H1 Blog

OCTOBER 16, 2023

Improved Success Rate: AI’s ability to analyze vast datasets can increase the likelihood of identifying successful drug candidates, thus reducing the number of costly failures in later-stage clinical trials. For more information on how to integrate AI into your workflow, request a demo.

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H1 Blog

JULY 30, 2024

Increasing diversity in clinical trials not only makes the findings more relevant to various patient groups, but also enhances knowledge about the disease or medical product being studied. This allows the trial to achieve more precise results at the indication level through leveraging comprehensive information from across the globe. “I

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H1 Blog

DECEMBER 11, 2024

In this edition, our CEO and co-founder, Ariel Katz, along with Regional VP of Trial Landscape, Ryan Brown, share their top predictions for 2025. Drug Policy There will be significant changes in clinical trials & drug development due to the Inflation Reduction Act.

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H1 Blog

JULY 5, 2023

The success of drug development and approval relies heavily on the ability to identify diverse patient populations for clinical trials. From trial site feasibility to successful trial recruitment, diversity within a trial population helps ensure the safety and efficacy of drugs that reach the market. African Americans).

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H1 Blog

JUNE 8, 2023

The drug development process is known to be often expensive, lengthy, and full of trial and error before finding success. To learn more about how H1 can empower medical affairs teams to diversity KOLs and HCPs leveraging H1’s HCP Universe , request a demo.

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Codon

MAY 22, 2023

Verve already started a Phase 1b trial in New Zealand last July. halted a Verve trial in the U.S. Read A chikungunya vaccine induced high levels of neutralizing antibodies in a phase II trial. Read CRISPR was not responsible for the death of 27-year-old Terry Horgan in a recent gene therapy trial for Duchenne muscular dystrophy.

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DNA Engineering Science Trials 57

Codon

MAY 22, 2023

Verve already started a Phase 1b trial in New Zealand last July. halted a Verve trial in the U.S. Read A chikungunya vaccine induced high levels of neutralizing antibodies in a phase II trial. Read CRISPR was not responsible for the death of 27-year-old Terry Horgan in a recent gene therapy trial for Duchenne muscular dystrophy.

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DNA Engineering Science Trials 52

Practical Cheminformatics

JANUARY 8, 2024

In November and December, several large pharmas held “AI Day” presentations featuring LLM applications for clinical trial data analysis. Aside from some very brief demos on code generation and literature searches, mentions of LLM applications in preclinical research were scarce.

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Codon

JUNE 26, 2023

A live demo is available online, but “it chews through OpenAI credits,” Patel says. There’s a live demo available online. “Right now, it can only make one protein at a time,” Gershon says, simply because the demo has limited compute resources. “Every query is like $2.” A Mycoplasma cell.

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DNA Therapies Engineering Clinical Trials 52

Codon

JUNE 26, 2023

A live demo is available online, but “it chews through OpenAI credits,” Patel says. There’s a live demo available online. “Right now, it can only make one protein at a time,” Gershon says, simply because the demo has limited compute resources. “Every query is like $2.” A Mycoplasma cell.

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DNA Therapies Engineering Clinical Trials 52

Codon

MAY 30, 2023

Read Engineered bacteria to accelerate wound healing: an adaptive, randomised, double-blind, placebo-controlled, first-in-human phase 1 trial. R21, developed at the University of Oxford, was up to 80% effective in a small clinical trial of 450 children in Burkina Faso. ‘OK’ to start clinical trials. Fierce Biotech.

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Codon

MAY 30, 2023

Read Engineered bacteria to accelerate wound healing: an adaptive, randomised, double-blind, placebo-controlled, first-in-human phase 1 trial. R21, developed at the University of Oxford, was up to 80% effective in a small clinical trial of 450 children in Burkina Faso. ‘OK’ to start clinical trials. Fierce Biotech.

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DNA RNA Engineering Vaccine 52

Agency IQ

MAY 31, 2024

Conference ( OPEN ) European Federation of Pharmaceutical Industries and Associations (EFPIA) 6/04/2024 6/05/2024 Third listen-and-learn focus group meeting of the Quality Innovation Group Webinar/Seminar ( OPEN ) EMA Quality Innovation Group (QIG) 6/05/2024 6/05/2024 Procurement Working Party Committee Meeting ( CLOSED ) British In Vitro Diagnostics (..)

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H1 Blog

DECEMBER 18, 2023

How will AI impact clinical trials? Solutions will also emerge that will make it easier to navigate available clinical trials—something like a ‘Zillow.com for trials’ that puts the patient experience at the center. Will FDA legislation improve diversity? What platforms will key opinion leaders adopt?

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Agency IQ

DECEMBER 1, 2023

Comment periods for EMA documents (such as concept, reflection, and guidance papers) generally stay open for at least six months, though these timelines can vary drastically. policy, such as public registers, drafts, reflection papers, concept papers, and guidance documents expected into Q1 2024.

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H1 Blog

NOVEMBER 29, 2023

Breaking the Barriers: How Inaccurate Trial Records Are Delaying Drug Development and Limiting Diverse Patient Populations In an October 2023 report , BMC Medicine completed a follow-up on a 10-year effort to understand, report on and track data sharing challenges with big pharma, specifically for clinical trials.

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Advarra

DECEMBER 12, 2024

a clinical trial management system [CTMS], HR systems, learning management systems [LMS]) are stakeholders using? Demo requests: Schedule demonstrations with each potential vendor for a more hands-on experience. This will help in identifying must-have features and potential pitfalls. For example, what other systems (e.g.,

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