Recruiting
Phase 2
Phase 3

LNS8801

Sponsor:

Linnaeus Therapeutics, Inc.

Code:

NCT06624644

Conditions

Melanoma (Skin Cancer)

Melanoma Stage IIIB-IV

Cutaneous Melanoma

Unresectable Melanoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

LNS8801

Pembrolizumab

Chemotherapy (dacarbazine or temozolomide)

Immunotherapy (Pembrolizumab)

Immunotherapy (nivolumab and relatlimab)

Study Details

Brief 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.

Conditions

Melanoma (Skin Cancer)

Melanoma Stage IIIB-IV

Cutaneous Melanoma

Unresectable Melanoma

Study ID

NCT06624644

Start date

Aug 6, 2025

Status verified date

Sep, 2025

Completion date

Feb, 2031

Anticipated

Primary completion date

Feb, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Confirmed unresectable and/or metastatic cutaneous melanoma.
  • 2 copies of the fully functional form of GPER protein-coding sequence.
  • Eligible for and willing to receive 1 or more of the physician's choice (PC) therapies.
  • Able to swallow tablets.
  • Progressed on treatment with an anti-PD-1 monoclonal antibody (mAb) administered either as monotherapy or in combination with other therapies.
  • Received an anti-CTLA-4 and/or BRAF containing regimen or is not eligible for or has declined anti-CTLA-4 and/or BRAF therapy prior to and for this study.
  • Measurable disease.
  • Eastern Cooperative Oncology Group Performance Status of 0 to 1.

Exclusion Criteria:

  • Blue nevus subtype, mucosal, acral lentiginous, or uveal/ocular/choroidal Melanoma.
  • Previous anti-cancer or investigational drug/device treatment within 4 weeks of the first dose of study drug.
  • Radiotherapy within 2 weeks of starting study drug.
  • Allogeneic tissue/solid organ transplant.
  • Unstable autoimmune or immunodeficiency disease.
  • Other concurrent health issues that would make participation or completion of the study difficult.
  • Prior reaction to anti PD-1 therapy that would make treatment with pembrolizumab unadvisable.
  • Other protocol-defined inclusion/exclusion criteria may apply.

Study Design

Enrollment

135 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: LNS8801 Monotherapy

125 mg LNS8801 by mouth every day

experimental: LNS8801 + Pembrolizumab

125 mg LNS8801 by mouth every day plus 200 mg Pembrolizumab by IV infusion once every 3 weeks.

active comparator: Physician's Choice

patients may receive chemotherapy or immunotherapy as determined by physician.

Interventions

LNS8801

G protein-coupled estrogen receptor (GPER) agonist

Pembrolizumab

Recombinant monoclonal antibody (anti-PD1)

Chemotherapy (dacarbazine or temozolomide)

chemotherapy (dacarbazine, temozolomide)

Immunotherapy (Pembrolizumab)

pembrolizumab

Immunotherapy (nivolumab and relatlimab)

nivolumab and relatlimab

Immunotherapy (ipilimumab and nivolumab)

ipilimumab and nivolumab

Primary outcome measure

  • Compare progression-free survival (PFS) of LNS8801 + pembrolizumab vs PC arms as assessed by RECIST v1.1. [ Time Frame: up to 2 years. ]

Central Contacts and Locations

Central contacts

Locations

USC Newport Beach

Recruiting

Newport Beach, California, United States, 92663

Contacts

UCSF

Recruiting

San Francisco, California, United States, 94143

Contacts

Stanford

Recruiting

Stanford, California, United States, 94305

Contacts

University of Colorado Anschutz

Recruiting

Aurora, Colorado, United States, 80045

Contacts

University of Colorado

Recruiting

Denver, Colorado, United States, 80204

Contacts

Moffitt Cancer Center

Recruiting

Tampa, Florida, United States, 87535

Contacts

Dana Farber

Recruiting

Boston, Massachusetts, United States, 02215

Contacts

University of New Mexico

Recruiting

Albuquerque, New Mexico, United States, 87106

Contacts

UPenn

Recruiting

Philadelphia, Pennsylvania, United States, 19107

Contacts

More Information

Sponsor

Linnaeus Therapeutics, Inc.

Last update posted

Apr 22, 2026

Last verified

Sep, 2025

Keywords

  • Melanoma

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Linnaeus Therapeutics, Inc. on 2026-04-22.