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Available clinical trials are below. Click the + sign to expand and review details about their purpose, eligibility criteria, and contact information for study staff. For some studies, you will find a link to ClinicalTrials.gov, where you can explore more information about each study.

ECOG-ACRIN - EA6141

Study Phase: Phase II/III, Drug

Condition(s): Stage III or IV melanoma
Randomized Phase II/III Study of Nivolumab plus Ipilimumab plus Sargramostim versus Nivolumab plus Ipilimumab in Patients with Unresectable Stage III or Stage IV Melanoma

ClinicalTrials.gov NCT ID: NCT02339571

You can view the full clinical description on ClinicalTrials.gov.

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profile_amy-grossman

Amy Grossman, RN

Primary Contact - Study Coordinator


484-658-1788
amy.grossman@sluhn.org

profile_melissa-wilson

Melissa A. Wilson, MD, PhD

Physician - Principal Investigator


Regeneron - R3767-ONC-22122

Study Phase: Phase III - Drug

Condition(s): Unresectable or metastatic melanoma
A Phase 3 Study Of Fixed Dose Combinations Of Fianlimab And Cemiplimab Versus Relatlimab And Nivolumab In Participants With Unresectable Or Metastatic Melanoma

ClinicalTrials.gov NCT ID: NCT06246916

You can view the full clinical description on ClinicalTrials.gov.

View Full Description
profile_amy-grossman

Amy Grossman, RN

Primary Contact - Study Coordinator


484-658-1788
amy.grossman@sluhn.org

profile_melissa-wilson

Melissa A. Wilson, MD, PhD

Physician - Principal Investigator


Iovance - IOV-MEL-301

Study Phase: Phase III - Drug

Condition(s): Unresectable or metastatic melanoma
A Phase 3, multicenter, randomized, open-label, parallel group, treatment study to assess the efficacy and safety of the lifileucel (LN-144, autologous tumor-infiltrating lymphocytes [TIL]) regimen in combination with pembrolizumab compared with pembrolizumab monotherapy in participants with untreated, unresectable or metastatic melanoma

ClinicalTrials.gov NCT ID: NCT 05727904

You can view the full clinical description on ClinicalTrials.gov.

View Full Description
profile_amy-grossman

Amy Grossman, RN

Primary Contact - Study Coordinator


484-658-1788
amy.grossman@sluhn.org

profile_melissa-wilson

Melissa A. Wilson, MD, PhD

Physician - Principal Investigator


U of Kentucky - UKY-MCC-20-MEL-11-PMC

Study Phase: Phase I - Drug

Condition(s): BRAF mutated metastatic melanoma
A Phase I Study of Nilotinib in Combination with Dabrafenib and Trametinib in BRAF V600 Mutant Metastatic Melanoma after Progression on BRAF/MEK Inhibition

ClinicalTrials.gov NCT ID: NCT04903119

You can view the full clinical description on ClinicalTrials.gov.

View Full Description
profile_amy-grossman

Amy Grossman, RN

Primary Contact - Study Coordinator


484-658-1788
amy.grossman@sluhn.org

profile_melissa-wilson

Melissa A. Wilson, MD, PhD

Physician - Principal Investigator


To inquire if you're eligible for a clinical trial, contact: (484) 658-5080, or click here to complete a clinical trial inquiry form.

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