Melanoma Research Institute of Excellence

Contact

Name: Mitchell Berkowitz
Position: Program Manager
Organization: Melanoma Research Institute of Excellence
Contact Number(s):

Contact

Name: Shingo Sato
Position:
  • Associate Program Manager
  • Director of Database Design and Utilization
Organization: Melanoma Research Institute of Excellence
Contact Number(s):

Clinical Trials

Marlana Orloff, MD

Principal Investigator

Takami Sato, MD, PhD

Principal Investigator

Rino Seedor, MD

Principal Investigator

A Multicenter, Randomized, Double-Blind Phase 3 Study of HBI-8000 Combined with Nivolumab versus Placebo with Nivolumab in Patients with Unresectable or Metastatic Melanoma Not Previously Treated with PD-1 or PD-L1 Inhibitors
Phase 2/3 Randomized Study of Tebentafusp as Monotherapy and in Combination with Pembrolizumab Versus Investigator s Choice in HLA-A*02:01-positive Participants with Previously Treated Advanced Melanoma
A Phase I/II Study of Tebentafusp-tebn in Combination with Liver-Directed Therapies for the Treatment of Metastatic Uveal Melanoma
Neoadjuvant Tebentafusp in Patients with Locally Advanced, Unresectable Primary Uveal Melanoma
A Phase II Study of Biomarker Driven Early Discontinuation of Anti-PD-1 Therapy in Patients With Advanced Melanoma (PET-Stop)
A Phase 3 Randomized, Controlled Study of IMC-F106C Plus Nivolumab Versus Nivolumab Regimens in HLA-A*02:01-Positive Participants With Previously Untreated Advanced Melanoma (PRISM-MEL-301)
A Phase 2 Peri-Operative Trial of Fianlimab and Cemiplimab Compared With Anti-PD1 Alone in Patients With Resectable Stage III and IV Melanoma
A Randomized, Controlled, Multicenter, Phase 3 Clinical Study Comparing Vusolimogene Oderparepvec in Combination with Nivolumab Versus Treatment of Physician's Choice in Patients with Advanced Melanoma That Has Progressed on an Anti-PD-1 and an Anti-CTLA-4 Containing Treatment Regimen [IGNYTE-3]
A prospective, multicenter, open-label, randomized, actively controlled, parallel-group Phase 3 clinical trial to evaluate efficacy, safety, and tolerability of IMA203 versus investigator's choice in patients with previously treated, unresectable or metastatic cutaneous melanoma (ACTengine® IMA203-301)
Phase 1/2 study evaluating genetically modified autologous T cells expressing a T-cell receptor recognizing a cancer/germline antigen as monotherapy or in combination with nivolumab in patients with recurrent and/or refractory solid tumors (ACTengine® IMA203-101)
A Randomized Phase III Study of Management of Treatment Naive Primary Melanoma in Elderly Patients (EA6244)
Clinical Research Staff