Bartosz Chmielowski, MD - Sarcoma and ...

Dr. Bartosz Chmielowski, MD

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UCLA

Expert in Melanoma
Studies Skin Cancer
19 reported clinical trials
33 drugs studied

Area of expertise

1

Melanoma

Global Leader

Bartosz Chmielowski, MD has run 13 trials for Melanoma. Some of their research focus areas include:

Stage IV
BRAF positive
Stage III
2

Skin Cancer

Bartosz Chmielowski, MD has run 7 trials for Skin Cancer. Some of their research focus areas include:

Stage IV
BRAF positive
Stage III

Affiliated Hospitals

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UCLA

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University Of California, Los Angeles

Clinical Trials Bartosz Chmielowski, MD is currently running

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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.

Recruiting

1 award

Phase 1 & 2

9 criteria

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GIM-122

for Advanced Solid Cancers

GIM-122 is a first-in-class, humanized immunoglobulin G1 kappa dual functioning monoclonal antibody (DFA). This phase 1 / 2 study plans to evaluate the safety, tolerability, pharmacokinetics and clinical efficacy of intravenous (IV) administration of GIM-122 in adults with advanced malignancies.

Recruiting

1 award

Phase 1 & 2

9 criteria

More about Bartosz Chmielowski, MD

Clinical Trial Related

4 years of experience running clinical trials · Led 19 trials as a Principal Investigator · 4 Active Clinical Trials

Treatments Bartosz Chmielowski, MD has experience with

  • Nivolumab
  • Pembrolizumab
  • Ipilimumab
  • Dacarbazine
  • IDE196
  • Binimetinib

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