Marlana M Orloff MD | Jefferson Health

Dr. Marlana Orloff, MD

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Thomas Jefferson University

Studies Eye Cancer
Studies Uveal Melanoma
10 reported clinical trials
19 drugs studied

Area of expertise

1Eye Cancer
Marlana Orloff, MD has run 9 trials for Eye Cancer. Some of their research focus areas include:
Stage IV
HLA-A negative
GNAQ positive
2Uveal Melanoma
Marlana Orloff, MD has run 8 trials for Uveal Melanoma. Some of their research focus areas include:
Stage IV
HLA-A negative
GNAQ positive

Affiliated Hospitals

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Thomas Jefferson University
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Thomas Jefferson University Hospital

Clinical Trials Marlana Orloff, MD is currently running

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Darovasertib + Crizotinib

for Uveal Melanoma

This trial is testing a new drug combination (IDE196 and crizotinib) on patients with a specific type of eye cancer that has spread. The goal is to see if this combination can stop or slow down the cancer better than other treatments. Crizotinib has been used in treating various cancers with ALK gene rearrangements, showing high response rates.
Recruiting1 award Phase 2 & 38 criteria
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IDE196 Combinations

for Solid Tumors

This is a Phase 1/2, multi-center, open-label basket study designed to evaluate the safety and anti-tumor activity of IDE196 in patients with solid tumors harboring GNAQ or GNA11 (GNAQ/11) mutations or PRKC fusions, including metastatic uveal melanoma (MUM), cutaneous melanoma, colorectal cancer, and other solid tumors. Phase 1 (dose escalation - monotherapy) will assess safety, tolerability and pharmacokinetics of IDE196 via standard dose escalation scheme and determine the recommended Phase 2 dose. Safety and anti-tumor activity will be assessed in the Phase 2 (dose expansion) part of the study. Phase 1 (dose escalation - binimetib combination) will assess safety, tolerability and pharmacokinetics of IDE196 and binimetinib via standard dose escalation scheme and determine the recommended Phase 2 dose. Safety and anti-tumor activity will be assessed in the Phase 2 (dose expansion) part of the study. Phase 1 (dose escalation - crizotinib combination) will assess safety, tolerability and pharmacokinetics of IDE196 and crizotinib via standard dose escalation scheme and determine the recommended Phase 2 dose. Safety and anti-tumor activity will be assessed in the Phase 2 (dose expansion) part of the study. Evaluation of safety and efficacy across multiple doses may be explored in the dose optimization part of the study. Crizotinib monotherapy with crossover to combination cohort may be assessed for safety and to show the contribution of each study drug to anti-tumor activity. As of Protocol Amendment 10, Phase 1, Phase 2 dose expansion in IDE196 monotherapy, and Phase 2 dose expansion of IDE196 in combination with binimetinib have been fully enrolled. There were no patients enrolled in the crizotinib monotherapy cohorts.
Recruiting1 award Phase 1 & 29 criteria

More about Marlana Orloff, MD

Clinical Trial Related2 years of experience running clinical trials · Led 10 trials as a Principal Investigator · 4 Active Clinical Trials
Treatments Marlana Orloff, MD has experience with
  • Pembrolizumab
  • IDE196
  • Crizotinib
  • Ipilimumab
  • Nivolumab
  • SD-101

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