Drug Discovery World

JANUARY 24, 2023

Virtual clinical trials ‘Virtual’ and ‘technology’ are concepts which are readily exchanged in this industry, but these are more than just buzzwords. The overall virtual clinical trials market is currently valued at $7.8 billion, with a projected growth of 14% per annum 1. We’ve shown that this type of model can work.

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pharmaphorum

AUGUST 9, 2022

The software is combined with traditional MRI scanning to improve the “accuracy and speed” of prostate cancer diagnosis by improving the diagnostic resolution of images, according to the company, which makes it available as a software-as-a-service (SaaS) to radiology departments.

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Advarra

APRIL 30, 2024

Maintaining complete and compliant documentation while managing the complex processes and interactions of clinical trial conduct is complicated. Investigator Site Files The ISF contains essential documents permitting evaluation of a clinical trial’s conduct. Remember, some staff may not need protocol-specific training.

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Pharmaceutical Technology

NOVEMBER 30, 2022

Development of vaccines to Phase I trials under the five-year $59m prototype project comprises additional $28.4m Additionally, the funds are intended to advance the vaccines to successful conclusion of Phase I clinical trials. in milestone payments.

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XTalks

MARCH 27, 2023

The first line of treatment for invasive candidiasis is a subset of antifungal medications called echinocandins, which includes caspofungin (brand name Cancidas), the drug that rezafungin was compared with in clinical trials. Once the fungus cannot synthesize β-(1, 3)-D-glucan, it undergoes osmotic instability and cell death.

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The Pharma Data

FEBRUARY 21, 2022

Our leadership in cardiology, radiology and women’s health is recognized worldwide, and we are expanding our presence in oncology, working tirelessly to bring forward new approaches that can change the treatment paradigm for patients,” said Stefan Oelrich, Member of the Board of Management, Bayer AG and President of Bayer’s Pharmaceuticals Division.

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Drug Discovery World

NOVEMBER 29, 2023

These findings closely matched the results of the corresponding real-life clinical trials. The researchers expect their model will be ready for use in a clinical setting within five years.

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WCG Clinical

MARCH 17, 2023

With many clinical research sites facing study start-up delays and backlogs, performing a coverage analysis efficiently and thoroughly is critical to the study start-up process. But why is the coverage analysis process so vital for clinical trials and how can research sites do it more effectively?

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pharmaphorum

JANUARY 24, 2022

Francisco Partners is picking up a range of databases and analytics tools – including Health Insights, MarketScan, Clinical Development, Social Programme Management, Micromedex and other imaging and radiology tools – for an undisclosed sum estimated to be in the region of $1 billion.

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Cloudbyz

APRIL 4, 2023

Source documents and case report forms (CRFs) are two types of documents that are commonly used in clinical trials to collect clinical data. However, the manual extraction of relevant clinical data from these documents can be time-consuming and error-prone.

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Scienmag

FEBRUARY 16, 2021

Food and Drug Administration (FDA)’s Center for Devices and Radiological Health (CDRH) will participate in this “collaborative community” A medical “collaboratory” is a forum in which multidisciplinary private and public sector members work together on medical […].

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XTalks

NOVEMBER 29, 2022

The study results will be presented at the Radiological Society of North America annual meeting , which is currently being held in Chicago, IL until December 1, 2022. XTALKS WEBINAR: Getting Neuroimaging Right — How to Succeed in Neurodegenerative Clinical Trials. What is ADHD and How is it Diagnosed?

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Scienmag

SEPTEMBER 18, 2020

ARRS promises to deliver the same clinically relevant experience for which its Annual Meeting has long been heralded: world-class educational activities led by the field’s foremost experts that span every subspecialty of radiology Leesburg, VA, September 18, 2020–The American Roentgen Ray Society (ARRS) will convene its 2021 Annual Meeting (..)

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Drug Discovery World

OCTOBER 24, 2022

The researchers say their next step is large animal trials and if successful, they look toward a Phase I clinical trial in humans. . “That makes us think that this approach might actually work better than external beam therapy for many other cancers, too.” .

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The Pharma Data

DECEMBER 23, 2020

Additionally, Phase 1 clinical data found INO-4800 to have a favorable safety and tolerability profile with no serious adverse events reported; only six Grade 1 adverse events (AEs) were observed, primarily minor injection site reactions. ” Findings from the Phase 1 Clinical Trial. mg and 2.0

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Bioengineer

JULY 15, 2021

“In clinical trials, we tend to go with the maximum tolerable dose, the idea being that radiation kills the cancer and the more we give, the better. professor of radiology at the University of Wisconsin School of Medicine and Public Health, in collaboration with co-author Reinier Hernandez, Ph.D., ” ###.

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pharmaphorum

SEPTEMBER 30, 2022

First and most obviously is the detailed data from the Clarity AD study reported this week, which will be revealed at the Clinical Trials on Alzheimer’s Congress (CTAD) in November. There will still be much debate about the exact license granted to the drug and cost-effectiveness deliberations, according to Prof Passmore.

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Triage Cancer

OCTOBER 15, 2020

In some cases, participating in a clinical trial may or may not be covered by a pharmaceutical company. It is important to bring actual disc images of any CT, PET or MRI scans that you have had as well as their corresponding radiology reports to your appointment. Clinical Trial Participation.

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The Pharma Data

JANUARY 27, 2021

The good news is that, more recently, “our ongoing surveillance and research suggests that there has been a rebound in [cancer] trial launches,” Lamont said. “This study speaks to a big decline in the launch of new trials during the pandemic,” Schilsky noted. “Some trials never resumed and may never.

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The Pharma Data

APRIL 17, 2021

Biogen continues to evaluate the efficacy, safety and tolerability of natalizumab EID through the prospective NOVA trial ( NCT03689972 ) with initial results expected in 2021. Biogen currently has more than 25 MS clinical trials underway including research on considerations around COVID-19 vaccination for people with MS.

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XTalks

JANUARY 26, 2024

Clinical trials have demonstrated the potential of CRISPR/Cas9 in this field. Personalized medicine: One of the most exciting prospects of CRISPR/Cas9 in oncology is its contribution to personalized medicine. By tailoring treatments based on an individual’s genetic makeup, it may allow for more effective and targeted therapies.

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The Pharma Data

OCTOBER 1, 2021

Bayer published today the results of its LEADER-75 (LowEr Administered Dose with highEr Relaxivity) study, demonstrating the clinical efficacy of a reduced dose of gadobutrol compared to a typical dose of gadoterate in patients undergoing a steady-state contrast-enhanced MRI of the CNS. mmol/kg) for CNS imaging. mmol/kg weight. “At

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The Pharma Data

MARCH 23, 2023

Darolutamide has already demonstrated efficacy and safety in nmCRPC with the Phase III ARAMIS trial, and in mHSPC with the Phase III ARASENS trial. The primary endpoint of this study is radiological progression-free survival (rPFS), measured by PSMA PET/CT assessed by independent central review.

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Drug Discovery World

APRIL 8, 2024

Ichnos Glenmark Innovation Ichnos Glenmark Innovation (IGI), an alliance between Ichnos Sciences and Glenmark Pharmaceuticals, shared pre-clinical data for its oncology asset ISB 2001, which is currently being tested in a Phase I clinical trial in relapsed/refractory multiple myeloma (r/r MM).

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The Pharma Data

OCTOBER 22, 2020

reflect the shared commitment of Gilead, government agencies and clinical trial investigators to advance well-tolerated, effective treatment options for the fight against COVID-19. The incidence of adverse events associated with Veklury was similar to placebo in the ACTT-1 trial. to 2.48; p=0.017).

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FDA Law Blog

FEBRUARY 28, 2022

Hearing from patients at the outset can help lead to better clinical trial designs, expedited patient recruitment, and ultimately greater acceptance of new medical devices! Finally, mark your calendars for the upcoming March 22, 2022 FDA webinar about this Guidance. The FDA webinar information can be found here.

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XTalks

AUGUST 30, 2022

Clinical research experts from the CRO Medpace shared insights about the operational and regulatory considerations for neuroscience trials with direct CNS administration. Why is it Difficult to Develop CNS Therapeutics?

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XTalks

FEBRUARY 10, 2021

Today’s authorization offers a new option for the thousands of individuals who experience snoring or mild sleep apnea,” said Malvina Eydelman, MD, director of the Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices in the FDA’s Center for Devices and Radiological Health, in a FDA news release. How it Works.

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The Pharma Data

AUGUST 15, 2021

The approval is based on results from the open-label Study 004 trial (N=61), where the major efficacy endpoint was overall response rate (ORR) in patients with VHL-associated RCC. The major efficacy endpoint for the treatment of VHL-associated RCC was ORR measured by radiology assessment using RECIST v1.1 WELIREG is the first HIF-2?

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XTalks

APRIL 6, 2021

The Harmony pulmonary valve is implanted using a thin catheter with a collapsed Harmony valve on the end. The catheter carrying the valve is inserted through a vein in the groin or in the neck into the right side of the heart and into the RVOT where it is placed into position.

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Drug Discovery World

APRIL 14, 2023

Carolyn R Bertozzi, PhD – Outstanding Achievement in Chemistry in Cancer Research Bertozzi is the Baker Family Director of Sarafan ChEM-H, the Anne T and Robert M Bass Professor in the School of Humanities and Sciences, Professor of Chemistry and, by courtesy, of Chemical and Systems Biology and of Radiology at Stanford University.

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The Pharma Data

NOVEMBER 9, 2021

Still, the recommended cure for molnupiravir grounded on the Phase 3 MOVe- OUT clinical trial would be 800 mg doubly daily for five days, If authorized or approved.

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The Pharma Data

NOVEMBER 6, 2020

director of the Office of Neurological and Physical Medicine Devices in the FDA’s Center for Devices and Radiological Health. This device was studied in a 30-day randomized, sham-controlled trial of 70 patients. Nightware is available by prescription only and is intended for home use.

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pharmaphorum

SEPTEMBER 14, 2021

In the European hospital setting, the first to digitise were the picture archiving systems (PACS) in radiology departments then electronic medical records (EMRs), patient administration systems and departmental IT flow work solutions (eg, laboratory information systems and radiology information systems).

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The Pharma Data

NOVEMBER 18, 2020

The California company said that clinical trials showed 100% of patients were able to perform the Lucira test in about two minutes. The trial results — delivered less than a year after researchers began working on the vaccine — shattered all speed records for vaccine development, the Times reported.

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Drug Discovery World

APRIL 16, 2023

DDW’s Megan Thomas rounds up highlights from Sunday 16 April at AACR 2023, from promising trial results for a personalised mRNA-based cancer vaccine to winners of lifetime achievement awards.

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The Pharma Data

DECEMBER 8, 2020

Under the Orphan Drug Act, FDA may provide grant funding toward clinical trial costs, tax advantages, FDA user-fee benefits, and seven years of market exclusivity in the United States following marketing approval by FDA.

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