Welcome to our dedicated page for Equillium news (Ticker: EQ), a resource for investors and traders seeking the latest updates and insights on Equillium stock.
Equillium Inc. (EQ) is a clinical-stage biotechnology company pioneering therapies for severe autoimmune and inflammatory disorders. This news hub provides investors and stakeholders with timely updates on EQ's scientific advancements, regulatory milestones, and corporate developments.
Access curated press releases and analysis covering key areas including clinical trial results, regulatory communications, research partnerships, and financial performance updates. Our repository simplifies tracking of EQ's novel therapeutic candidates like itolizumab (anti-CD6) and cytokine inhibitors in development.
Bookmark this page for streamlined monitoring of Equillium's progress in addressing conditions such as graft-versus-host disease and lupus nephritis through immunomodulatory approaches. Return regularly for verified updates directly from company filings and authorized sources.
Equillium, Inc. (Nasdaq: EQ) announced interim data from the EQUATE clinical trial, showcasing the efficacy of itolizumab as a first-line treatment for acute graft-versus-host disease (aGVHD). Presented by Dr. John Koreth, the findings revealed a remarkable 100% overall response rate in higher dose cohorts, alongside a significant reduction in corticosteroid use by 40-80%. The trial demonstrated itolizumab's safety profile and its mechanism of action, with sustained clinical responses through Day 57. The company anticipates topline results later this year.
Equillium, Inc. (Nasdaq: EQ) appointed Dr. Y. Katherine Xu to its board of directors, effective February 4, 2021. A partner at Decheng Capital, Dr. Xu brings extensive experience in biotechnology and finance. Her expertise is expected to enhance Equillium’s strategic direction as the company advances into later-stage development of itolizumab, aimed at treating severe autoimmune disorders. Dr. Xu noted the significance of targeting the CD6-ALCAM pathway, particularly after promising interim results for treating acute graft-versus-host disease.
Equillium, Inc. (Nasdaq: EQ) has successfully closed a registered direct offering, raising approximately $30 million in gross proceeds. The offering included 4,285,710 units, with each unit comprising one share of common stock and a warrant for an additional 0.3 shares, priced at $7.00 per unit. The exercise price of the warrants is set at $14.00 per share. Proceeds from this offering will primarily fund the development of the itolizumab pipeline, potential acquisitions, and general corporate purposes.
Equillium, Inc. (Nasdaq: EQ) announced a securities purchase agreement to sell 4,285,710 units at $7.00 each, raising approximately $30 million. Each unit consists of one share of common stock and a warrant for 0.3 additional shares at an exercise price of $14.00. The funds will be used for developing the itolizumab pipeline, acquiring new products, and general corporate needs. The offering closes on February 5, 2021. This offering is registered under a shelf registration statement with the SEC.
Equillium, Inc. (Nasdaq: EQ) announced that interim data from its Phase 1b/2 EQUATE study of itolizumab for acute graft-versus-host disease (aGVHD) will be presented as a late-breaking oral session at the 2021 TCT Meetings, scheduled for February 12, 2021. The study, led by John Koreth, aims to demonstrate the safety and efficacy of itolizumab, a first-in-class monoclonal antibody that targets the CD6-ALCAM pathway, important in T cell activity related to autoimmune disorders. Equillium is focused on treating severe autoimmune and inflammatory conditions with high unmet medical needs.
Equillium, a clinical-stage biotechnology company, announced that its CEO Bruce Steel will present at the H.C. Wainwright Virtual BioConnect Conference on January 11, 2021, at 6:00 am EST. This presentation will focus on itolizumab, a treatment for severe autoimmune and inflammatory disorders. A webcast of the presentation will be accessible on the company’s website under the “Investors” section for 30 days following the event.
Equillium is dedicated to addressing high unmet medical needs in severe immuno-inflammatory diseases.
Equillium Strengthens Leadership with New Executive Appointments
Equillium, Inc. has announced key executive appointments, including Dolca Thomas, M.D., as executive vice president of research and development and chief medical officer. Dr. Thomas has extensive experience from Principia Biopharma and Roche. The company also appointed Michael Son, Ph.D., Nelson Lugo, and Michael Moore to key roles. These strategic hires aim to advance the development of itolizumab for severe autoimmune diseases, particularly acute graft versus host disease, with several critical readouts expected in the coming year.
Equillium, Inc. presented significant findings regarding itolizumab at the 2020 American Society of Hematology Annual Meeting. The study highlighted the drug's ability to suppress the activity of CD4 and CD8 T cells in patients with acute graft-versus-host disease (aGVHD). With no approved first-line therapies for aGVHD, itolizumab's mechanism of targeting the CD6-ALCAM pathway shows promise. Early data from the EQUATE Phase 1b study also supports its potential role in combination with steroids for treating aGVHD.
Equillium, Inc. (Nasdaq: EQ) has announced a virtual Investor and Analyst Day on December 4, 2020, from 9:30 a.m. to 12:00 p.m. ET, focusing on its leading drug candidate, itolizumab, a monoclonal antibody for treating severe autoimmune disorders, including aGVHD, lupus, and uncontrolled asthma. Key presentations will feature Dr. John Koreth from Dana-Farber Cancer Institute and the company's executives. Following presentations, there will be a Q&A session. A webcast will be available for 30 days on the company's Investor Relations website.
Equillium has announced it will not proceed with the EQUINOX Phase 3 clinical trial for itolizumab in COVID-19 patients, citing advancements in vaccines and treatments. CEO Bruce Steel emphasized the decision was strategic amidst a changing treatment landscape. Instead, the company will focus on expanding the itolizumab program for acute graft-versus-host disease, lupus, and asthma studies. The next pipeline updates are expected on December 4, coinciding with the Analyst Day.