Skip to main content
Clinical Trials/NCT04607889
NCT04607889
Completed
Not Applicable

Measurement of Patient Views on the Attributes of Cancer Genomic Medicine in Japan (Patient View Study)

Bayer1 site in 1 country605 target enrollmentDecember 15, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer Genomic Profiling
Sponsor
Bayer
Enrollment
605
Locations
1
Primary Endpoint
Best-Worst Scaling scores showing patient preferences for the attributes of the process of taking panel tests
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Researchers are looking for a better way to treat people with solid tumors. One new way is called cancer genomic medicine. In cancer genomic medicine, doctors use tests to look at the genetic information in a solid tumor. These tests are called panel tests. The results of the panel tests help doctors to choose the best type of medicine to treat that tumor.

In this study, the researchers want to learn more about what a large number of patients with solid tumors think are the burden and benefits of taking panel tests. The researchers also want to know what doctors who treat patients with solid tumors think about panel tests.

The study will include about 650 men and women in Japan who are at least 20 years old. About 340 of the participants will be patients with solid tumors who are taking medicine to help treat their tumors. About 310 of the patients will be doctors who are treating patients with solid tumors.

There will be 3 parts in this study. Part 1 will include patients with solid tumors. Parts 2 and 3 will include patients with solid tumors and doctors who are treating patients with solid tumors. In each part, the patients and doctors will answer questions about what they think of panel tests. During Part 1, all of the patients will answer questions in a teleconference. Some of the patients and physicians in Part 2 will also answer questions in a teleconference. During Part 2 and Part 3, all of the patients and doctors will complete an online questionnaire.

Registry
clinicaltrials.gov
Start Date
December 15, 2020
End Date
September 15, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Bayer
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult female or male patient
  • Diagnosis of a solid tumor
  • Patients familiar with panel tests to be defined as:
  • Patients who have taken a panel test
  • Patients who have not taken a panel test
  • Patients who have tried or considered taking a panel test
  • Patients who have been offered a panel test but refused
  • Signed informed consent
  • Is 20 years of age or older
  • Part 2 and Part 3 (patients):

Exclusion Criteria

  • Non-Japanese speakers
  • Declaring to be too unwell to perform an interview
  • Part2 and Part 3 (patients):
  • Non-Japanese speakers
  • Declaring to be too unwell to complete the survey
  • Participation in the pilot study
  • Part 2 and Part 3 (physician):
  • Non-Japanese speakers

Outcomes

Primary Outcomes

Best-Worst Scaling scores showing patient preferences for the attributes of the process of taking panel tests

Time Frame: Up to 25 minutes

Respondents will choose "Best" or "Worst" for prepared questions.

Secondary Outcomes

  • Ranking of Best-Worst scaling scores for patients and for doctors(Up to 25 minutes)
  • Best-Worst Scaling scores showing doctor preferences for the attributes of the process of taking panel tests(Up to 25 minutes)
  • Patient and doctor willingness to try/offer panel tests based on different hypothetical conditions of panel tests and drugs in cancer genomic medicine(Up to 25 minutes)

Study Sites (1)

Loading locations...

Similar Trials

Completed
Phase 2
A Trial to Learn Whether Regorafenib in Combination With Nivolumab Can Improve Tumor Responses and How Safe it is for Participants With Solid TumorsSolid Tumors
NCT04704154Bayer175
Active, not recruiting
Phase 1
A First-in-human Study to Learn How Safe the Study Drug BAY2965501 is, Find the Best Dose (Single Drug & Combination), How it Affects the Body, What Maximum Amount Can be Given, How it Moves Into, Through and Out of the Body, How it Acts on Different Tumors in Participants With Advanced Solid TumorsAdvanced Solid Tumors
NCT05614102Bayer284
Completed
Phase 1
A first-in-human study to learn how safe the study treatment BAY2862789 is, to find the best dose, how it affects the body, what maximum amount can be given, how it moves into, through and out of the body, and how it acts on different tumors in participants with advanced solid tumors
2024-510998-26-00Bayer AG45
Terminated
Phase 1
A Study to Learn How Safe BAY2666605 is, How it Affects the Body, How it Moves Into, Through and Out of the Body, the Maximum Amount That Can be Given and Its Action Against Tumors in Adult Participants With Skin Cancer That Has Spread to Other Parts of the Body and Other Types of Advanced CancerMetastatic Melanoma and Other Solid Tumors
NCT04809805Bayer5
Active, not recruiting
Phase 1
A First-in-human Study to Learn How Safe the Study Drug BAY3375968, an Anti-CCR8 Antibody, is, When Given Alone or in Combination With Pembrolizumab, How it Affects the Body, How it Moves Into, Through, and Out of the Body, and to Find the Best Dose in Participants With Advanced Solid TumorsAdvanced Solid Tumors
NCT05537740Bayer129