The Genetic and Developmental Processes Underlying Pachygyria are Explored in a Recent Study
ColiN00B / Pixabay

The Genetic and Developmental Processes Underlying Pachygyria are Explored in a Recent Study

A recently published paper called ‘Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration’ outlines new research into the genetic basis of…

Continue Reading The Genetic and Developmental Processes Underlying Pachygyria are Explored in a Recent Study
Possible Breakthrough Therapy for Premature Babies with Bronchopulmonary Dysplasia
https://pixabay.com/en/baby-care-child-cute-hand-face-20339/

Possible Breakthrough Therapy for Premature Babies with Bronchopulmonary Dysplasia

According to 9News, Harry Campbell was born very premature at 27 weeks. Not only this, but his dimensions were almost unfathomable. Harry was able to fit into the palm of…

Continue Reading Possible Breakthrough Therapy for Premature Babies with Bronchopulmonary Dysplasia
A Clinical Trial of Gemcabene in Paediatric Patients with Non-Alcoholic Fatty Liver Disease Has Been Stopped Following Safety Concerns
ernestoeslava / Pixabay

A Clinical Trial of Gemcabene in Paediatric Patients with Non-Alcoholic Fatty Liver Disease Has Been Stopped Following Safety Concerns

Gemphire Therapeutics Inc. has been recommended to stop a clinical trial by the Data and Safety Monitoring Board at Emory University School of Medicine. The clinical trial, which ran into…

Continue Reading A Clinical Trial of Gemcabene in Paediatric Patients with Non-Alcoholic Fatty Liver Disease Has Been Stopped Following Safety Concerns

Results from a Phase 3 Study of Recorlev as a Potential Treatment for Cushing’s Syndrome Have Been Released

The top-line results of a pivotal Phase 3 study investigating the drug recorlevTM (levoketoconazole) in patients with endogenous Cushing’s syndrome have been released. The source article, which contains more detailed information,…

Continue Reading Results from a Phase 3 Study of Recorlev as a Potential Treatment for Cushing’s Syndrome Have Been Released
Orphan Drug Status Has Been Awarded to an Investigational Drug For the Treatment of Stomach Cancer
Free-Photos / Pixabay

Orphan Drug Status Has Been Awarded to an Investigational Drug For the Treatment of Stomach Cancer

An investigational drug called ALT-P7 is being developed as a potential medicine for certain forms of cancer. The drug has received Orphan Drug Designation for the treatment of gastric cancer…

Continue Reading Orphan Drug Status Has Been Awarded to an Investigational Drug For the Treatment of Stomach Cancer
Guidelines for Rare Pregnancy-Related Cancers Released for the First Time
Source: Pixabay

Guidelines for Rare Pregnancy-Related Cancers Released for the First Time

According to a story from Newswise, an organization called the National Comprehensive Cancer Network (NCCN) has recently released treatment guidelines for a rare type of cancer that can affect women…

Continue Reading Guidelines for Rare Pregnancy-Related Cancers Released for the First Time
New Study Suggests That Fertility Treatment Doesn’t Increase Risk of Breast, Uterus, or Ovarian Cancer
Hans / Pixabay

New Study Suggests That Fertility Treatment Doesn’t Increase Risk of Breast, Uterus, or Ovarian Cancer

According to a story from whtc.com, a recent study from the UK is calling into question the widely held belief that fertility treatments could increase the risk of ovarian cancer,…

Continue Reading New Study Suggests That Fertility Treatment Doesn’t Increase Risk of Breast, Uterus, or Ovarian Cancer

The FDA Has Granted Orphan Drug Status to an Experimental Drug to Treat Amyloidosis

The US Food and Drug Administration (FDA) has awarded Orphan Drug Designation to the experimental drug ALN-TTRsc02. Alnylam Pharmaceuticals Inc. is developing ALN-TTRsc02 as a possible treatment for transthyretin-mediated amyloidosis.…

Continue Reading The FDA Has Granted Orphan Drug Status to an Experimental Drug to Treat Amyloidosis
For the First Time in 30 Years: A New Advancement in Rhabdomyosarcoma Treatment
https://pixabay.com/en/baby-care-child-cute-hand-face-20339/

For the First Time in 30 Years: A New Advancement in Rhabdomyosarcoma Treatment

  According to MedPage Today, a phase III study showed that 6 additional months of chemotherapy for maintenance led to a sizable increase in the 5-year overall survival rate for…

Continue Reading For the First Time in 30 Years: A New Advancement in Rhabdomyosarcoma Treatment
First Major Treatment Advance for PV Has Been Approved by the FDA
Source: pixabay.com

First Major Treatment Advance for PV Has Been Approved by the FDA

  According to BioSpace, a new treatment for pemphigus vulgaris (PV) has been recently approved by the U.S. Food and Drug Administration. The treatment, Rituxan (rituximab), is geared towards adults who have…

Continue Reading First Major Treatment Advance for PV Has Been Approved by the FDA
Orphan Drug Designation Has Been Awarded to Selumetinib for the Treatment of Neurofibromatosis Type 1
Source: Pixabay.com

Orphan Drug Designation Has Been Awarded to Selumetinib for the Treatment of Neurofibromatosis Type 1

The European Medicines Agency has awarded Orphan Drug designation to selumetinib for the treatment of neurofibromatosis type 1. You can read the source press release here, on Merck’s website. About…

Continue Reading Orphan Drug Designation Has Been Awarded to Selumetinib for the Treatment of Neurofibromatosis Type 1
Drug Label Expanded in the UK for Treating Rare Inflammatory Diseases
byrev / Pixabay

Drug Label Expanded in the UK for Treating Rare Inflammatory Diseases

According to a story from Hospital Healthcare Europe, The European Medicines Agency approved Kineret last year, an anti-inflammatory drug developed by Sobi. In the UK, Kineret is an approved treatment…

Continue Reading Drug Label Expanded in the UK for Treating Rare Inflammatory Diseases