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临床试验/NCT05693831
NCT05693831招募中不适用

myCare-102: A Survey of Physician and Molecular Tumor Board Perspectives on the Clinical Utility and Usability of Cellworks Singula™ and Cellworks Ventura™ Reports in Facilitating Patient Treatment Decisions for Pan-Cancer Patients

Cellworks Group Inc.1 个研究点 分布在 1 个国家目标入组 730 人开始时间: 2022年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
730
试验地点
1
主要终点
Surveyed View of Cellworks Singula and Ventura™ reports

研究概览

简要总结

The purpose of this study is to determine the benefit of Cellworks Singula™ reports on physician and molecular tumor board treatment recommendations across a large set of pan-cancer indications who have already received first-line therapy. The study is also to determine the benefit of Cellworks Ventura™ reports on physician and molecular tumor board treatment recommendations across a large set of relapsed or refractory pan-cancer indications.

The primary objective of this study is to survey physicians and molecular tumor board perspectives of the benefit of Cellworks Singula™and Cellworks Ventura™ reports in facilitating treatment decisions in pan-cancer patients.

Cellworks reports aim to provide NGS-based therapy recommendations to aid the decision-making of patients, physicians, and molecular tumor boards. Cellworks reports aim to provide NGS-based therapy recommendations to aid the decision-making of patients, physicians, and molecular tumor boards.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Have cancer for the indications listed at: https://cellworks.life/mycare
  • Patients are eligible at any stage of the disease.
  • Have already received first-line therapy
  • For Cellworks Singula™ report, patients must be Relapsed or refractory after first-line treatment.
  • For Cellworks Ventura™ report, patients must have relapsed or refractory cancer and have exhausted standard of care therapy options
  • Expected to be alive 6 months or more
  • Requirements for NGS testing (e.g., panel or whole-exome sequencing)
  • NGS testing has been ordered from or performed by one or more vendors specified at: https://cellworks.life/mycare102
  • NGS reports must be ordered or performed within the last 90 days
  • Cellworks will accept all NGS input formats available, including PDF, VCF, BAM, and FastQ.
  • Requirements for additional laboratory testing: If Hematological Indication then Cytogenetics in the form of FISH, Karyotyping, IHC, and/or aCGH has been ordered. If Acute Myeloid Leukemia (AML) then FLT3-itd testing has been ordered. If the Indication is a form of Brain Cancer (e.g., glioblastoma) then Cytogenetics in the form of FISH, Karyotyping, IHC, and/or aCGH has been ordered and MGMT Methylation test has been ordered.

排除标准

  • Patients not previously diagnosed with cancer of any of the indications listed at: https://cellworks.life/mycare102
  • Patients without an NGS report ordered/performed within the past 90 days
  • Patients who are expected to be alive less than 6 months
  • Pregnant women
  • Patients who have not exhausted standard-of-care treatment options or who have known effective therapy
  • Patients that fall into the following categories based on survey response will considered excluded from eligibility: If recommendations were made before receiving the Cellworks report, patients will not be included in the primary analysis but will be included in the ITT analysis. If recommended an FDA approved therapy that was not included on the Cellworks report. If recommended a clinical trial for a therapy that was not included in the Cellworks report. If the therapy/therapies on the Cellworks report was/were not covered by the patient's insurance. If the therapy/therapies on the Cellworks report was/were too expensive.

结局指标

主要结局

Surveyed View of Cellworks Singula and Ventura™ reports

时间窗: Approximately 24 months

Majority of physicians and molecular tumor boards (MTB) have a positive view of the Cellworks Singula™ and Cellworks Ventura™ reports

次要结局

  • Patient Demographics (Sex)(Approximately 24 months)
  • Patient Disease Status (Indication)(Approximately 24 months)
  • Patient Disease Status (ECOG)(Approximately 24 months)
  • Patient Demographics (Ethnicity)(Approximately 24 months)
  • Institution Demographics (Orders Placed)(Approximately 24 months)
  • Institution Demographics (Placement of Orders)(Approximately 24 months)
  • Patient Demographics (Age)(Approximately 24 months)
  • Institution Demographics (Type)(Approximately 24 months)

研究者

发起方
Cellworks Group Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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