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Clinical Trial News

Celltrion's SteQeyma gets EC approval for inflammatory diseases

The European Commission approved Celltrion's SteQeyma, a biosimilar to Stelara, for chronic inflammatory conditions. SteQeyma, effective against IL-12 and IL-23, offers subcutaneous and intravenous formulations. It matches Stelara in efficacy and safety, marking Celltrion's seventh EU-approved biosimilar, enhancing access to affordable biologics.

Izotropic Plans Regulatory Approval for IzoView Breast CT in U.S. and EU

Izotropic Corporation is advancing its regulatory strategy to launch IzoView, a breast CT imaging system, in the U.S. and EU. The device is aimed at diagnosing breast cancer in patients with dense breast tissue, utilizing a clinical study to prove its efficacy alongside digital breast tomosynthesis.

Wegovy Helps Patients With Heart Failure Avoid Heart Attack, Stroke

Wegovy (semaglutide) reduces major adverse cardiac events by 28% in heart failure patients, regardless of ejection fraction type, and also lowers heart disease-related and all-cause mortality.

No Link Found Between Migraines, Parkinson's Disease

A study involving 39,000 women, including 7,300 with migraines, found no increased risk of Parkinson's disease among those with migraines. Published in the journal *Neurology*, the research suggests no association between migraines and Parkinson's, regardless of migraine frequency or aura presence.

mRNA Cancer Vaccine Clinical Trials Insight

The global mRNA cancer vaccines clinical trials and market future outlook for 2024 highlights over 60 vaccines in clinical trials, with the highest phase being Phase III. The US and China dominate the trials, with skin cancer vaccines leading. mRNA vaccines offer a personalized, targeted approach to cancer treatment, leveraging the body's immune system to combat cancer cells. They are being explored as combination therapies and for preventing cancer recurrence, with early results showing promise.

Lixte Biotechnology faces Nasdaq delisting over equity ...

Lixte Biotechnology Holdings, Inc. (NASDAQ:LIXT) received a Nasdaq non-compliance notice for falling below the $2.5M stockholders' equity requirement. It has 45 days to submit a compliance plan, with a possible 180-day extension. The company is exploring options to regain compliance, while its shares continue trading. Recent changes include a shift to equity-based director compensation and a clinical trial agreement with the Netherlands Cancer Institute for cancer drug LB-100.

Moderna Receives U.S. FDA Approval for Updated COVID-19 Vaccine Targeting KP.2 Variant of SARS-CoV-2

Moderna's updated COVID-19 vaccine targeting KP.2 variant of SARS-CoV-2 has been approved by the U.S. FDA for individuals 12 years and above, with EUA granted for those 6 months through 11 years. The vaccine aims to prevent COVID-19 and is expected to be available soon.

Bayer Initiates Phase II Study of Soluble Guanylate Cyclase Activator (BAY3283142) in Patients with Chronic Kidney Disease

Bayer starts Phase II ALPINE-1 study of BAY3283142, an sGC activator for chronic kidney disease, aiming to provide a new treatment option for cardiovascular diseases.

Molecule One-Pager: KT-474 (SAR444656)

Explains Phase II drug metabolism, summarizes common enzyme-mediated bioconjugation reactions, and discusses examples of Phase II transformations and their impact on drug pharmacology.
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