Gathers clinical trials about amyotrophic lateral sclerosis (ALS). PRO-ACT is a public database which compiles datasets from industry and academic clinical trials according to a comprehensive common data structure with the aim of easing research about ALS. It includes more than 10700 demographics data and over 68000 longitudinal information on revised ALS Functional Rating Scale (ALSFRS(-R). Information about vital capacity, vital signs, safety labs, concomitant medications and adverse events are also provided.
Works on making clinical trial data from the FDA (US Food and Drug Administration) more easily accessible and searchable. OpenTrialsFDA extracts the relevant data from the FDA documents, link it to other clinical trial data and present it through this new user-friendly web interface. Through the OpenTrialsFDA interface, users are able to explore and discover the FDA data. In addition, the information has been integrated into the OpenTrials database, so that the FDA report can be linked to reports from other sources, such as ClinicalTrials.gov, EU CTR, HRA, WHO ICTRP, and PubMed.
Shares human subjects data from all clinical trials funded by the National Institute of Mental Health. NDCT was created by the NIMH, it supports additional mental health-related clinical trial communities by accepting and sharing this data regardless of funding source. Qualified researchers can request access to shared data, as well as the other repositories that make up the NIMH Data Archive. The user can view summary-level data, or can request access to query and download subject-level data.
Proposes a data retrieval platform. D360 includes functions for data filtering, exploration and visualization. This program permits users to create project dashboards and to formulate complex queries without important specifications about data localization. It also incorporates tools and supports for virtual compounds as well as features for real and conceptual compound prioritization.
Allows users to upload, validate and match pre-clinical study data for desired terminology. PCSS is a program made for study managers, toxicologists, pathologists, and data scientists. It can capture and query file-based pre-clinical study data based upon the CDISC SEND standards. It can also serve for mapping alternate names for scientifically equivalent tests to preferred terms using a terminology tool.
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