Rose became acquainted with Patient Worthy after her husband was diagnosed with Acute Myeloid Leukemia (AML) six years ago. During this period of partial remission, Rose researched investigational drugs to be prepared in the event of a relapse. Her husband died February 12, 2021 with a rare and unexplained occurrence of liver cancer possibly unrelated to AML.
An announcement by Pfizer was recently published in Biospace outlining the results of BASIS its Phase 3 clinical trial (NCT03938792). The drug being studied, marstacimab, met its primary endpoints…
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Experimental Therapy for Hemophilia Meets Phase 3 Trial Endpoints
Céline Dion’s new milestone is her first-ever film, Love Again, which she stars in while living with a rare disease called stiff person syndrome. Céline expressed her wishes that…
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Celine Dion Isn’t Slowing Down Despite Stiff Person Syndrome Diagnosis
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A court in Zabbar, Malta found the parents of seven-year-old Victoria guilty of her death by negligence. The court also determined that the system had failed the child by…
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Parents in Malta Handed a Prison Sentence for the Death of Daughter Who Died of Aplastic Anemia
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In Japan researchers at the Juntendo University have discovered that when ECHS1 enzyme variations of mitochondrial enoyl-CoA hydratase short chain 1 (ECHS 1) do not function properly, they cause…
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A High-Efficiency Assay with Rapid Mitochondrial Disease Diagnosis
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WebMD recently carried a story about a young woman who, after nine years of wheelchair confinement caused by a rare metabolic disease with no name, was able to walk…
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Drug Repurposing: Saving Rare Disease Patient Lives
The FDA has approved the drug Ayvakit developed by the biotechnology company Blueprint Medicines for the treatment of indolent systemic mastocytosis. According to an article in BiopharmaDive, Ayvakit had been…
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The FDA Has Approved Ayvakit for the Treatment of Indolent Systemic Mastocytosis
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As clinicians and scientists continue to delve into RNA sequencing benefits, they are learning how RNA sequencing provides insights for people with rare genetic conditions. The learning experience will provide…
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RNA Sequencing: Hope for Improved Rare Disease Diagnosis
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Fierce Biotech recently carried an article about the death of Terry Horgan. Terry was a 27-year-old Duchenne muscular dystrophy (DMD) patient and the brother of the CEO of the…
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Duchenne Muscular Dystrophy Patient Dies in Gene Therapy Trial
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John knew from an early age that he not only loved music but had confidence in his musical ability. However, there was another very troubling issue in his life. John…
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This Spinal Muscular Atrophy Patient Established a Nonprofit for Disabled Artists
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The biotechnology company Anixa Biosciences, Inc. together with the Moffitt Cancer Center, issued a press release on May 22nd stating that the second patient had begun treatment as part…
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Ovarian Cancer: Second Patient Treated with Novel CAR-T in Trial
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Thirty-year-old Brendan O’Reilly was told that his rare disease affects only one person in 250,000. He was also told that he is lucky to be alive. Brendan’s symptoms confused…
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Acute Disseminated Encephalomyelitis Can be Confused for a Stroke
The Chow family was told that their 33-year-old daughter, Brittney, would have to wait about twelve years for a kidney transplant. There were currently no kidneys available for transplantation. Elizabeth…
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There Is No Limit to What Some Mothers Will Do For Their Children.
In March the FDA’s expert advisers voted 11 to 2 in favor of approving Roche’s antibody drug Polivy to treat lymphoma patients. According to an article in BiopharmaDive, the decision…
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The FDA Approves Roche’s Antibody Drug Polivy to Treat Lymphoma Patients
The safety, pharmacokinetics (absorption), and tolerability of the investigational eIF2B activator ABBV-CLS-7262 is being evaluated in a Phase 1b clinical study to treat patients with Vanishing White Matter (VWM) Disease.…
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ABBV CLS 7262 is Being Evaluated as a Potential Treatment for Vanishing White Matter Disease in the Brain
PhRMA Public Affairs recently carried the good news that Governor Holcomb of Indiana has joined the governors of Arkansas and West Virginia by signing a law aptly named 'Share the…
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Indiana Legislature Passes Bill Protecting Patients from Paying More Than Their Insurers
This week PR Newswire carried an announcement by the biotechnology company Immunic Inc. of preclinical data confirming that Vidofludimus Calcium (IMU 838) may be a Nurr 1-Activator reinforcement. Immunic is…
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Immunic Inc. Announces Promising Pre-Clinical Findings for Multiple Sclerosis
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For patients who were given a diagnosis of advanced, inoperable (unresectable) biliary tract cancer, an article appeared in Healio with some encouraging news. Gemcitabine and cisplatin drugs have…
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A Glimmer of Hope for Patients with Advanced Biliary Tract Cancer
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Omisirge (omidubicel) is the first allogeneic (from a donor) product for SCT that has been the recipient of FDA approval. The FDA's nod moves Omisirge into the realm of…
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New Cell Therapy Approved by the FDA to Reduce Risk of Infection After Transplant
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The damage caused by cocaine can sometimes be misdiagnosed as a rare disease: granulomatosis with polyangiitis. Cocaine use has been increasing in America and the UK, resulting in serious…
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Damage from Cocaine Abuse can be Misdiagnosed as Granulomatosis with Polyangiitis
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Compassion [kuhm-pash-uhn] noun A feeling of deep sympathy and sorrow for another who is stricken by misfortune, accompanied by a strong desire to alleviate the suffering. Compassion Corner is a…
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Compassion Corner: Compassion Should be Reciprocal: The Rising Suicide Rate of Physicians and Nurses
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In the last decade, NAFLD in pregnancy has nearly tripled in concert with the worldwide increase in diabetes. Mayo Clinic reports that NAFLD in general affects one-fourth of the…
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Non-Alcoholic Fatty Liver Disease (NAFLD) in Pregnancy has Nearly Tripled in the Past Ten Years
Gene therapy has seemed out of reach for decades. Yet advocates have considered it a way to have damaged or missing genes restore dystrophin and other proteins. Doctors and advocates…
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Sarepta’s Duchenne Gene Therapy Drug Cleared for Accelerated Approval
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A Business Wire Press Release on April 26, 2023, announced positive interim clinical data on an investigational RNAi therapeutic. Alnylam Pharmaceuticals and its partner Regeneron Pharmaceuticals heralded interim results…
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Positive Interim Findings in Alzheimer’s Clinical Trial
Canada’s unemployment rate is at a record low. Industries have recovered 126% of the jobs lost by the pandemic. On the health front, scientific knowledge and the ability to…
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Canada Will Provide $1.5 Billion to Provinces to Support Rare Disease Programs
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For patients with refractory or relapsed KMT2A rearrangement or NPM1-mutations, the AUGMENT 101 study of the investigational menin inhibitor revumenib yielded impressive results. According to an article in MedicalXpress,…
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Advanced Leukemia: Test of Oral Revumenib Brought Impressive Results