myMedidata

患者が臨床試験に参加する場合、試験の運用にそって多くのものを求められます。臨床試験への参加が、患者への負担を高め、試験参加を困難にするものになってしまっては本末転倒です。

myMedidataは、患者とともに、患者のために作られた単一の患者ポータルです。eCOA、同意、センサー、支払いをはじめとする患者のすべての活動を1つの連携したエクスペリエンスに集約し、試験の進展に合わせて一貫した参加を維持します。

Video transcript: Lisa has been an oncology patient for three years and takes an active role in her health care. Lisa recently joined the MyMedidata Registry to learn more about clinical trials so she can find a research study that may be a good fit for her. One day, Lisa receives a notification from MyMedidata about a study that may be of interest to her. Lisa shows her doctor the information about the trial she received from MyMedI Data. They discuss the trial and determine it could be a good fit, but realize the study research center is a two and a half hour drive away from Lisa's home. Lisa's doctor calls the primary investigator of the study, Doctor. Aliyah, to discuss the trial and determine if Lisa may be a good candidate for participation. Doctor. Aliyah and Lisa connect directly over a My Medidata Live Video Call to review the study information. Doctor. Aliyah explains the consent process to Lisa and asks her to watch the video and discuss the study opportunity with her loved ones. Lisa watches the video and decides she wants to participate and signs the eConsent form through her My Medidata account. Lisa also consents to link her electronic health record data, such as previous surgeries or other medical related information, to her clinical trial data through Medidata Link in order to allow researchers to learn more about her health and possibly remove the need for extra clinic visits. Doctor. Aliyah checks Lisa's electronic health record, EHR information, and transfers relevant data into RAVE EDC, the electronic data capture system. Lisa is now a participant in the study. Using a hybrid decentralized clinical trial model, she has some visits in the clinic and some at home with medication and other study supplies being shipped directly to her home. Out of the five site visits required in the study protocol, she is able to complete three at home. This flexibility significantly reduces Lisa's travel burden and saves her from needing to take several days off from her job. She wears a sensor to collect some data information and she enters some into a study diary application on her phone. During study visits on-site and through video visits, Aliyah and Casey, the study coordinator, enter information into Ray VDC. Her study doctor can also see her diary responses, as well as her sensor and image data, all in one place. It's easy for Doctor. Aliyah to see how Lisa is doing in the study. Once Lisa has completed her clinical trial, she transitions from the study into long term follow-up through My Medidata registries. She learns that the medication was approved and her participation helped many others. She also receives her clinical trial data back and is able to keep access to it on her MyMedidata account where she can share it with her primary care doctor. Lisa is happy with how much support she received through every step of her clinical trial journey. Because of this, she's even more interested in joining future clinical trials.

1つのアカウントで
試験参加をシンプルに

myMedidataは、患者の参加を単一の一貫したエクスペリエンスに集約します。1つのアカウントで、患者の負担を軽減し、実施施設の連携を簡素化し、試験全体を通しての継続参加をサポートします。

患者中心の 設計
デバイスに依存しない
境界のない治験

患者と医療機関の連携を維持

患者

すべての治験参加活動を1か所に集約

患者がすべての治験活動を行える場所を1つにまとめることで、余分なアプリ、ログイン、不要な手順をなくします。

myMedidataは、試験の全期間を通じて、参加とエンゲージメントの維持を容易にします。

Video transcript: Lisa has been an oncology patient for three years and takes an active role in her health care. Lisa recently joined the MyMedidata Registry to learn more about clinical trials so she can find a research study that may be a good fit for her. One day, Lisa receives a notification from MyMedidata about a study that may be of interest to her. Lisa shows her doctor the information about the trial she received from MyMedI Data. They discuss the trial and determine it could be a good fit, but realize the study research center is a two and a half hour drive away from Lisa's home. Lisa's doctor calls the primary investigator of the study, Doctor. Aliyah, to discuss the trial and determine if Lisa may be a good candidate for participation. Doctor. Aliyah and Lisa connect directly over a My Medidata Live Video Call to review the study information. Doctor. Aliyah explains the consent process to Lisa and asks her to watch the video and discuss the study opportunity with her loved ones. Lisa watches the video and decides she wants to participate and signs the eConsent form through her My Medidata account. Lisa also consents to link her electronic health record data, such as previous surgeries or other medical related information, to her clinical trial data through Medidata Link in order to allow researchers to learn more about her health and possibly remove the need for extra clinic visits. Doctor. Aliyah checks Lisa's electronic health record, EHR information, and transfers relevant data into RAVE EDC, the electronic data capture system. Lisa is now a participant in the study. Using a hybrid decentralized clinical trial model, she has some visits in the clinic and some at home with medication and other study supplies being shipped directly to her home. Out of the five site visits required in the study protocol, she is able to complete three at home. This flexibility significantly reduces Lisa's travel burden and saves her from needing to take several days off from her job. She wears a sensor to collect some data information and she enters some into a study diary application on her phone. During study visits on-site and through video visits, Aliyah and Casey, the study coordinator, enter information into Ray VDC. Her study doctor can also see her diary responses, as well as her sensor and image data, all in one place. It's easy for Doctor. Aliyah to see how Lisa is doing in the study. Once Lisa has completed her clinical trial, she transitions from the study into long term follow-up through My Medidata registries. She learns that the medication was approved and her participation helped many others. She also receives her clinical trial data back and is able to keep access to it on her MyMedidata account where she can share it with her primary care doctor. Lisa is happy with how much support she received through every step of her clinical trial journey. Because of this, she's even more interested in joining future clinical trials.
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myMedidataが提供する統合機能

myMedidataは、Medidataの患者向けソリューションを単一のエクスペリエンスに統合し、治験期間を通じて参加、コミュニケーション、データ収集の連携を維持します。
これにより、患者には一貫したエクスペリエンスが、治験チームには統一された患者データソースが提供されます。

注目のリソース


分散型臨床試験の価値

分散型およびハイブリッド型試験モデルが、患者の試験参加、医療機関のワークフロー、試験の実施にどのような変化をもたらしているか、また、その変化が今後の試験を計画するスポンサーにとって何を意味するのかについて、MedidataのCEOが語ります。

Video transcript: Welcome to the HBR Video Quick Take. I'm Todd Puzan, senior editor for Research and Special Projects at Harvard Business Review. Decentralized clinical trials, or DCTs, use a method of conducting clinical trials, where parts or all of the trial happen outside a traditional physical clinic or trial site. This opens up barriers to participation, enabling more patients to participate in research. And it enhances the overall trial experience for everyone. Anthony Costello is CEO of Patient Cloud at Dassault Systeme. In this role, he leads the development of Medidata's patient facing activities and solutions, including decentralized trials technology and strategy, Patient Cloud, Dassault Systeme product apps, My Medidata patient portal, disease registries and recruitment, telehealth and virtual visits, and Sensor Cloud and biomarker discovery. He's here today to talk to us about the rising adoption rates of DCTs and how these solutions affect research. Anthony, thank you for joining us. Thanks so much for having me, Todd. Anthony, what do decentralized trials and the use of new technology mean for patients, for pharmaceutical companies, for doctors? You know, we're in such an interesting time in the history of clinical trials and research. If you think about the way trials have been done traditionally, they're very heavily centralized, meaning patients travel to a research center often many times per month for months and months during a clinical trial. So what we mean when we say trials are now being decentralized is that the research is moving outside these central research sites and more into the patients' real lives. And the reason this is so important for the industry is if you think about the way research gets done and then new drugs get commercialized into the market, patients use these products in their real lives, in the real world, obviously not in a method that's centralized around a research center, but in their day to day lives. We're trying to move the industry and the research part of discovery into the real world where these drugs will actually be used after they're commercialized. It's a critical moment for the way research gets done, the pace of research, the ease of research for patients, the quality and quantity of data that we're capturing. All things that are much easier to get and to achieve in a decentralized model. Okay, so pharmaceutical companies, what do they need to be thinking about when they're considering a DCT model for research? This has been the real challenge for our industry. We have a conservative pharmaceutical industry, very largely based on regulation, paper processes, paper data capture, paper consent signatures, and so on. And a lot of what we've done over the last few years as an industry is we've begun to embrace and leverage the natural curves in the world of technology. Patients have more technology in their hands. They're more accustomed to using it. They're more trusting of providing information and receiving information through digital devices. Most patients carry some sort of device with them in their pocket all day, every day that's perfectly suitable for research. So the kind of hump to get over has been will pharma decide to use these capabilities in this kind of, call it this new digital era, as a way to conduct the research that maybe we formerly would have done in paper or a much more cumbersome process. So if you combine the idea that we want to decentralize outside of a site setting, Then you add in, we have the technology, the patients have the technology, they're comfortable with it, we can scale it, it's affordable. All of these things that you couldn't say ten years ago, or maybe even five years ago in some cases. You start to layer in things like wearable sensors that are getting easier to use, better battery lives, smarter, faster, better quality data. You kind of put it all together and we're in this perfect storm in the industry right now to hyper accelerate research across all different types of disease indications. We saw a little bit of this during COVID, maybe I'll call it kind of a foreshadowing of where our whole industry tries to go now. Because of a global pandemic, there was a lot of kind of consolidation around, let's do this faster, let's have more outreach to patients, let's decentralize. Now you're seeing that become the new normal, the trend, and everyone's looking for ways to leverage this perfect storm, if you will, as a way to change the way all clinical trials work into the future. And if we do it right, what we'll be doing is going from a world where we try to expose as few patients as possible to an experimental product, which obviously we always want to do that, but we want to expose the right patients, we want to do it in a way that's not too burdensome for them, and we want to make sure that when that drug gets approved and hits the market and millions of people take it, that we've done the research in as close a setting as we possibly can to the kind of real world commercial setting where those people will use that product. That sounds great. So a patient, how does a patient participate in a DCT? You know, interestingly, I would say patients don't get to choose DCTs as much as DCTs choose them. It's because if you're a patient, you enroll in a study, many times because you have no other healthcare option for your particular disease. Sadly, many patients, the clinical research may be the last option that they have after trying everything else for whatever condition they have. So a patient will choose a study out of necessity in a lot of cases, and hopefully what we're aspiring to support in this industry and what we're working with our customers to try to achieve is, more optionality for that patient on that study to be able to use these technologies in their real world setting. Patient burden is a huge problem in our industry. Sticking on these trials for a year, a year and a half, going back and forth to study centers all the time is very burdensome. We lose a lot of patients, and frankly we have a lot of patients who qualify for the study, they need the study, they have the right set of inclusion criteria for that study, but they simply can't participate due to geographical proximity to some study center that's running that trial. So decentralization, if you're a patient on a study that happens to be decentralized, you're much more likely to stay with that study throughout, to be able to participate in that study regardless of where you live, and then, as I said earlier, to be able to provide real world data from your day to day activities that are critical to the pharmaceutical company really understanding how their drug's gonna work when it hits markets. So it's a hard choice to make for our customers. It is a challenge to decentralize a clinical program that you have formerly run entirely at research centers, but if you do it, there's a huge upside both for patients and for the speed and accuracy of the research. We're expecting that both of those things are going to cause a forever new trend of decentralization in clinical trials. That's great. It sounds like a very promising set of developments. Anthony, thank you so much for being with us today. This is fascinating. Thanks again for having me. It's been fun, I appreciate it. To learn more about Medidata and decentralized clinical trials, please visit the link below.
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よくあるご質問

はい。myMedidataは、患者が治験に関する学習、同意、アンケートへの回答、支払いの処理など、すべての治験活動にアクセスできる単一のポータルとして設計されています。この統合されたアプローチにより、複数のログインやアプリケーションが不要になり、患者の体験が効率化されます。

はい。myMedidataはウェブでのアクセスに加え、iOSとAndroidの両方で利用可能なネイティブアプリがあり、「Bring Your Own Device」(BYOD)モデルと支給デバイスの両方をサポートしています。 

はい。myMedidata Registriesは、患者の参加を単発のものから、治験前後のエンゲージメントアプローチへと拡大します。これにより、スポンサーは患者に自社の試験について情報を提供し、エンゲージメントを高め、治験開始前に適格な参加候補者のプールを構築し、治験後には将来の治験機会をフォローアップすることができます。

患者はmyMedidataアカウントを通じて、同意、eCOA、センサー、支払い、遠隔医療など、治験タスクを完了するために必要なすべてのツールに、施設内またはリモートでアクセスできます。myMedidataを通じて収集されたすべてのデータはRaveに流れ込み、施設はリアルタイムで状況を可視化してコンプライアンスを確保できるとともに、患者の移動負担を軽減します。 

はい。Medidataは、クライアントとパートナー向けに、セルフペースとインストラクター主導の両コースを含む、さまざまなトレーニングオプションを提供しています。利用可能なコースの詳細やリソースへのアクセスについては、Medidata Global Education and Trainingのセクションをご覧ください。