Anebulo Pharmaceuticals Announces Positive Interim Data for ANEB-001 from Part B of its Phase 2 Clinical Trial for Acute Cannabinoid Intoxication

Lower doses of ANEB-001 reduced the negative effects of higher doses of THC Currently exploring delayed dosing to better understand real-world conditions AUSTIN, Texas–(BUSINESS WIRE)–Anebulo Pharmaceuticals, Inc. (Nasdaq: ANEB), a clinical-stage biopharmaceutical company developing novel solutions for people suffering from acute cannabinoid intoxication (ACI) and substance addiction (the “Company” or “Anebulo”), today announced positive interim … [Read more…]

The Worldwide Biotechnology Industry is Expected to Reach $2,234 Billion by 2027 – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Biotechnology Market Research Report by Technology (Cell-based Assays, Chromatography, and DNA Sequencing), Application, Region (Americas, Asia-Pacific, and Europe, Middle East & Africa) – Global Forecast to 2027 – Cumulative Impact of COVID-19” report has been added to ResearchAndMarkets.com’s offering. The Global Biotechnology Market size was estimated at USD 876.74 billion in 2021, USD … [Read more…]

Insights on the Epilepsy Monitoring Device Global Market to 2027 – Increasing Demand for Non-Invasive and Minimally Invasive Devices Presents Opportunities – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Epilepsy Monitoring Device Market Research Report by Product (Conventional Devices and Wearable Devices), End User, Region (Americas, Asia-Pacific, and Europe, Middle East & Africa) – Global Forecast to 2027 – Cumulative Impact of COVID-19” report has been added to ResearchAndMarkets.com’s offering. The Global Epilepsy Monitoring Device Market size was estimated at USD 480.45 … [Read more…]

Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent Vaccine Booster in Children 5 Through 11 Years of Age

NEW YORK & MAINZ, Germany–(BUSINESS WIRE)–Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced they have completed a submission to the U.S. Food and Drug Administration (FDA) requesting Emergency Use Authorization (EUA) of a 10-µg booster dose of the companies’ Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine for children ages 5 through 11 years of … [Read more…]

Children’s Hospital Los Angeles Identifies Molecular Markers to Increase Precision in Treatment of Retinoblastoma

New genes implicated in disease create new therapeutic targets and ability to assess disease severity. LOS ANGELES–(BUSINESS WIRE)–Retinoblastoma is a cancer of the eye that occurs in infants and toddlers and can lead to loss of vision, loss of one or both eyes, and even death. Unlike most tumors, these cannot be biopsied because of … [Read more…]

Atamyo Therapeutics Announces First Patient Dosed with ATA-100 Gene Therapy in LGMD-R9 Clinical Trial

First patient dosed with ATA-100 gene replacement therapy for LGMD-R9 On-going multicenter, Phase 1/2 study evaluating safety, pharmacodynamic and efficacy of ATA-100 EVRY, France–(BUSINESS WIRE)–Atamyo Therapeutics, a biotechnology company focused on the development of new-generation gene therapies targeting neuromuscular diseases, today announced the dosing with ATA-100 of a first patient in a phase 1/2 clinical … [Read more…]

FDA Trends for Computer System Validation (CSV) Compliance and Enforcement (Virtual Seminar) – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “4-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement” webinar has been added to ResearchAndMarkets.com’s offering. Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation. They will understand how to develop the most robust computer … [Read more…]

CatalYm Receives FDA IND Clearance to Expand Development of Visugromab in Advanced Cancer Patients into the U.S.

MUNICH, Germany–(BUSINESS WIRE)–CatalYm today announced that it has received Investigational New Drug (IND) clearance from the United States Food and Drug Administration (FDA) to expand its ongoing Phase 2 clinical program to include clinical trial centers in the U.S. The ongoing GDFATHER-2 program (GDF-15-neutralizing antibody-mediated human effector cell relocation) is evaluating the company’s lead candidate, … [Read more…]

Middle East and Africa Travel Vaccines Market Analysis/Forecast Report 2022-2028 Featuring Abbott, Bharat Biotech, GlaxoSmithKline, Merck & Co, Novartis, Pfizer, & Sanofi – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Middle East and Africa Travel Vaccines Market Forecast to 2028 – COVID-19 Impact and Regional Analysis By Product and Application” report has been added to ResearchAndMarkets.com’s offering. The travel vaccines market in MEA is expected to grow from US$ 120.13 million in 2021 to US$ 167.76 million by 2028; it is estimated to … [Read more…]

Global Pernicious Anemia Market Report 2022-2028: Increasing Prevalence of Autoimmune Conditions Driving Sector Growth – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Global Pernicious Anemia Market Research and Forecast, 2022-2028” report has been added to ResearchAndMarkets.com’s offering. The global pernicious anemia diagnosis and treatment market is anticipated to grow at a significant CAGR of 7.1% during the forecast period. Pernicious anemia is a disease in which the formation of red blood cells becomes slow due … [Read more…]