Medidataエクスペリエンス

単なる戦略を超えて
実行可能な唯一の
オペレーティングモデル

臨床試験は構造的な転換点を迎えています。プロトコルはより複雑化し、データ量は爆発的に増加しています。しかし、多くの組織では、照合チームによってつなぎ合わされた、分断されたシステムで業務を行っているのが現状です。

患者、データ、試験にわたるエクスペリエンスをつなぐことは、現代の臨床研究を大規模に維持できる唯一のオペレーティングモデルです。

Video transcript: The life sciences industry is shifting towards holistic solutions to not just extend lives, but improve them. Modern trials demand doing more with less. You need a trusted partner that solves complexities while achieving better, faster outcomes through technology, AI, and expertise. That's why we designed the metadata experiences. These patient, data, and study experiences unite for peak speed, efficiency and decisive action. So you can unleash clinical data's might, ignite insights and forge lasting trust and participation in your trials. All this powered by Metadata's unified platform with AI driven intelligence informed by over thirty six thousand studies. Don't just run trials, revolutionize them. The future of clinical research is here and it's built on experience. Are you in?

1つのオペレーティングシステムとしての
エクスペリエンス

治験依頼者やCROが求めているのは、これ以上のポイントソリューションではありません。彼らが求めているのは、エンドツーエンドのワークフロー、ベンダーの複雑性の軽減、統合ポイントの削減、そして測定可能な迅速化です。

エクスペリエンスをつなぐことは、データ、ワークフロー、意思決定がリアルタイムで相互に情報を提供し、強化し合う、継続的でインテリジェントに統合されたシステムを構築することで、試験全体を強化します。

実績のあるグローバルプラットフォーム

80 %

2025年のFDAによる全新規医薬品承認のうち

世界中で信頼

2.3 K+

140カ国以上の顧客および治験実施施設

トレーニング済みの組み込みAI

70 B+

年間データポイント

数十年にわたる
縦断的データ

38 K+

の臨床試験でMedidataのテクノロジーが使用されています

Patient Experience

臨床試験のROIを高めるエンゲージメント

臨床試験中および試験後を通じて、被験者募集の強化、登録の迅速化、エンゲージメントの深化、アドヒアランスの向上、リテンションの維持を促進します。

臨床試験の負担を軽減し、ワークフローを効率化する統合プラットフォームで、患者と実施医療機関を支援します。

Patient Experienceの詳細

Data Experience

学習するデータ。行動するAI。

臨床試験のライフサイクル全体でデータは劇的に増加します。
データを設計、統制、活用し、常にその完全性、可視性を確保してインサイトを引き出します。

試験構築からデータベースロックまで、インテリジェントな自動化によってデータワークフローを簡素化し、データ品質を向上させます。

Data Experienceの詳細

Study Experience

結果を予測。パフォーマンスを加速。

完全な可視性をもって、設計から実行へ。



予測分析と組み込みAIを活用してリスクを予測し、早期に対処することで、臨床試験の計画と実施を加速します。

Study Experienceの詳細

注目のリソース


コードを超えて:臨床試験エクスペリエンスの変革

BBC StoryWorks制作のシリーズでは、MedidataのリーダーたちがAIと機械学習がどのように臨床試験を変革しているかを探求します。

Video transcript: I always knew I wanna be an astronaut when I was growing up. So these are just some of the kids' models that I've had for I don't even know how many years. And you've got space shuttle. This is everybody's dream. I got into college and really started pursuing my dream of becoming an astronaut. But unfortunately, in my sophomore year, got very sick and was diagnosed with Hodgkin's lymphoma. It took me a while to really wrap my mind around how significant my life was about to change. You know, when I got to college, I was so focused. I wanted to be an aerospace engineer. I wanted to go to space. Cancer really took that away from me. I just going through what I had to go through took a toll. So after graduation, I actually started my career in information systems. Ten years, into my career, I was diagnosed with breast cancer. It was a direct result of all the radiation I had is for my treatment with Hodgkin's disease. I was stunned to see that there had really been no change in the patient experience from when I was first diagnosed in nineteen ninety with Hodgkin's lymphoma and decided to step into helping health care improve the patient experience. The patient experience is critical in thinking about how you design studies and how clinical trials are ultimately executed. Clinical trial participation can be very tough on patients. It's incumbent upon all of us to put a focus on patients and the value that they bring to the research community and to take care of them as best as we can in the context of these studies. Our focus here is to lower the bar of participation by making it easier for them to capture data from home and minimizing the amount of time and effort it takes them to be able to participate in a study. So myMedidata is an app that patients use at home to provide their own information on how they're doing on the clinical trial. It helps reduce burden because patients give us the information that they have at home on a daily basis instead of waiting until they visit their doctor. And it also helps improve the fidelity of the data we get because we're getting it in real time. Yeah. And that and the the data life for a patient doesn't just start when the clinical trial starts. Oh, gosh. You've got all sorts of data before. When you take time to incorporate the patient perspective in clinical trial design, you pick up the nuance. You understand better how a patient's gonna move through that clinical trial experience. We've amassed a really valuable data set. Our view of the future of clinical research is that we find better ways to harness these data very quickly and then to layer on the power of AI so that we can accelerate the process of finding new therapies as fast as possible. So for this single simulant, the data are abstracted from potentially multiple patients. So simulants is part of our AI program. And the whole idea behind simulants is that we take this very large dataset that we have of of historical clinical trials data and we mix and match the information from lots of different patients to create simulated new patients that are actually AI constructs, but which are so close to the actual real patient that we can use those simulations as part of the research effort moving forward. AI. In some cases, we're able today to replace entire arms of clinical research studies, and we call this program synthetic control arms. Because we can take a patient who otherwise would have been brought onto a trial just to receive a standard of care or a placebo dose, and we can replace that patient with a synthetic control patient so that the real person doesn't have to be exposed to the placebo. We have highly sophisticated data, so privacy protection and abstracting away from the identifying information and those data are absolutely critical to what we do in our AI program. The clinical trial process is evolving at an enormous rate. There's an explosion of data availability being created in the world, and our long term goal as a company is to build full, what we call virtual twin models, where a person can have a perfect data twin. We bring a huge benefit to patients because the more we can use their virtual twin or programs like simulants, the more we can replace the kind of exposure that patients ultimately have to have on the trial. The reality is people are always gonna be dealing with illness or disease, but we're using the technology that's available to us today to make that experience better for the people that are dealing with these illnesses. I've accepted that I'm never going to the moon, but I have to say back here on Earth, I like to think that what we're doing at Medidata is really out of this world.
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よくあるご質問

Medidata Experiencesは、単一のインテリジェントなプラットフォーム上で患者、データ、試験のワークフローを統合し、臨床試験のライフサイクル全体にわたって人、プロセス、システムをつなぎます。

AIはワークフロー全体に組み込まれており、リスクを検出し、データ品質を向上させ、定型業務を自動化し、実用的なインサイトをリアルタイムで提供します。

治験依頼者やCROが求めているのは、これ以上のポイントソリューションではありません。彼らが求めているのは、エンドツーエンドのワークフロー、ベンダーの複雑性の軽減、統合ポイントの削減、そして測定可能な迅速化です。 



当社のExperiencesをつなげることで、議論の焦点はソフトウェアの調達から業務変革へと移行します。規模、データの深さ、規制における信頼性、そして組み込まれたインテリジェンスを兼ね備えたパートナーをご活用ください。