TUCSON, AZ, NEW YORK, NY, and AUSTIN, TX – September 11, 2017 – Critical Path Institute (C-Path), CHDI Foundation, Inc. (CHDI), and The Clinical Data Interchange Standards Consortium (CDISC) announce the availability of a draft Huntington’s disease (HD) Therapeutic Area User Guide (TAUG-HD v1.0) for public review. The TAUG-HD v1.0 describes how HD clinical data should be recorded in a standardized database to establish common best practices across the healthcare industry for the recording, reporting, and sharing of clinically relevant disease-specific metadata, research data, and patient information. Use of the standard will allow the HD research community to compare and contrast data from different studies more easily and with more scientific rigor, and will make it easier for researchers to understand natural history, biomarker, and trial data in the future. It will also facilitate regulatory submissions for novel therapeutics.
Researchers and clinicians are encouraged to review TAUG-HD v1.0 and offer feedback. This input will be essential to ensure that neutral, consensus-based data standards are developed and adopted by a diverse global community that is committed to improving research processes and quality for the benefit of all.
The public review period begins on September 11, 2017, and extends through November 10, 2017. On September 12, CDISC will host a public webinar detailing the public review process; this webinar will be available online throughout the review period.
Huntington’s disease is a genetic, progressive neurodegenerative disease that causes a range of physical, mental, and emotional disabilities, including involuntary movements, cognitive decline, and behavioral changes. The disease is caused by an expansion mutation in the CAG repeat region of the huntingtingene, resulting in a toxic protein that leads to neurodegeneration. Around one person in 10,000 carries the mutated huntingtin gene, and each child of a parent with the mutation has a 50% chance of inheriting the disease. Current HD therapies only manage the severity of a subset of symptoms; there are no approved treatments to slow the disease’s progression.
“Huntington’s research is moving forward rapidly, with greater industry focus seeking to develop novel therapies,” said Martha Brumfield, PhD, C-Path President and CEO. “As we move forward with the aggregation of clinical data sets, it is our hope to create tools that will inform innovative clinical trial designs, which can help expedite development programs. It is an ideal moment for the development of a CDISC TAUG that will standardize nomenclature, formats, collection, and reporting of these new forms of data. C-Path’s collaboration with CHDI and CDISC on this user guide is both valuable and timely.”
“The HD research field is now at the threshold of important clinical developments that will help us move some of the promising therapeutic candidates in the pipeline to clinical trial,” said Cristina Sampaio, MD, PhD, Chief Clinical Officer at CHDI Management, Inc. “This collaboration to develop universal data standards is another example of how the highly collaborative nature of the HD research community can accelerate therapeutic development for the benefit of patients and their families.”
To review the therapeutic area user guide, please visit: https://www.cdisc.org/public-review/huntingtons-disease-therapeutic-area-user-guide-v10-available-public-review
TAUG-HD v1.0 describes the biomedical concepts relevant to HD clinical studies and the necessary metadata to represent such data consistently, allowing datasets from multiple sources to be compared or combined for analysis. TAUG-HD v1.0 focuses on the representation of data using the CDISC Study Data Tabulation Model (SDTM). Types of data covered include family history, genetics, and biomarkers to assess disease onset and progression. Specific biomarkers included in this user guide include neuroimaging assessments (MRI and PET) and biofluid biomarkers, with a focus on cerebrospinal fluid analytes.
TAUG-HD v1.0 was developed through the Coalition for Accelerating Standards and Therapies (CFAST) consortium, with clinical advice and input from CHDI, C-Path, CDISC, and other knowledge domain experts. CFAST, a joint initiative of CDISC and C-Path, was formed to accelerate clinical research and medical product development by creating and maintaining data standards, tools, and methods for conducting research in therapeutic areas important to public health, with invaluable support and advice from such organizations as the National Cancer Institute, Innovative Medicines Initiative, TransCelerate, and regulatory agencies including the FDA, Japan’s Pharmaceutical and Medical Devices Agency, and the European Medicines Agency.
CDISC standards have been adopted and used in more than 90 countries, and are required by regulatory authorities in the U.S. and Japan. To date, therapeutic area standards have been developed for more than 30 different disease areas, with most being developed under the CFAST program. Use of these standards from the start of clinical research programs has proven capable of saving both time and resources. HD researchers are encouraged to implement these standards into their processes.
Ann P. White
Source: CHDI Foundation