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Patient Feasibility
Next-level trials: Beyond sites
At the intersection of technology and human experience lies Patient Feasibility – a structured process underpinned by tools that capture, store, and generate patient insights for a 360° clinical trial planning.
At the intersection of technology and human experience lies Patient Feasibility – a structured process underpinned by tools that capture, store, and generate patient insights for a 360° clinical trial planning.
Start with the patient pathway
98%
Accuracy in linking reimbursed drugs to their indications.
Locate eligible patients. Determine countries where the patient pathway aligns with your protocol specifics – see where your specified drug is reimbursed and is part of the SoC.
Pinpoint obstacles and possibilities in recruitment.
Patients benefiting from a high SoC often lack the incentive to join clinical trials.
Understand the burden of participation. Compare your trial protocol to the local SoC to spot areas of similarity and potential barriers. The more familiar your protocol is to patients, the lower your drop out rate is likely to be.
Map out the patient pathway. And see where your trial fits in. Insights about reimbursed drugs and their application together with TH’s AI-powered chat can paint a picture of your patients’ journey from first symptoms to treatment.
Understand the patient pathway in every location by comparing your protocol to the local Standard of Care. Identify both the incentives and the barriers to participation patients can encounter in your trial.
And don’t stop there. Get equipped with data on the scenarios and conditions these drugs are reimbursed and you will have half of the patient pathway in hand.
Start with the patient pathway
98%
Accuracy in linking reimbursed drugs to their indications.
Locate eligible patients. Determine countries where the patient pathway aligns with your protocol specifics – see where your specified drug is reimbursed and is part of the SoC.
Pinpoint obstacles and possibilities in recruitment.
Patients benefiting from a high SoC often lack the incentive to join clinical trials.
Understand the burden of participation. Compare your trial protocol to the local SoC to spot areas of similarity and potential barriers. The more familiar your protocol is to patients, the lower your drop out rate is likely to be.
Map out the patient pathway. And see where your trial fits in. Insights about reimbursed drugs and their application together with TH’s AI-powered chat can paint a picture of your patients’ journey from first symptoms to treatment.
Understand the patient pathway in every location by comparing your protocol to the local Standard of Care. Identify both the incentives and the barriers to participation patients can encounter in your trial.
And don’t stop there. Get equipped with data on the scenarios and conditions these drugs are reimbursed and you will have half of the patient pathway in hand.
AI to gain profound patient insights
Stand on the shoulders of decades of medical research
Put your ever-growing data into practical use, derive invaluable insights, get ahead of the competition.
With TrialHub IQ, you can generate highly accurate patient insights in a matter of seconds. The expensive market research you we planning to conduct – may not be needed anymore.
And there is more:
The most precious information may reside in your own company data. The hundreds of texts or spreadsheets, data in any format that you’ve accumulated over the years and are a nightmare to manually search through.
Use TrialHub IQ to:
- Securely upload your proprietary data
- Combine your data together with TrialHub’s data
- Get unique insights and trace them back to the sources
AI to gain profound patient insights
Stand on the shoulders of decades of medical research
With TrialHub IQ, you can generate highly accurate patient insights in a matter of seconds. The expensive market research you we planning to conduct – may not be needed anymore.
And there is more:
The most precious information may reside in your own company data. The hundreds of texts or spreadsheets, data in any format that you’ve accumulated over the years and are a nightmare to manually search through.
Use TrialHub IQ to:
- Securely upload your proprietary data
- Combine your data together with TrialHub’s data
- Get unique insights and trace them back to the sources
TrialHub helped Boehringer Ingelheim
systematize patient data capture & storage
Boehringer Ingelheim’s goal was to systematize the capture, storage, and access of patient insights for future clinical development. As a pivotal part of this project, they collaborated with TrialHub.
Thanks to our AI-powered technology, BI could instantly tap into comprehensive patient insights, site feedback, and extensive in-house knowledge, thereby refining and enhancing their patient-centric trial designs from a vast array of sources.
TrialHub helped Boehringer Ingelheim systematize patient data capture & storage
Boehringer Ingelheim’s goal was to systematize the capture, storage, and access of patient insights for future clinical development. As a pivotal part of this project, they collaborated with TrialHub.
Thanks to our AI-powered technology, BI could instantly tap into comprehensive patient insights, site feedback, and extensive in-house knowledge, thereby refining and enhancing their patient-centric trial designs from a vast array of sources.
#PatientsFirst
Patient inclusion through education
Patient understanding is key to engaging underserved and diverse populations, a critical objective in today’s industry.
Proudly, we advocate a #PatientsFirst approach and invite you to join our mission.
TrialHub’s parent company, FindMeCure, offers a free platform where patients can find trials, suitable for their needs and conditions. Through FindMeCure, we support patients in their trial-searching journey and understand their needs along the way.
We go beyond that, with you.
By partnering with TrialHub, every client donates a full scholarship to the European Patients’ Academy on Therapeutic Innovation (EUPATI) which covers an education course for a single patient.
Designing successful clinical trials starts and ends with the patients. Patient Feasibility is the bridge. Cross it, and understand your target audience.
#PatientsFirst
Patient inclusion through education
Patient understanding is key to engaging underserved and diverse populations, a critical objective in today’s industry.
Proudly, we advocate a #PatientsFirst approach and invite you to join our mission.
TrialHub’s parent company, FindMeCure, offers a free platform where patients can find trials, suitable for their needs and conditions. Through FindMeCure, we support patients in their trial-searching journey and understand their needs along the way.
We go beyond that, with you.
By partnering with TrialHub, every client donates a full scholarship to the European Patients’ Academy on Therapeutic Innovation (EUPATI) which covers an education course for a single patient.
Designing successful clinical trials starts and ends with the patients. Patient Feasibility is the bridge. Cross it, and understand your target audience.
See our other use cases that make
the perfect 360° feasibility assessment
TrialHub was born out of the need to address the challenges Feasibility teams face when they design their clinical trials. Today, TrialHub is more than just a feasibility platform. It goes beyond Site and Country Feasibility to give its users access to the missing link – Patient Feasibility.
Country Feasibility
TrialHub’s Feasibility Index helps you select the best countries for your clinical trial based on your recruitment goals in terms of:
- Epidemiology
- Competition
- Past experience (Completed trials)
- Average recruitment rates
- Startup timelines
Site Feasibility
TrialHub helps you identify the best sites for your clinical trial so you complete patient recruitment on budget and on time by assessing:
- Past experience and current clinical trials data
- Site performance statistics and recruitment delays
- Site recommendations from local industry experts
- Patients around the site
Country Feasibility
- Epidemiology
- Competition
- Past experience (completed trials)
- Average recruitment rates
- Startup timelines
Site Feasibility
- Past experience and current clinical trials data
- Site performance statistics and recruitment delays
- Site recommendations from local industry experts
- Patients around the site
Empowering the Clinical Trials of Tomorrow.
Analyze. Design. Revolutionize.
