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Terminated Phase 2 Interventional Results available

Safety and Efficacy of Selinexor in Combination With Pembrolizumab in Recurrent Advanced Melanoma

ClinicalTrials.gov ID: NCT04768881

Public ClinicalTrials.gov record NCT04768881. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 8, 2026, 2:59 AM EST

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Official title

A Phase 2 Open-Label Multicenter Study to Evaluate the Safety and Efficacy of Selinexor in Combination With Pembrolizumab in Recurrent Advanced Melanoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Approximately 40 participants with locally advanced or metastatic melanoma will be enrolled in 20 sites in the United States into 1 of the following 2 arms: Primary resistance to initial checkpoint inhibitor (CPI) therapy in Arm A and Acquired resistance to initial CPI therapy in Arm B. Participants who have disease progression (PD) after discontinuation of CPIs, especially in neoadjuvant or adjuvant therapy, will be considered to have acquired resistance in this study. Participants will receive study treatment (Selinexor and Pembrolizumab) until PD, intolerable toxicity or withdrawal from the study, whichever occurs first.

Study identification

NCT ID
NCT04768881
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Karyopharm Therapeutics Inc
Industry
Enrollment
15 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 12, 2021 (Actual)
Primary completion
Sep 22, 2023 (Actual)
Completion
Sep 22, 2023 (Actual)
Last update posted
Aug 23, 2024

2021 – 2023

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
13
Facility City State ZIP Site status
UCLA Los Angeles California 90095 —
TOI Clinical Research Pasadena California 91105 —
BRCR Global Plantation Florida 33322 —
Minnesota Oncology Hematology Minneapolis Minnesota 55404 —
Great Plains Health North Platte Nebraska 69101 —
John Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08901 —
New York Oncology Hematology Albany New York 12206 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
OH Care Clinical Trials Cincinnati Ohio 45242 —
Cleveland Clinic Foundation Cleveland Ohio 44144 —
Texas Oncology-Austin Central Austin Texas 78731 —
Texas Oncology - Baylor Sammons Center Dallas Texas 75246 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04768881, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 23, 2024 · Synced Nov 8, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04768881 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →