Anna is from England and recently finished her undergraduate degree. She has an interest in medicine and enjoys writing. In her spare time she likes to cook, hike, and hang out with cats.
A recent study suggests an alternative procedure for delivering the drug nusinersen to patients being treated for spinal muscular atrophy. Although more research needs to be done to estabilish its…
Continue ReadingResearchers Find a New Way to Deliver Nusinersen to Patients with Spinal Muscular Atrophy
Two clinical trials have had their study protocols amended, announces Pfizer and Astellas Pharma. The Phase 3 trials, called ‘Arches’ and ‘Embark’, will investigate the safety and effectiveness of the…
Continue ReadingTwo Clinical Studies of Enzalutamide in Hormone-Sensitive Prostate Cancer Have Been Amended
Tetra Bio-Pharma has submitted several Orphan Drug Designation applications to the US Food and Drug Administration. The applications are on behalf of cannabinoids for the treatment of multiple rare forms…
Continue ReadingTetra Has Submitted Multiple Orphan Drug Applications For Cancers and Ocular Disease
A group of researchers studying the causes underlying myelodysplastic syndromes have found that HIF1A may play an important role in these conditions. For more detailed information, you can read the…
Continue ReadingA New Study Identifies a Possible Gene Linked to Myelodysplastic Syndromes
The National Institutes of Health (NIH) have granted the University of Alabama at Birmingham $8.9 million to fund research into an investigational drug for idiopathic pulmonary fibrosis. You can read…
Continue ReadingThe NIH Has Granted $8.9 million to Researchers Investigating a Drug For Idiopathic Pulmonary Fibrosis
The drug minocycline is a tetracycline antibiotic. Previous research using mouse models has indicated that it may have anti-inflammatory and antiapoptotic (prevents cell death) properties and may benefit some neurological…
Continue ReadingA Recent Study Has Found That Minocycline Doesn’t Benefit People with Angelman Syndrome
Two companies, Tolero Pharmaceuticals Inc. and AbbieVie, have agreed to collaborate to clinically research a potential combination therapy for relapsed or refractory acute myeloid leukaemia. The potential therapy is comprised…
Continue ReadingTwo Companies Are Collaborating to Develop a Combination Therapy For Acute Myeloid Leukaemia
The investigational drug AT132 has been awarded Regenerative Medicine Advanced Therapy designation for the treatment of X-linked Myotubular Myopathy by the United States FDA. You can read the source press…
Continue ReadingThe FDA Has Awarded Regenerative Medicine Advanced Therapy Designation to an Experimental Drug for X-Linked Myotubular Myopathy
Two studies have looked into the long-term effects of subthalamic deep brain stimulation as a treatment for Parkinson’s disease. For more detailed information on this topic, you can find the…
Continue ReadingTwo Studies Investigated the Long-Term Effects of Subthalamic Deep Brain Stimulation as a Treatment for Parkinson’s Disease
The speciality pharmaceutical company Tikomed has announced that the UK Medicines and Healthcare Products Regulatory Agency has granted the company permission to go ahead with a Phase 2 clinical study.…
Continue ReadingTikomed Has Received Permission to Carry Out a Study of Their Experimental Drug for ALS in the UK
According to a press release from Eisai Inc. and Merck (also known as MSD), Lenvima®(lenvatinib) has been approved by the United States FDA as a first-line treatment for patients…
Continue ReadingA New Drug Has Been Approved For the Treatment of Unresectable Hepatocellular Carcinoma
A team of researchers led by Constantinos Koshiaris from the University of Oxford have recently published a study that investigated the best way to identify multiple myeloma through blood tests.…
Continue ReadingResearchers Have Found Which Common Blood Tests are the Most Effective for Identifying Multiple Myeloma
The United States FDA has awarded Fast Track Designation to the investigational drug AVB-S6-500 for the potential treatment of platinum-resistant recurrent ovarian cancer. You can find out more detailed information…
Continue ReadingThe FDA Has Awarded Fast Track Designation to an Investigational Drug For Certain Forms of Ovarian Cancer
According to The Times of Israel, a group of researchers believe they have found the origin of what could lead to a treatment for amyotrophic lateral sclerosis. Given the debilitating effect…
Continue ReadingIsraeli Scientists Making Major Strides in ALS Treatment Research
Several organisations are collaborating to develop a gene therapy that targets cystic fibrosis. Boehringer Ingelheim, Imperial Innovations, Oxford BioMedica, and the UK Cystic Fibrosis Gene Therapy Consortium will work…
Continue ReadingOrganisations are Collaborating to Develop a Gene Therapy for Cystic Fibrosis
The healthcare technology company RDMD was founded by Onno Faber, who has himself been diagnosed with a rare disorder. RDMD, which describes itself as “dedicated to accelerating research” with…
Continue ReadingA Man Who Set Up a Healthcare Company After Being Diagnosed with Neurofibromatosis Has Secured $3 Million Funding
Takeda Pharmaceutical Company Limited and Ovid Therapeutics have released an overview of the clinical development program for TAK-935/OV935, an investigational drug that is being developed as a potential anti-epileptic…
Continue ReadingTakeda and Ovid Have Provided an Update on the Clinical Development Program for an Investigational Anti-Epileptic Drug
The US Food and Drug Administration (FDA) has released a statement outlining its plans to promote patient voices in the development and regulation of medical products. You can find more…
Continue ReadingThe FDA Wants to Listen to Patient Voices in Medical Development and Regulation
Researchers have found that an artificial intelligence (AI) system is able to recommend patient referrals for over fifty eye conditions as accurately as world-leading doctors. The project is part of…
Continue ReadingArtificial Intelligence Can Accurately Recommend Patient Referrals For Eye Conditions
The United States FDA has approved the first generic version of EpiPen and EpiPen Jr (epinephrine). The approval was granted to Teva Pharmaceuticals USA, who will now be able to…
Continue ReadingThe FDA Has Approved the First Generic Version of EpiPen
Two companies, GtreeBNT and YuYang DNU, will collaborate in a joint venture to develop the investigational drug RGN-137 for the treatment of epidermolysis bullosa. For more details, you can read…
Continue ReadingTwo Companies are Collaborating to Develop an Investigational Drug for Epidermolysis Bullosa
A recent study published in the journal Clinical Cancer Research has found that a certain protein called KIM-1 may be able to predict renal cell carcinoma up to five years before…
Continue ReadingResearchers May be Able to Predict Kidney Cancer Years in Advance
The US FDA has awarded Breakthrough Therapy Designation to encorafenib (braftoviTM) combined with binimetinib (mektovi®) and cetuximab for use as an investigational (not FDA-approved) treatment of BRAFV600E–mutant metastatic colorectal cancer.…
Continue ReadingAn Experimental Drug Combination Treatment for Certain Bowel Cancers Has Been Granted Breakthrough Therapy Designation
A Biologics License Application for ElzonrisTM (also known as tagraxofusp and SL-401) for the treatment of blastic plasmacytoid dendritic cell neoplasm has been accepted for filing by the United States FDA.…
Continue ReadingThe FDA Have Granted Priority Review to Elzonris for the Treatment of Blastic Plasmacytoid Dendritic Cell Neoplasm
Researchers are exploring a new diagnostic method that could be applied to newborn screening for certain inherited diseases and monitoring of HIV patients. For more detailed information, you can click…
Continue ReadingEpigenetic Technology Could Become Useful in Newborn Screening for Primary Immunodeficiency and Monitoring HIV
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