Drug Discovery World

MARCH 2, 2023

” The role of AI in rare disease clinical trials might hold the key to helping the UK achieve this vision. AI is revolutionising clinical trials and drug developments just as it is transforming other sectors, but in order for AI to make progress in rare diseases, the UK needs further investment to increase uptake and use.

Development 52

Development Drugs Clinical Trials Clinical Trials 52

Roots Analysis

JANUARY 22, 2024

This resulted in the discovery of an individualized concept of treatment known as oncology precision medicine which primarily utilizes the patient’s genomic information to provide gene-targeted diagnostics and therapeutics. Data Handling: Genomic data essential for the implementation of precision medicine is highly sensitive and personal.

Medicine 40

Medicine Genetics Genome Genomics 40

Camargo

NOVEMBER 11, 2020

In November 2017, Foundation Medicine received approval for FoundationOne CDx , a genomic profiling test for solid state tumors, which paved the way for partnerships with pharma companies’ therapeutics. Manager of Regulatory Compliance. In 2019, Foundation Medicine and Bayer Healthcare Pharmaceuticals, Inc. Co-Authors: Jenny Fielder.

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Development Bioequivalency Generic Drugs Production 242

XTalks

MAY 23, 2024

XTALKS WEBINAR: Enhancing Efficiency in Early-Phase Oncology Trials: Strategies for Accelerating Data Flow Live and On-Demand: June 24, 2024, at 11am EDT (4pm BST/UK) Register for this webinar today to gain insights into how you can navigate and overcome data flow challenges in early-phase oncology clinical trials.

Life Science 72

Life Science Dermatology Drug Delivery Systems Medicine 72

XTalks

FEBRUARY 4, 2021

The power of leveraging clinical data to decipher disease mechanisms and fuel drug discovery has rapidly grown in the era of genomics and personalized medicine. Genuity Science focuses on population genomics as a tool to derive novel biological insights through partnerships with industry-leading pharmaceutical and biotech companies.

Research 98

Research Biobanking Drugs Genome 98

Advarra

NOVEMBER 29, 2022

The first is titled, Human Gene Therapy Products Incorporating Human Genome Editing , and provides recommendations on the information to include in IND filings for these therapies, including study design, safety, and manufacturing. Lack of agreement on surrogate endpoints in clinical trials was another key theme during the session.

Gene Therapy 52

Gene Therapy Gene Production Clinical Trials 52

Drug Discovery World

DECEMBER 8, 2023

With human clinical trials with AI-designed drugs now ongoing, it’s only a matter of time until the FDA approves its first AI-designed drug. Combining these task-specific datasets with the knowledge acquired from custom-made LLMs enables us to model several biological phenomena with unprecedented accuracy.

Gene Therapy 64

Gene Therapy Gene In-Vitro Development 64

The Pharma Data

NOVEMBER 15, 2020

a publicly traded biopharmaceutical company, from 2012 to December 2019, managing its international, legal, quality, intellectual property and compliance functions, after serving in other executive roles at Acorda starting in 2004. She currently serves as a non-executive director on the board of Genfit, S.A., Before joining Acorda, Ms.

Clinical Trials 40

Clinical Trials Clinical Trials Production Trials 40

pharmaphorum

MAY 18, 2022

Genomics has unlocked entirely new insights to what exactly may cause certain neurological conditions. A lot more research is needed including large-scale clinical trials, which comes at a certain amount of investment and risk.”. The value of external science and strategic collaboration.

Gene Therapy 69

Gene Therapy Gene Genetics Development 69

The Pharma Data

NOVEMBER 17, 2021

The companies will work GSK’s moxie in functional genomics and combine their capabilities in CRISPR webbing and artificial intelligence to identifyanti-coronavirus composites that target cellular host genes. They will also apply their concerted moxie to probe SARS-CoV-2 and other coronavirus vaccines.

Antibody 52

Antibody In-Vitro Vaccination Vaccine 52

Advarra

SEPTEMBER 29, 2022

ClinicalTrial.gov information: Applicable for Phase 2 and later studies, must be verbatim as follows: A description of this clinical trial will be available on [link] as required by U.S. This Web site will not include information that can identify you. At most, the Web site will include a summary of the results.

Regulation 52

Regulation Research Genetics Compliance 52

The Pharma Data

NOVEMBER 24, 2020

The Notice of Compliance was granted under priority review and marks the first Health Canada approval of a PARP inhibitor in prostate cancer. Based on the available clinical trial data, a causal association between Lynparza treatment and VTE including pulmonary embolism has not been established. 72,1 (2017): 34-42.

Gene 52

Gene Hormones DNA Medicine 52

The Pharma Data

MAY 7, 2021

The EMA will evaluate all data on sotrovimab, including evidence from clinical trials, as they become available. The EMA will assess the medicine’s compliance with the usual standards for efficacy, safety and quality. They will also apply their combined expertise to research SARS-CoV-2 and other coronavirus vaccines.

Antibody 52

Antibody Trials Vaccination Vaccine 52

The Pharma Data

AUGUST 6, 2020

FDA for the first-line treatment of adult patients with metastatic or recurrent non-small cell lung cancer (NSCLC) with no EGFR or ALK genomic tumor aberrations. All clinical trial activities are planned to resume by the end of the year where local country restrictions have been lifted. In May, the company announced the U.S.

Production 52

Production Branding Marketing Licensing 52