Fierce BioTech

JULY 28, 2023

State of Clinical Inventory and Sample Management for Clinical Trials This report summarizes the survey findings from biopharma professionals on the impacts of inefficient, manual processes for managing clinical supply and samples on budgets, timelines, data integrity, and patients — and the need for change. Download here!

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PPD

MARCH 21, 2024

When participating in clinical trials, pediatric populations require distinct considerations for their safety and well-being — which can present unique challenges for drug developers. Five Strategies to Tailor Your Pediatric Clinical Trials to the Child’s Needs 1.

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The Pharma Data

NOVEMBER 26, 2020

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you agree to having your details passed onto the sponsor who may promote similar products and services related to your area of interest subject to their privacy policy. Download Your Copy. . Download Your Copy.

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Fierce BioTech

MAY 30, 2024

Quantify Cancer With Methylation-Based ctDNA Detection Download this resource to accelerate your oncology clinical trials, optimize patient enrollment, and monitor minimal residual disease and molecular response effectively.

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Crucial Data Solutions

MAY 31, 2023

Clinical trials continue to move closer to patients. Many patients, now, can participate fully in clinical trials largely from home by utilizing remote data collection technologies such as ePRO, eConsent, virtual visits, and more. They do so, largely, from mobile devices – often their very own smartphones.

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PPD

NOVEMBER 4, 2024

This year’s findings reveal a nuanced landscape where rising clinical trial costs, complex protocol designs and patient recruitment issues have emerged as significant challenges. Patient recruitment was revealed as the second biggest challenge facing drug developers in 2024, unseated by the rising cost of clinical trials.

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Fierce BioTech

MAY 31, 2024

Generative AI: Powering the next era of life sciences innovations Download this eBook to explore how generative AI is revolutionizing life sciences. Learn to accelerate drug discovery through AI-powered protein folding, enhance clinical trials with data analysis, and optimize manufacturing with real-time AI monitoring.

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Agency IQ

AUGUST 23, 2024

EMA issues more updates to prepare for clinical trials transition Offices throughout the EU—including those of the EMA—have slowed operations for the summer holiday, but that didn’t keep the EMA from publishing a stack of updated documents. Per the CTR, all clinical trials are to be moved over to the CTIS by January 30, 2025.

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Fierce BioTech

NOVEMBER 7, 2024

Download Now. Guardant Health liquid biopsy clinical trial biopsy Resource Type Whitepaper Guardant Logo Thu, 11/07/2024 - 11:09 Clinical Data Biotech Clinical Data Research Landing Page Url [link] Byline Sponsored by: Guardant Health

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Predictive Oncology

AUGUST 8, 2024

A recent white paper released by Predictive Oncology’s highlights the challenge of late-stage clinical trial failures and the company’s ability to better navigate those obstacles and increase the probability of technical success which is a key metric in target selection, clinical trial design and pipeline replenishment.

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Perficient: Drug Development

AUGUST 2, 2023

For learning purposes, you can request a trial license as well. Purchase/Trial Sitecore TDS and SVS license Step 01: Goto the TDS site Step 02: Click on the Free Trial link Step 03: Click the Try TDS button Step 04: Submit the TDS free trial form. Step 05: After submission, you need to download a package and install it.

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Conversations in Drug Development Trends

SEPTEMBER 20, 2023

Download our poster today. The post Bioanalysis through automation: Our top four takeaways appeared first on Worldwide Clinical Trials. Time Savings: With the increased quality and throughput, we can validate assays in just a few days as opposed to weeks.   Want to learn exactly how we did it?

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Fierce BioTech

JANUARY 26, 2024

Blueprint for Modern Patient Recruitment Every day, a clinical trial is delayed due to recruitment planning issues. Discover how leading sponsors are redefining the approach to patient recruitment in clinical trials. Download now. Download now.

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PPD

OCTOBER 31, 2024

From adapting to complex new trial designs to embracing cutting-edge technologies, staying ahead requires a deep understanding of the current landscape. Drug development The rising cost of clinical trials is the top challenge this year, due to increasingly complex protocol designs and difficult patient recruitment.

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The Pharma Data

AUGUST 7, 2020

The governing body claims this proposal could have positive effects on mitigating burdensome requirements for gene therapy clinical trials in the future. In this light, Pharma IQ’s weekly round-up focuses on advancing therapies and clinical trials to combat Covid-19. Dr. Francis S.

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Alta Sciences

JANUARY 24, 2024

Discover the Power of Driving Simulations for CNS Side-Effect Analysis blussier Wed, 01/24/2024 - 18:25 HTML Start Your Driving Trial Quickly—Simulators On-Site Driving simulator studies are a safe, efficient, and effective alternative to on-the-road driving trials for CNS-active drugs. jpg Tags Clinical Trials Weight 1

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Agency IQ

AUGUST 1, 2024

You will receive an email with access to download at the start of RAPS Convergence 2024. To access additional insights from our experts, sign up for our free newsletter, FDA Today , attend one of our monthly webinars , and explore all of AgencyIQ’s subscriber features through a free trial.

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The Pharma Data

JANUARY 20, 2021

21, 2021 /PRNewswire/ — Calliditas Therapeutics AB (publ) (“Calliditas”) (Nasdaq OMX: CALTX) (NASDAQ: CALT) today announced that all 360 patients have been enrolled for the global Phase 3 clinical trial NefIgArd, which investigates the effect of Nefecon® versus placebo in patients with primary IgA nephropathy (IgAN).

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Fierce BioTech

AUGUST 1, 2023

Support for the next generation of clinical and IVD trials requires a unique, multi-specialty approach. Download here! Support for the next generation of clinical and IVD trials requires a unique, multi-specialty approach. However, these modalities add significant complexity to pharma and biotech research projects.

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DrugBank

OCTOBER 30, 2024

From advancing drug discovery, managing clinical trials, or developing new healthcare solutions, reliable and flexible access to quality data is essential for success. Instead of traditional CSV downloads, users receive direct access to a fully queryable, ready-to-use database within the Snowflake ecosystem.

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The Pharma Data

OCTOBER 19, 2020

We remain committed to further progressing our trial preparations, as we look forward to initiating a U.S. Phase 2 trial for Berubicin during the first quarter of 2021.” In addition to its manufacturing efforts, the Company has also made progress in its clinical trial preparations. .

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Agency IQ

MAY 8, 2024

You will receive an email with access to download at the start of the DIA 2024 Global Annual Meeting. To access additional insights from our experts, sign up for our free newsletter, FDA Today , attend one of our monthly webinars , and explore all of AgencyIQ’s subscriber features through a free trial.

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Perficient: Drug Development

SEPTEMBER 18, 2024

Getting Started: Prerequisites and Setup Before diving into the setup process, ensure you have: Splunk Cloud Account: An active account (free trial or paid subscription). Universal Forwarder Installation Package: Downloaded for your specific operating system. Access to Log Files: Identified and accessible log files for monitoring.

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Predictive Oncology

JUNE 27, 2023

Download Report Schedule a meeting With the high rate of clinical trial failures, how can we incorporate tumor heterogeneity earlier in the process? Can it really be achieved prior to clinical trials…even in the early drug discovery phase?

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Agency IQ

JUNE 28, 2024

New guidance provides definition for orphan device, offers alternative trial designs New guidance from the European Commission outlines alternatives for full pre-market clinical trials for orphan devices, defined by the Commission for the first time. The guidance notes that all approaches should be justified.

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PPD

NOVEMBER 30, 2023

These shifts are a prelude to further change and progress in the clinical trial landscape in 2024. Overall, new technological approaches applied in these settings show remarkable potential to make trials more robust, promote more reliable data acquisition and keep trials on-time and on-budget. This year, the U.S.

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Agency IQ

FEBRUARY 29, 2024

Thank you for signing up to receive the PFAS Explainer You will receive an email with access to download at the start of the GlobalChem Conference. Be sure to visit us at booth #103 during the conference.

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Conversations in Drug Development Trends

MARCH 7, 2024

When conducting first-in-human (FIH) clinical trials, small to midsize pharmaceutical and biotechnology companies are faced with several crucial choices that can shape the trajectory of their drug development pathway. For additional insights, download our full white paper, “ First-in-Human Studies: IND or CTA? ”.

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Conversations in Drug Development Trends

JUNE 13, 2024

Pharmacogenomics (PGx), the study of how genes affect a person’s response to drugs, has brought significant changes to the clinical trial industry. Download our full poster to explore the comprehensive analysis and our findings and to discover how DNA sample collection can impact the effectiveness of personalized medicine.

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The Pharma Data

JANUARY 12, 2021

a biopharmaceutical company focused on the development of first-in-class therapeutics for the treatment of cancer, today announced the completion of the Phase 1b clinical trial conducted by the NCI with its lead clinical candidate zotiraciclib (ZTR/TG02), a potent oral cyclin-dependent kinase 9 (CDK9) inhibitor. .

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The Pharma Data

DECEMBER 8, 2020

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you agree to having your details passed onto the sponsor who may promote similar products and services related to your area of interest subject to their privacy policy. . Download Your Copy. . Download Your Copy.

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The Pharma Data

DECEMBER 20, 2020

Followed by Russia , Indonesia, and Korea, the second phase of the COVID-19 clinical trial was approved in Italy on Friday, December 18, 2020. Currently, it is smoothly progressing with the approval for Phase 2 clinical trials in four countries, and it is expected to see the results sequentially starting as early as the third quarter of 2021.

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The Pharma Data

JANUARY 17, 2021

The results provide an opportunity for the company to pursue a pivotal Phase 2/3 clinical trial in patients with primary biliary cholangitis (PBC), based on interactions with the FDA. The trial consisted of a single ascending dose (SAD) part and a multiple ascending dose (MAD) part with dosing up to 1600mg/day.

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The Pharma Data

OCTOBER 16, 2020

As pharma companies search for solutions to avoid cancelling or delaying clinical trials, virtualizing trials are fast becoming commonplace during the Covid-19 pandemic. With many nationwide and regional lockdowns coming into force, virtual clinical trials are proving to be an effective way to monitor patients remotely.

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Predictive Oncology

JUNE 28, 2023

Schedule a meeting Download case studies Optimize your formulation development challenges for biologics without disrupting your workflow.

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Perficient: Drug Development

JANUARY 11, 2024

Creating Groovy script to download ERP Actual file and loading to Consolidation tool. year=<FISCAL_YEAR>&month=<PERIOD>” The JSON response “jsonResponse1” will contain details of the trial balance files that have been generated in the SFTP location. Please follow the steps below to do so.

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The Pharma Data

DECEMBER 14, 2020

The Phase II SBIR grant is a follow-on 2–year award that will support testing of Alume’s fluorescent nerve targeting agent in an ongoing Phase 1/2 clinical trial in patients undergoing Head and Neck Surgery. View original content to download multimedia: [link]. About Alume Biosciences, Inc. SOURCE Alume Biosciences.

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