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Fetal hemoglobin increases safely with increased hydroxyurea in infants with sickle cell anemia

Meghna Dua, MD, Department of Global Pediatric Medicine, St. Jude Children’s Research Hospital, presented data from her team’s findings regarding hydroxyurea dosing in very young children with sickle cell disease (SCA) during the American Society of Hematology (ASH) Annual Meeting and Exposition. With little published research on infants’ tolerance to hydroxyurea dose escalation, Dua and …

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Pyruvate kinase activators may benefit vaso-occlusive crisis in sickle cell disease

A pair of pyruvate kinase (PKA) activators have been linked to increased oxygen affinity and reduced propensity for red blood cell sickling in patients with sickle cell disease in vitro, according to new findings. In data presented at the 2022 Annual Meeting of the American Society of Hematology (ASH) in New Orleans this week, a …

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Arganine therapy shows positive impacts on sickle cell disease in ASH 2022 data

People with sickle cell disease (SCD) present to the emergency department (ED) and are often hospitalized, most often for episodes of vaso-occlusive pain (VOE). These episodes, also called “pain crises” because of the intense pain experienced by patients, cause acute arginine (Arg) deficiency. Arg supplementation has shown positive effects on blood pressure, cardiopulmonary function and …

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A new 'heart attack on a chip' could serve as a test bed for developing personalized drugs

A new ‘heart attack on a chip’ could serve as a test bed for developing personalized drugs

Researchers from the Alfred E. Mann Department of Biomedical Engineering at the University of Southern California have developed a “heart attack on a chip,” a device that could one day serve as a test bed for developing new heart drugs and even personalized drugs. “Our device replicates some key features of a heart attack in …

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Despite progress, government can better protect patients from harmful stem cell therapies

Despite progress, government can better protect patients from harmful stem cell therapies

In 2015, a 78-year-old Florida woman suddenly lost sight in both eyes after receiving stem cell treatment for macular degeneration. The therapy she underwent at a clinic involved a unique type of eye injection containing stem cells made from body fat. When her ophthalmologist examined her later, he saw chunks of blood floating in her …

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Increasing production of custom immune cells for drug development and testing

Increasing production of custom immune cells for drug development and testing

To prevent animal testing and create even more accurate ways to test therapeutics, the pharmaceutical industry is increasingly turning to human immune cells. However, the availability of cells like these has been limited to date. Now, Fraunhofer researchers have succeeded in taking the production of personalized immune cells from the laboratory to the industrial level. …

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Harmful gut bacteria co-opt genetic susceptibility to trigger Crohn's disease

Harmful gut bacteria co-opt genetic susceptibility to trigger Crohn’s disease

Changes in a single gene open the door for harmful gut bacteria to trigger the inflammation that leads to Crohn’s disease, according to a new study led by Weill Cornell Medicine and NewYork-Presbyterian researchers. These findings could one day help doctors better select targeted treatments for patients with this immune disorder. This particular host gene, …

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Editas Medicine will host a virtual event to highlight initial clinical data from the RUBY trial of EDIT-301 for severe sickle cell disease

Editas Medicine will host a virtual event to highlight initial clinical data from the RUBY trial of EDIT-301 for severe sickle cell disease

Published Medicine, Inc. CAMBRIDGE, Mass., Dec. 01 10, 2022 (GLOBE NEWSWIRE) — Editas Medicine, Inc. (Nasdaq: EDIT), a clinical-stage genome editing company, today announced that it will host a live webinar on Tuesday, December 6, at 8:00 a.m. ET to present initial clinical data from the RUBY Phase 1/2 trial of EDIT-301, being developed for …

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Adding Tumor Lysate-Loaded Autologous Dendritic Cell Vaccination to Standard of Care Associated with Clinically Improved Overall Survival in Patients With Newly Diagnosed and Recurrent Glioblastoma |  Medicine in 2 Minutes

Adding Tumor Lysate-Loaded Autologous Dendritic Cell Vaccination to Standard of Care Associated with Clinically Improved Overall Survival in Patients With Newly Diagnosed and Recurrent Glioblastoma | Medicine in 2 Minutes

1. In this phase 3 non-randomized controlled trial, among 331 patients, patients with newly diagnosed glioblastoma (nGBM) receiving dendritic cell vaccination (DCVax-L) had a median overall survival of 19.3 months versus 16.5 months in outpatient control patients treated with standard of care. 2. Patients with recurrent glioblastoma (rGBM) had a median overall survival of 13.2 …

Adding Tumor Lysate-Loaded Autologous Dendritic Cell Vaccination to Standard of Care Associated with Clinically Improved Overall Survival in Patients With Newly Diagnosed and Recurrent Glioblastoma | Medicine in 2 Minutes Read More »