapy (nivolumab and relatlimab)

nivolumab and relatlimab

BIOLOGICALImmunotherapy (ipilimumab and nivolumab)

ipilimumab and nivolumab


Locations(9)

USC Newport Beach

Newport Beach, California, United States

UCSF

San Francisco, California, United States

Stanford

Stanford, California, United States

University of Colorado Anschutz

Aurora, Colorado, United States

University of Colorado

Denver, Colorado, United States

Moffitt Cancer Center

Tampa, Florida, United States

Dana Farber

Boston, Massachusetts, United States

University of New Mexico

Albuquerque, New Mexico, United States

UPenn

Philadelphia, Pennsylvania, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06624644


Related Trials