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Last Updated: April 18, 2024

CLINICAL TRIALS PROFILE FOR PREXASERTIB


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Clinical Trials for Prexasertib

Trial ID Title Status Sponsor Phase Summary
NCT01115790 ↗ A Phase 1 Study in Participants With Advanced Cancer Completed Eli Lilly and Company Phase 1 The primary purpose of Parts A and B of this study is to evaluate the safety and toxicity of prexasertib (an inhibitor of checkpoint kinase 1[chk 1]) in participants with advanced or metastatic cancer (Part A), or squamous cell cancer of the head and neck or squamous cell cancer of any tumor type (Part B). Part C of the study will evaluate prexasertib in three different groups of participants; those with squamous cell cancer of the head and neck that has recurred or spread to other parts of the body, those with squamous non-small cell lung cancer that has recurred or spread, and those with squamous cell cancer of the anus that is not curable by existing therapy.
NCT02124148 ↗ A Study of Prexasertib (LY2606368) With Chemotherapy or Targeted Agents in Participants With Advanced Cancer Completed Eli Lilly and Company Phase 1 The main purpose of this study is to investigate the safety of prexasertib in combination with other anti-cancer drugs (cisplatin, cetuximab, pemetrexed, fluorouracil or LY3023414) in participants with advanced cancer or cancer that has spread to another part of the body. The study has multiple parts (A, B, C, D and E). Participants will only enroll in one part.
NCT02514603 ↗ A Study of Prexasertib (LY2606368) in Japanese Participants With Advanced Cancers Completed Eli Lilly and Company Phase 1 The primary purpose of this study is to assess the tolerability of prexasertib in Japanese participants with advanced solid cancers.
NCT02555644 ↗ A Study of Prexasertib (LY2606368) With Chemotherapy and Radiation in Participants With Head and Neck Cancer Completed Eli Lilly and Company Phase 1 The main purpose of this study is to investigate the safety of prexasertib in combination with other anti-cancer drugs (cisplatin or cetuximab) and radiation therapy in participants with locally advanced head and neck cancer. The study has two parts (A and B). Participants will only enroll in one part.
NCT02649764 ↗ Prexasertib (LY2606368), Cytarabine, and Fludarabine in Patients With Relapsed or Refractory Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome Active, not recruiting Eli Lilly and Company Phase 1 This phase I trial studies the side effects and determine the best dose of prexasertib (LY2606368) when given together with cytarabine and fludarabine in patients with acute myeloid leukemia or high-risk myelodysplastic syndrome that has returned after a period of improvement or no longer responds to treatment. Prexasertib (LY2606368) may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cytarabine and fludarabine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving prexasertib (LY2606368) together with cytarabine and fludarabine may work better in treating patients with acute myeloid leukemia or myelodysplastic syndrome.
NCT02649764 ↗ Prexasertib (LY2606368), Cytarabine, and Fludarabine in Patients With Relapsed or Refractory Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome Active, not recruiting National Cancer Institute (NCI) Phase 1 This phase I trial studies the side effects and determine the best dose of prexasertib (LY2606368) when given together with cytarabine and fludarabine in patients with acute myeloid leukemia or high-risk myelodysplastic syndrome that has returned after a period of improvement or no longer responds to treatment. Prexasertib (LY2606368) may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cytarabine and fludarabine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving prexasertib (LY2606368) together with cytarabine and fludarabine may work better in treating patients with acute myeloid leukemia or myelodysplastic syndrome.
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for Prexasertib

Condition Name

Condition Name for
Intervention Trials
Advanced Cancer 3
CNS Cancer 1
Solid Tumor 1
Medulloblastoma Recurrent 1
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Condition MeSH

Condition MeSH for
Intervention Trials
Neoplasms 8
Leukemia, Myeloid 2
Syndrome 2
Carcinoma, Ovarian Epithelial 2
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Clinical Trial Locations for Prexasertib

Trials by Country

Trials by Country for
Location Trials
United States 64
United Kingdom 8
Australia 4
Italy 4
Korea, Republic of 3
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Trials by US State

Trials by US State for
Location Trials
Massachusetts 7
Tennessee 7
Texas 7
Florida 5
Ohio 3
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Clinical Trial Progress for Prexasertib

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 2 4
Phase 1/Phase 2 2
Phase 1 12
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Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Completed 11
Recruiting 4
Active, not recruiting 2
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Clinical Trial Sponsors for Prexasertib

Sponsor Name

Sponsor Name for
Sponsor Trials
Eli Lilly and Company 14
Dana-Farber Cancer Institute 3
National Cancer Institute (NCI) 2
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Sponsor Type

Sponsor Type for
Sponsor Trials
Industry 16
Other 11
NIH 2
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