Neoadjuvant Combination Immunotherapy for Stage III Melanoma

Recruiting Phase 2 Interventional Study
Cutaneous Melanoma
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Other
Participants needed
28 (estimated)
Sponsor
University of Louisville · Other
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About This Trial

Determine safety and efficacy of pre-operative combination immunotherapy with Talimogene Laherparepvec (T-VEC)/Pembrolizumab given prior to complete lymph node dissection in resectable stage 3 cutaneous melanoma with clinically apparent lymph node metastases.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 18 years of age, any race or sex, who have pathologically confirmed cutaneous melanoma * ECOG performance status of 0 or 1 * Adequate hematologic, hepatic, renal and coagulation function * Must have measurable disease and have an injectable target lymph node for intralesional …
Contacts

Michael Egger, MD

502-629-6950

michael.egger@louisville.edu

CONTACT