Jessica Lynn has an educational background in writing and marketing. She firmly believes in the power of writing in amplifying voices, and looks forward to doing so for the rare disease community.
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Those living with rare diseases or conditions often face difficulty in finding treatment options - or even spurring researchers to make headway within their disease states. To combat this and…
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Paxalisib Earns Orphan Drug Designation for Atypical Teratoid Rhabdoid Tumors
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In the United States, the Orphan Drug Act was established to incentivize drug developers and other stakeholders to begin developing therapies for rare diseases. Orphan Drug designation is now granted…
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Evorpacept for AML Earns Orphan Drug Designation
Rituximab has been used to treat patients with cancers such as non-Hodgkin’s lymphoma (NHL), and various autoimmune diseases. Recently, a study sought to understand whether rituximab treatment would be safe…
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Rituximab Safe for Pediatric MG Patients, Study Says
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Sometimes, certain health conditions can increase the risk of developing other conditions. According to a new research study, this may be the case with porphyria and hepatocellular carcinoma. An article…
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Porphyria Increases Liver Cancer Risk by 5%, Study Shows
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At the end of June 2022, biopharmaceutical company InflaRx N.V. (“InflaRx”) shared via press release that its product vilobelimab recently earned Orphan Drug designation in both the United States…
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Vilobelimab for Pyoderma Gangrenosum Earns Orphan Drug Designation
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On July 7, 2022, biotechnology company Akari Therapeutics, Plc ("Akari") shared via news release that the first patient in its clinical trial has completed their course of treatment. Within…
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First Patient with HSCT-TMA Completes Nomacopan Treatment in Phase 3 Trial
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Don't forget to check out Parts 1 and 2 of our interview, where we discussed APFED, eosinophilic esophagitis (EOE), and Lori's diagnostic process. Today, in the final portion of the interview, we're…
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INTERVIEW: The Charge to Raise Eosinophilic Esophagitis Awareness (Pt. 3)
Did you know that July is widely considered to be Sarcoma Awareness Month? During this month, many stakeholders - from patients to researchers - aim to raise awareness of sarcomas,…
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July 13th is GIST Awareness Day!
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According to Cure Today, the U.S. FDA granted Orphan Drug designation to MB-106, a novel CAR-T cell therapy designed to treat Waldenström macroglobulinemia (WM). In the United States, Orphan…
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MB-106 for WM Granted Orphan Drug Designation
In a news release, biopharmaceutical company Fulcrum Therapeutics, Inc. ("Fulcrum") shared that the first patient was dosed in the Phase 3 REACH study. Within the study, researchers are evaluating…
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First Patient Enrolled in Losmapimod Trial for FSHD
If you're just joining us, don't forget to take a look at Part 1 of this interview. In Part 1, we discussed Lori and Mary Jo Strobel, what eosinophilic esophagitis (EOE) is,…
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INTERVIEW: The Charge to Raise Eosinophilic Esophagitis Awareness (Pt. 2)
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Food has the power to change lives, to spark connection and understanding, to raise cultural awareness, and to bring people together. Nobody knows this better than 48-year-old Lori, who spent…
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INTERVIEW: The Charge to Raise Eosinophilic Esophagitis Awareness (Pt. 1)
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In a press release on the company website, biopharmaceutical company AbbVie shared that preliminary data was available regarding navitoclax, an investigational therapy, for individuals with primary myelofibrosis. The data…
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Preliminary Data Available on Navitoclax for Myelofibrosis
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The ENDO 2022 Annual Congress took place from June 11-14, 2022. During the Congress, stakeholders met to discuss care, treatments, and research within endocrinology. In a news release from…
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ICYMI: Evaluating Sogroya for Pediatric Growth Hormone Deficiency
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In 2019, Courtney and Michael Henderson welcomed the newest member of their family – their son Luke. They were thrilled at this new addition, who they say is one…
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October 8: Golf for Phelan-McDermid Syndrome
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From May 13-18, 2022, the American Thoracic Society (ATS) held its Annual Meeting, where researchers and stakeholders discussed research, patient care, and public health trends within the fields of…
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ICYMI: Midodrine Increases PAH Therapy Tolerability
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In many cases, orally administered PDE5 inhibitors – such as Cialis, Levitra, and Stendra – have been used to treat erectile dysfunction. These vasodilating drugs were found to be…
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PDE5 Inhibitors Could Enhance Esophageal Cancer Treatment
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The number of Alzheimer’s disease diagnoses has been rising rapidly over the last few decades. Today, an estimated 6.5 million Americans alone are living with this disease. Yet there…
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New Alzheimer’s Research Could Help with Drug Development
The American Society of Clinical Oncology (ASCO) Annual Meeting (“ASCO 22”) took place this year from June 2nd through the 6th, 2022. During this Annual Meeting, stakeholders within the…
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Early Findings Show DS-6000 Benefits for Ovarian Cancer, RCC
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Have you ever heard of Orphan Drug designation? In the United States, this designation is granted to drugs or biologics that intend to treat, prevent, or diagnose rare diseases…
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VBI-1901 for Glioblastoma Granted Orphan Drug Designation
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For some patients with NF2-deficient malignant pleural mesothelioma (MPM), their cancer is unresectable, meaning that it cannot be surgically removed. Finding a way to better treat and assist these…
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IK-930 for NF2-deficient Malignant Pleural Mesothelioma Earns Fast Track Designation
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Sometimes, doctors choose to treat a certain condition with a specific medicine or class of medicines. But what happens when that medicine causes unintended and potentially harmful reactions? For…
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Can Immune Checkpoint Inhibitors Worsen Proteinuria in mRCC?
The last approved treatment option for Pompe disease in Europe was given approval in 2006, so 16 years ago. However, the European Commission (EC) recently approved a new therapeutic…
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EC Approves Nexviazyme for Pompe Disease
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Pulmonary arterial hypertension (PAH) is a chronic and progressive form of high blood pressure in the lungs which can result from a number of causes: HIV, sickle cell disease,…
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Experimental Stem Cell Treatment Benefits Girl with PAH
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Sometimes, it can be difficult to diagnose amyotrophic lateral sclerosis (ALS), a progressive neurological disease which causes nerve cell (motor neuron) death in the brain, brain stem, and spinal…
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Could a Muscle Biopsy Lead to Earlier ALS Diagnoses?