Daniel Olson, MD - UChicago Medicine

Dr. Daniel Olson, MD

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University of Chicago Comprehensive Cancer Center

Studies Skin Cancer
Studies Liposarcoma
9 reported clinical trials
15 drugs studied

Area of expertise

1Skin Cancer
Daniel Olson, MD has run 3 trials for Skin Cancer. Some of their research focus areas include:
Stage IV
Stage III
Stage I
2Liposarcoma
Daniel Olson, MD has run 2 trials for Liposarcoma. Some of their research focus areas include:
Stage IV

Affiliated Hospitals

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University Of Chicago Comprehensive Cancer Center
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UC Comprehensive Cancer Center At Silver Cross

Clinical Trials Daniel Olson, MD is currently running

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Immunotherapy + Chemotherapy

for Sarcoma

This phase III trial compares the effect of immunotherapy (pembrolizumab) plus chemotherapy (doxorubicin) to chemotherapy (doxorubicin) alone in treating patients with dedifferentiated liposarcoma (DDLPS), undifferentiated pleomorphic sarcoma (UPS) or a related poorly differentiated sarcoma that has spread from where it first started (primary site) to other places in the body (metastatic) or that cannot be removed by surgery (unresectable). Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's deoxyribonucleic acid (DNA) and may kill tumor cells. It also blocks a certain enzyme needed for cell division and DNA repair. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Adding immunotherapy (pembrolizumab) to the standard chemotherapy (doxorubicin) may help patients with metastatic or unresectable DDLPS, UPS or a related poorly differentiated sarcoma live longer without having disease progression.
Recruiting2 awards Phase 310 criteria
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INBRX-106 + Pembrolizumab

for Lung Cancer

This is a Phase 1/2, open-label, non-randomized, 4-part trial to determine the safety profile and identify the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of INBRX 106 administered as a single agent or in combination with the anti-PD-1 checkpoint inhibitor (CPI) pembrolizumab (Keytruda®). KEYTRUDA is a registered trademark of Merck Sharp \& Dohme LLC, a subsidiary of Merck \& Co., Inc., Rahway, NJ, USA.
Recruiting1 award Phase 1 & 25 criteria

More about Daniel Olson, MD

Clinical Trial Related3 years of experience running clinical trials · Led 9 trials as a Principal Investigator · 3 Active Clinical Trials
Treatments Daniel Olson, MD has experience with
  • Pembrolizumab
  • TAC01-HER2
  • Paclitaxel
  • Nivolumab
  • Doxorubicin
  • Pegylated Liposomal Doxorubicin Hydrochloride

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