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. (Nasdaq: EQ) is a La Jolla, California–based clinical-stage biotechnology company that publicly describes its focus as developing novel therapies for severe autoimmune and inflammatory disorders. News about Equillium often centers on the progress of its lead candidate EQ504, an investigational aryl hydrocarbon receptor (AhR) modulator, and on corporate actions that support its development strategy.
Readers of this EQ news page can follow company announcements on clinical and preclinical plans for EQ504, including preparations for Phase 1 studies in ulcerative colitis and related gastrointestinal conditions, as well as potential applications in inflammatory lung or pulmonary diseases. Equillium’s press releases also highlight scientific and translational updates, such as key opinion leader events discussing AhR modulation, intestinal inflammation and the unmet medical need in ulcerative colitis.
In addition to pipeline news, Equillium regularly reports on financing transactions like private placements and at-the-market offerings, which it links to funding the development of EQ504 and extending its operating runway. Corporate governance and leadership updates, including changes in board composition, committee membership and senior roles, are disclosed through both SEC filings and news releases.
Another recurring topic in Equillium’s news flow is its cryptocurrency treasury reserve strategy, which the company has described as part of its broader financial and growth objectives. Updates in this area appear alongside information on cash resources, investment policy changes and strategic priorities.
Investors and observers can use this news feed to monitor Equillium’s clinical plans, scientific positioning around AhR modulation, capital-raising activities, Nasdaq listing developments and treasury strategy, all of which shape the company’s path as a clinical-stage biotech focused on immuno-inflammatory diseases.
Equillium, Inc. (Nasdaq: EQ) has successfully completed an End-of-Phase 1 meeting with the FDA for itolizumab, targeting first-line treatment for acute graft-versus-host disease (aGVHD). This outcome paves the way for a pivotal Phase 3 study aimed at supporting a Biologics License Application (BLA). The study is set to begin in Q4 2021 and will compare itolizumab to standard high-dose corticosteroids, with complete response at Day 29 as the primary endpoint. Itolizumab has received FDA fast track and orphan drug designations.
Equillium, Inc. has announced promising topline results from the Phase 1b EQUATE study for its drug, itolizumab, targeting first-line acute graft-versus-host disease (aGVHD). In a cohort of 20 high-risk patients, the study reported a 55% complete response rate and a 70% overall response rate by Day 29. Patients experienced rapid, durable responses, leading to a significant 67% reduction in corticosteroid usage. The FDA has granted itolizumab fast track and orphan drug designations for aGVHD, with plans for pivotal studies ahead.
Equillium, Inc. (Nasdaq: EQ) announced a new assay for measuring CD6 engagement as a pharmacodynamic marker in autoimmune diseases at the CYTO Virtual Interactive Meeting. The assay, highlighted by Stephen Connelly, achieves up to 96% receptor occupancy in fresh T cells, aiding in optimizing dosages for itolizumab, a monoclonal antibody targeting CD6. This development supports ongoing clinical trials for conditions including graft-versus-host disease and lupus. The assay was developed in collaboration with Precision for Medicine.
Equillium, a clinical-stage biotechnology company, announced its participation in the JMP Securities Life Sciences Conference on June 16-17, 2021. CEO Bruce Steel will overview itolizumab’s mechanism and ongoing clinical programs, focusing on the EQUATE study data for acute graft-versus-host disease, which will be revealed on June 11, 2021, at EHA. Attendees can access a live webcast of the presentation on the company’s website. Equillium develops itolizumab for severe autoimmune and inflammatory disorders, addressing critical medical needs.
Equillium, Inc. (Nasdaq: EQ) announced a collaboration with the Kennedy Institute for Rheumatology and the University of Oxford to study itolizumab, a CD6 monoclonal antibody, for severe autoimmune disorders. This research will investigate how itolizumab influences T cell responses through the CD6-ALCAM pathway, crucial in rheumatic diseases. With less than 25% of rheumatoid arthritis patients achieving remission on standard treatments, this collaboration aims to develop novel therapeutic strategies. The study is expected to enhance the understanding of CD6 biology and improve treatment outcomes.
Equillium, Inc. (Nasdaq: EQ) will host a conference call on June 11, 2021, at 8:00 am ET to discuss topline data from the EQUATE study of itolizumab for treating acute graft-versus-host disease (aGVHD) at EHA2021 Virtual Congress. The conference will feature speakers like Dolca Thomas, M.D., Steve Connelly, Ph.D., and CEO Bruce Steel, followed by a Q&A session. The company emphasizes that the risk-benefit profile supports advancing itolizumab in first-line therapy for severe autoimmune disorders. A live webcast will be accessible on their website.
Equillium, a clinical-stage biotech company, announced its participation in the Jefferies Virtual Healthcare Conference, scheduled for June 1-4, 2021. CEO Bruce Steel and Dr. Dolca Thomas will discuss ongoing clinical programs for itolizumab, targeting severe autoimmune disorders, including acute graft-versus-host disease, lupus/lupus nephritis, and uncontrolled asthma. The presentation is set for June 2 at 11:00 AM ET, accessible via a live webcast on their website, with an archived replay available for 90 days.
Equillium, Inc. (Nasdaq: EQ) announced the presentation of three posters at the 2021 AAI Annual Meeting, showcasing the novel mechanism of action of itolizumab. This first-in-class monoclonal antibody targets the CD6-ALCAM pathway to modulate T cell responses, which are crucial in autoimmune diseases. Key findings include significant reductions in pro-inflammatory cytokine secretion and the development of a pharmacodynamic biomarker assay to monitor CD6 levels in patients. The research underscores the potential of itolizumab in treating conditions like aGVHD and lupus.
Equillium, Inc. (Nasdaq: EQ) reported positive results from its Phase 1b EQUALISE study in systemic lupus erythematosus, showing safety and a dose-dependent reduction in CD6 expression on T cells. The company raised $29.9 million from a direct offering, boosting its cash reserves to $104.1 million, sufficient to fund operations into late 2023. R&D expenses rose to $5.9 million, increasing the net loss to $9.0 million for Q1 2021, compared to $7.8 million last year. Upcoming data catalysts for 2021 include topline results from the EQUATE study and interim data from the EQUALISE study.
Equillium, Inc. (Nasdaq: EQ) announced positive data from its EQUATE study of itolizumab in acute graft-versus-host disease (aGVHD). An abstract detailing these results has been accepted for oral presentation at EHA2021 on June 11, 2021. The study involves 10 patients with Grade III-IV aGVHD and aims to evaluate safety and efficacy. Itolizumab is designed for first-line treatment of aGVHD, a condition with no approved therapies. The observed benefit-risk profile supports further randomized trials to establish its clinical potential.
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