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Autoimmune diseases and bone health conditions are not just medical challenges – they’re personal battles that millions of people fight every day. Fortunately, advances in clinical research are providing hope for better treatments and outcomes.
As the biotech sector races to improve the tolerability of these revolutionary treatments, Poolbeg Pharma has a novel solution: an oral therapy, POLB 001, to block the development of CRS, by limiting inflammation without affecting the anti-cancer immuneresponses that are vital for effective immunotherapies.
These CCR8+ Tregs are known to suppress immuneresponses in the tumour microenvironment (TME), allowing cancers to grow unchecked. “DT-7012 This opens the door for a disease-modifying approach both as a monotherapy and in combination, expanding treatment options and offering new hope to millions of patients.”
The designation is reserved for medicines aimed at treating rare diseases that affect fewer than 200,000 people annually in the United States. The company has emphasized that its investigational therapies are designed not only to control symptoms but to alter the course of disease.
The challenge of GPCR drug discovery G protein-coupled receptors (GPCRs) are one of the most desirable and challenging target classes in drug discovery, as their mutation can lead to a wide range of diseases such as cancer, cardiovascular disorders and neurological conditions.
The $400,000 prize, to be shared among the four winners, recognizes their role in creating and advancing a technology that has reshaped how physicians treat leukemia, lymphoma, and multiple myeloma, and is now showing promise in treating autoimmune and infectious diseases. In the early 2000s, both teams began preparing for clinicaltrials.
Nonclinical safety assessment serves as a cornerstone in drug development, providing essential data to identify early signs of potential toxicity and inform subsequent clinicaltrial design. One important aspect of toxicity studies is determining whether the drug produces undesired immune effects.
With an extensive background in these fields, Ichim is dedicated to advancing personalised cellular therapies aimed at addressing age-related diseases, with a special focus on cancer and liver failure. We plan to take SenoVax on a very accelerated pathway and hope to begin clinicaltrials for SenoVax this year, he shares.
Effective immediately, Roche is halting the administration of Elevidys to non-ambulatory DMD patients in both commercial and clinicaltrial settings. ” Duchenne muscular dystrophy is a rare, X-linked, degenerative muscle disease predominantly affecting boys.
Gray, in London to discuss the significance of her recovery at the Third International Summit on Human Genome Editing , described Casgevy as “a new beginning for people with sickle cell disease.” ” Despite its association with genome editing, 1 CRISPR didn’t start out as a tool for fighting genetic disease.
Physicians working in the early 20th century had little choice but to treat the world’s most rampant infectious disease with methods such as these. But even now, more than a century later, TB remains the deadliest infectious disease on Earth, killing about 1.2 million people every year. Subscribe to Asimov Press. tuberculosis.
GSK Licenses Shigella Vaccine Candidate to Bharat Biotech in Push for Global Health Equity GSK today announced a significant step forward in the battle against Shigella a leading cause of diarrhoeal disease and death in children under five by licensing its Shigella vaccine candidate, altSonflex1-2-3 , to Bharat Biotech International Limited (BBIL).
Related news Single-cell analysis of Crohn’s disease reveals a detailed picture of inflammation in the gut Up to half of patients with Crohn’s disease, an inflammatory bowel disease, develop a complication called fibrosis, where the gut becomes scarred and obstructed, causing pain and bloating.
Autoimmune diseases and bone health conditions are not just medical challenges – they’re personal battles that millions of people fight every day. Fortunately, advances in clinical research are providing hope for better treatments and outcomes.
Tests, in mice, of a drug developed by the researchers showed that regulatory T cells can be attracted to specific body parts, boosted in number, and activated to suppress immuneresponse and rebuild tissue. Clinicaltrials in humans are now planned.
Pharmacologic intervention has the opportunity to impact disease progression in the SARS-CoV-2 / COVID-19 crisis. Repurposing of approved therapies is the fastest way to impact patients today, as these medicines have regulatory approval to enable investigator-initiated trials and have a manufacturing process to ensure drug supply.
Additionally, ADSCs possess immunomodulatory properties, enabling them to modulate immuneresponses and promote tissue healing. These characteristics position ADSCs as promising candidates for addressing a wide range of medical conditions, from degenerative diseases to traumatic injuries.
Better activation of innate and adaptive immuneresponses was achieved with CV2CoV, resulting in faster response onset, higher titers of antibodies, and stronger memory B and T cell activation as compared to the first-generation candidate, CVnCoV. “In Induction of innate immunity was investigated via specific cytokine markers.
functions to reset the immune system and potentially provide remission for allergic diseases? 1104 acts upstream in the inflammatory response, targeting one of the first key players: antigen-presenting cells (APCs). In allergic diseases, APCs identify and present unknown antigens to the immune system.
Sanofi and Translate Bio initiate Phase 1 clinicaltrial of mRNA influenza vaccine. Th e first clinicaltrial of a seasonal mRNA flu vaccine candidate is an exciting milestone in our quest for the next generation of inf lu enza vaccines. JUNE 22 , 2021.
In the context of a substantial amount of COVID-19-related research and the launch of numerous clinicaltrials, the French government created this steering committee to prioritize and accelerate high potential clinicaltrials. PARIS–( BUSINESS WIRE )– Inotrem S.A., Sébastien Gibot and Dr. Marc Derive.
Clinicaltrial to assess safety, immuneresponse and reactogenicity, after preclinical data showed high neutralizing antibody levels. The Companies expect interim results from this trial in the third quarter of 2021. About the Phase 1/2 clinicaltrial.
Canadian biopharmaceutical company Medicago has announced that its investigational COVID-19 vaccine generated “significant antibody and cellular immuneresponses” after two doses in all subjects in an early-stage clinicaltrial. Martin Berman-Gorvine. Source link.
Johnson & Johnson Posts Interim Results from Phase 1/2a ClinicalTrial of its Janssen COVID-19 Vaccine Candidate. Johnson & Johnson Posts Interim Results from Phase 1/2a ClinicalTrial of its Janssen COVID-19 Vaccine Candidate. Immuneresponses were similar across the age groups studied, including older adults.
In recognition of this groundbreaking advancement, the 2023 Nobel Prize in Medicine was awarded to Katalin Karikó and Drew Weissman for their pioneering work on mRNA modifications that enabled its clinical use. However, mRNA technology is not limited to infectious diseases.
Blockade of the cluster of differentiation 40 (CD40)-CD40L interaction has potential for treating autoimmune diseases and preventing graft rejection. Antidrug antibodies to KPL-404 were suppressed for 57 days with 10 mg/kg IV and for 50 days with 5 mg/kg SC, further confirming prolonged target engagement and pharmacodynamics.
Adjuvanted S-Trimer COVID-19 vaccine candidates demonstrated favorable safety and tolerability profiles and strong neutralizing immuneresponses in a phase 1 trial.
The phase 1 clinicaltrial was a randomized, double-blind and placebo-controlled study in 150 adult and elderly participants.
Johnson & Johnson (the Company) has begun vaccinating adolescent participants in the ongoing Phase 2a clinicaltrial for its COVID-19 vaccine candidate, developed by the Janssen Pharmaceutical Companies of Johnson & Johnson. Vice Chairman of the Executive Committee and Chief Scientific Officer at Johnson & Johnson.
Adjuvanted recombinant COVID-19 vaccine candidate triggered strong neutralizing antibody responses in all adult age groups. High immuneresponse after a single dose in patients with prior infection shows strong booster potential. For media and investors only. Issued: London UK. About the Phase 2 study.
NK cells are among the front line of protection from infected and abnormal cells as part of the ‘innate immuneresponse’. They recognise ‘cell stress molecules’ on the surface of infected, old, injured and cancerous cells without the need for complex pre-stimulation signals of the adaptive immune system (eg, T cells).
Last week DNA Science covered a setback in a clinicaltrial of a gene therapy for Duchenne muscular dystrophy (DMD). Also recently, FDA’s Cellular, Tissue, and Gene Therapies Advisory Committe turned down a stem cell treatment for amyotrophic lateral sclerosis, aka ALS, Lou Gehrig’s disease, or motor neuron disease.
A healthy immune system defends the body against disease and other conditions. However, if the immune system malfunctions, it can attack healthy cells, tissues and organs. Autoimmune disease impacts different parts of the body, weakening functionality. Autoimmune diseases affect more than 24 million people in the U.S.
NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced positive results from a Phase 2/3 clinicaltrial evaluating the safety, tolerability and immunogenicity of a 10-µg booster (third) dose of the Pfizer-BioNTech COVID-19 vaccine in healthy children 5 through 11 years of age. About the Phase 1/2/3 Trial in Children.
Targeting 4-1BB remained of interest to the immuno-oncology field as cell culture experiments and tumor models in mice suggested that robust anti-tumor immuneresponses could be triggered by anti-4-1BB antibody therapies. This is the T cell type most closely associated with anti-tumor immuneresponses.
NK cells are among the front line of protection from infected and abnormal cells as part of the ‘innate immuneresponse’. They recognise ‘cell stress molecules’ on the surface of infected, old, injured and cancerous cells without the need for complex pre-stimulation signals of the adaptive immune system (eg, T cells).
Advances in disease understanding and combination strategies in haematology We now know that blood cancers are characterised by molecular and phenotypic heterogeneity. Ultimately, novel early detection methods will need to detect cancer cells before they become clinically visible by imaging studies, and preferably in a premalignant state.
a private clinical stage biopharmaceutical company developing Site Specific Immunomodulators (SSIs), a novel platform of immunotherapies designed to restore innate immune function, is pleased to announce an oversubscribed $8 million financing. VANCOUVER, British Columbia, Dec. 09, 2020 (GLOBE NEWSWIRE) — Qu Biologics Inc. ,
reports that Scentech-Medical received approval from the Shamir Medical Center ( Asaf Harofe ) Review Board ( Helsinki committee) for a new clinicaltrial. As part of the trial, the company is verifying the biomarkers that were mapped after its early clinicaltrials conducted at the Meir Medical Center, in Kfar Saba.
P otential to be a safer and effective alternative to the intravenous immunotherapies currently used for Crohn’s Disease.
Crohn’s Disease Therapeutics Market Size $4.7
Phase1b/2 clinical study to be conducted in the United States and several European countries. Billion by 2025.
and Europe.
Nasdaq: NVAX), a late-stage biotechnology company developing next-generation vaccines for serious infectious diseases, today announced an Advance Purchase Agreement with the government of New Zealand for the purchase of 10.7 GAITHERSBURG, Md., 16, 2020 (GLOBE NEWSWIRE) — Novavax , Inc. About Novavax. Novavax, Inc.?(Nasdaq:
Ben-Moshe told BioSpace that BND-22 differs from traditional immunotherapy in that it can elicit a more total immuneresponse. . “It It is a new immune checkpoint that is expressed on three different immune cells: Macrophages, [Natural Killer] NK cells, and T cells. [It]
In a Phase 2/3 clinicaltrial, the Pfizer-BioNTech COVID-19 Vaccine elicited a strong immuneresponse in this age group Three 3-µg doses had favorable safety profile similar to placebo in young children ages 6 months through 4 years in Phase 2/3 clinicaltrial Pfizer-BioNTech COVID-19 Vaccine now authorized in the U.S.
Strong Th1 cell-mediated immuneresponses were also observed for the vaccine candidates with either adjuvant. Clover intends to initiate a separate pivotal clinicaltrial of the S-Trimer vaccine candidate in combination with Dynavax’s advanced CpG 1018 adjuvant plus alum in the first half of 2021.
Nasdaq: NVAX), a late-stage biotechnology company developing next-generation vaccines for serious infectious diseases, today announced that the U.S. Currently in late-phase clinical development, NVXCoV2373 is a stable, prefusion protein made using Novavax’ nanoparticle technology and includes its proprietary MatrixM adjuvant.
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