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Study record managers: refer to the Data Element Definitions if submitting registration or information. Phase II.


Study record managers: refer to the Data Element Definitions if submitting registration or information. Phase II.

To evaluate the frequency and severity of toxicities associated with GDC To identify potential resistance biomarkers at disease progression. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Upon progression, patients may be eligible to re-register to Caht III. Talk with your doctor and family members or friends about deciding to a study.

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To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Hide glossary Glossary Study record managers: refer to the Data Element Definitions escort agents mandurah submitting registration or information. Search for terms x. COVID is an emerging, rapidly evolving situation. Save this study. Warning You have reached the maximum of saved studies Listing a study does not mean it has chaf evaluated by the U.

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Federal Government. Read our disclaimer for details. First Posted : March 6, Last Update Posted : October 23, Study Description. This phase II trial studies how well taselisib GDC works in treating patients with stage IV squamous cell lung cancer that has come back after treatment.

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This is a sub-study that includes all screened patients positive for the phosphoinositide 3-kinase PI3K biomarker. PI3K can cause tumor cells to grow more quickly. Taselisib may decrease the activity of PI3K and may be able to shrink tumors. Show detailed description.

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Hide detailed description. Detailed Description:. Phase II II. Phase II IV. FDA Resources. Arms and Interventions.

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Outcome Measures. From date of sub-study registration to date of death due to any cause assessed by local review. Among participants who had a response, duration is calculated from registration to response date. Frequency and severity of toxicities greater than Grade 2 associated with GDC Eligibility Criteria.

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Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the carolona research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.

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More Information. National Library of Medicine U. National Institutes of Health U.

Department of Health and Human Services. The kjng and scientific validity of this study is the responsibility of the study sponsor and investigators. Phase 2. Study Type :. Actual Enrollment :.

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Actual Study Start Date :. Actual Primary Completion Date :. Actual Study Completion Date :.

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