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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Anlotinib

for Alveolar Soft Part Sarcoma

THIS STUDY IS CURRENTLY RECRUITING PATIENTS WITH ALVEOLAR SOFT PART SARCOMA ONLY AND IS NO LONGER RECRUITING PATIENTS WITH SYNOVIAL SARCOMA OR LEIOMYOSARCOMA. This study evaluates the safety and efficacy of AL3818 (anlotinib) hydrochloride in the treatment of metastatic or advanced alveolar soft part sarcoma (ASPS), leiomyosarcoma (LMS), and synovial sarcoma (SS). All participants with ASPS will receive open-label AL3818. In participants with LMS or SS, AL3818 will be compared to IV dacarbazine. Two-thirds of the participants will receive AL3818, one-third of the participants will receive IV dacarbazine.

Recruiting

1 award

Phase 3

More about Bartosz Chmielowski, MD

Clinical Trial Related

4 years of experience running clinical trials · Led 19 trials as a Principal Investigator · 5 Active Clinical Trials

Treatments Bartosz Chmielowski, MD has experience with

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

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