Top 5 Rare Disease News of the Week—September 9, 2018
SEPTEMBER 15, 2018
Rare Disease Report® Editorial Staff
#5 Accelerated Approval Denied & Pivotal Study Underway for Pompe Disease Treatment, AT-GAA
The decision followed a Type C meeting between the FDA and Amicus that discussed the regulatory path for AT-GAA. The upcoming, single pivotal study will compare AT-GAA to the current standard of care (alglucosidase alfa, an enzyme replacement therapy) and will serve as the study to support full approval.
Approximately 100 participants with Pompe disease are anticipated to enroll in the trial, which will include a population of both ERT-switch patients and ERT treatment-naïve patients. A 6-minute walk with a primary treatment period of up to 12 months will serve as the primary endpoint.
Read more about the denied accelerate approval and pivotal study underway for Pompe disease treatment, AT-GAA.
#4 Rhabdomyosarcoma Cellular Origins and Therapeutic Vulnerabilities UncoveredInvestigators from St. Jude Children’s Research Hospital have recently made strides in the fight against rhabdomyosarcoma, a rare childhood sarcoma that occurs in approximately 350 children and adolescents nationwide annually.
In the most comprehensive analysis of a common pediatric solid tumor to date, the team has identified weaknesses to target in the rare cancer, leading to a promising precision medicine treatment that has already hit clinical trials.
“Rhabdomyosarcoma patients with recurrent or metastatic disease represent a real clinical challenge with few patients achieving long-term survival,” Elizabeth Stewart, MD, co-first author of the study, said to Rare Disease Report®. “Since there are not a lot of known druggable mutations in rhabdomyosarcoma, we aimed to identify tumor vulnerabilities that extend beyond somatic mutations in the genome.”
As additional therapeutic vulnerabilities are increasingly identified due to tumor-specific epigenetic perturbations that lead to altercations in gene expression, personalized cancer therapies aimed at targeting somatic mutations in patient tumors are increasingly entering into treatment approaches.
Since genomic and epigenomic changes ultimately manifest in the tumor proteome and phosphoproteome, Dr. Stewart and her team utilized transcriptomic, epigenomic, and proteomic/phosphoproteomic data to shed light on rhabdomyosarcoma’s cellular origins and therapeutic vulnerabilities.
Read more about the uncovered cellular origins and therapeutic vulnerabilities in rhabdomyosarcoma.
#3 Telavancin: Promising Treatment Option for MRSA in Cystic Fibrosis Patients?Methicillin-resistant Staphylococcus aureus continues to plague patients in the health care and community setting, as well as the providers who treat them. When acquired in patients with cystic fibrosis, clinical outcomes are known to be even worse, resulting in an increased rate of declined respiratory function as well as infections that can have severe, and sometimes deadly, consequences.
For the first time, however, investigators have found that telavancin—a drug currently used to treat skin infections and hospital-acquired pneumonia—has potent in vitroactivity and low resistance development potential when used against S aureusisolates in patients with cystic fibrosis, making it a promising potential treatment option for these patients.
“Telavancin (TLV) is a lipoglycopeptide antibiotic approved by the US Food and Drug Administration (FDA) in 2009 for the treatment of complicated skin and skin structure infections and in 2013 for the treatment of cases of nosocomial pneumonia. However, its application for the treatment of CF-MRSA pneumonia infections was not known, so our studies are contributing to extend the application of TLV for CF treatment,” Adriana E. Rosato, PhD, associate professor in the department of Pathology and Genomic Medicine at Houston Methodist Research Institute told our sister publication Contagion®.
Read more about how telavancin may be a promising treatment option for MRSA in cystic fibrosis patients.
#2 Fast Track Designation Granted to Idiopathic Pulmonary Fibrosis Treatment, Pamrevlumab
The US Food and Drug Administration (FDA) has granted a fast track designation to FibroGen, Inc’s pamrevlumab for the treatment of patients with idiopathic pulmonary fibrosis (IPF).
“This Fast Track designation reflects recognition of the great need for a new therapeutic to help patients diagnosed with IPF to reduce the burden and progression of this debilitating disease and another positive step in developing pamrevlumab for the treatment of IPF,” Elias Kouchakji, MD, senior vice president of Clinical Development and Drug Safety at FibroGen, said in a recent statement. “We look forward to advancing pamrevlumab into phase 3 studies early next year.”
Data from a randomized, double-blind, placebo-controlled phase 2 clinical trial served as the basis for the designation. The main objective of the trial was to see if the treatment improved lung function; to do this, investigators measured the change in forced vital capacity (FVC) at weeks 12, 24, 36, and 48 and compared that data with the beginning of the trial.
Secondary objectives for the trial were to assess the progression of lung fibrosis, which they measured by using quantitative high-resolution computed tomography at weeks 24 and 48. The treatment’s safety and impact on quality of life were also evaluated.
Read more about the FDA;s fast track designation to IPF treatment, pamrevlumab.
#1 New Look at Gene Expression in the Brain May Offer Clue to Treating Huntington's DiseaseNew research conducted by scientists from Lund University in Sweden is shedding new light on Huntington’s disease and the potential for new therapies for this and other neurodegenerative diseases.
The progressive brain disorder, Huntington’s disease (HD), typically has an onset in adulthood and is marked by uncontrolled movements, emotional problems, and cognitive loss. The condition is caused by mutations in the HTT gene, which provides instructions for the production of a protein called huntingtin that plays an important role in the brain’s nerve cells. This mutation leads to a buildup of protein aggregates in the nerve cells of the brain, thereby impairing their normal functions.
Autophagy is the biological process by which nerve cells break down and remove protein aggregates, a process which is disrupted in individuals with neurodegenerative diseases (NDDs), such as HD, Parkinson’s, and Alzheimer’s. In a recent study published in the journal Cell Reports, investigators set out to find if activating the process of autophagy can reverse the accumulation of the protein Argonaute-2 (AGO2) in neurons.
“We know very little about why protein aggregates arise or in what way they are involved in the development of the disease,” said the study’s lead author and head of the university’s Molecular Neurogenetics Jakobsson Lab, Johan Jakobsson, PhD, in a recent statement. “However, our study shows that expression of the mutated huntingtin gene impairs the nerve cells’ ability to break down and recycle cellular material, which results in an accumulation of the protein AGO2.”
By studying cell culture, mouse models, and human tissue from deceased HD patients, the investigators observed that AGO2 accumulation results in an increase in levels of microRNA (miRNA) levels, and that changes in the autophagy mechanism also resulted in extensive changes in microRNA activity. Their findings, according to the authors, indicate that impaired autophagy in Huntington’s disease and other diseases not only effects protein aggregation but also “directly contributes to global alterations of intracellular post-transcriptional networks.”
Read more about how a new look at gene expression in the brain may offer clues to treating Huntington’s disease.
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