Welcome to our dedicated page for Beyond Air news (Ticker: XAIR), a resource for investors and traders seeking the latest updates and insights on Beyond Air stock.
Beyond Air, Inc. develops and commercializes nitric oxide-based medical device and biopharmaceutical programs. Its recurring news centers on LungFit PH, a tankless inhaled nitric oxide system that uses Plasma Pulse Technology to generate nitric oxide from room air, and on commercial access through hospital purchasing channels.
Company updates also cover nitric oxide programs for respiratory indications, including severe lung infections, and Beyond Cancer's ultra-high concentration nitric oxide, or UNO, platform for investigational solid-tumor immunotherapy. Additional recurring themes include clinical data presentations, scientific publications, intellectual property, leadership changes, investor conferences, and governance matters.
Beyond Cancer has appointed Gavin Choy, PharmD as Chief Operating Officer, bringing over 20 years of experience in pharmaceutical and biotechnology sectors. Dr. Choy will oversee clinical trials for ultra-high concentration nitric oxide (UNO), aimed at treating solid tumors. His prior successes include leading clinical development for multiple drug applications across various countries. Beyond Cancer focuses on innovative therapies to enhance treatment options for oncology patients. The company’s UNO therapy has shown potential in preclinical studies to prevent relapse and reduce tumor metastases.
Beyond Cancer, Ltd., an affiliate of Beyond Air (NASDAQ: XAIR), has entered a sponsored research agreement with Stanford School of Medicine to advance its ultra-high concentration nitric oxide (UNO) therapy for solid tumors. Dr. Frederick M. Dirbas and Dr. Mark D. Pegram have been appointed to the Scientific Advisory Board (SAB), with Dirbas serving as Chair. This collaboration aims to influence clinical development and regulatory submissions for UNO therapy, which is being studied for its potential to enhance cancer treatment efficacy and safety. The first human study for UNO is underway, focusing on solid tumors.
Beyond Air, a medical device and biopharmaceutical company, will report its financial results for the third fiscal quarter ending December 31, 2022, on February 9, 2023. The announcement comes as the company focuses on developing inhaled nitric oxide for treating respiratory conditions and ultra-high concentration nitric oxide for solid tumors through its affiliate, Beyond Cancer. A conference call will be held at 4:30 PM ET the same day to discuss these results. Beyond Air has received FDA approval for its LungFit PH system, targeting persistent pulmonary hypertension of the newborn, and is advancing other clinical trials.
Beyond Cancer, an affiliate of Beyond Air (NASDAQ: XAIR), published pre-clinical data showing that ultra-high concentrations of nitric oxide (UNO) significantly enhance immune responses against solid tumors. The study indicated that UNO-treated mice exhibited improved survival rates and reduced tumor metastasis. These findings were detailed in the journal Cancer Cell International. The research supports the potential of UNO as an innovative treatment for solid tumors, with a first-in-human Phase 1 trial already in progress.
Beyond Air, Inc. (NASDAQ: XAIR) announced that Steve Lisi, its Chairman and CEO, will present at the Piper 34th Annual Healthcare Conference from November 29 to December 1, 2022, in New York, NY. Lisi's presentation is scheduled for November 30, 2022, from 1:10 – 1:30 PM ET. Beyond Air specializes in developing inhaled nitric oxide for respiratory conditions and ultra-high concentration nitric oxide for solid tumors. The company has FDA approval for its LungFit PH system aimed at treating persistent pulmonary hypertension in newborns.
Beyond Cancer, Ltd., a subsidiary of Beyond Air (NASDAQ: XAIR), announced promising in vivo data demonstrating that their ultra-high concentration nitric oxide (UNO) therapy combined with anti-PD-1 treatment significantly improves tumor regression rates and survival in CT26 tumor-bearing mice. This data, presented at the 37th Annual SITC Meeting in Boston, highlights the potential of UNO therapy not only to treat primary tumors but also to address metastatic disease effectively. The findings suggest a strong rationale for further advancing clinical studies in combination with immune checkpoint therapies.
Beyond Air reported its financial results for the fiscal quarter ending September 30, 2022, highlighting a net loss of $12.8 million, or ($0.40) per share. This marks an increase in loss compared to $8.7 million, or ($0.36) per share, in the same quarter last year. R&D expenses rose to $4.5 million, up from $2.8 million, driven by spending on ultra-high concentration nitric oxide (UNO). Despite a total cash burn of $10.4 million, the company has $72.5 million in cash and securities. Beyond Air is advancing its LungFit PH commercial launch and plans further studies in various respiratory conditions.
Beyond Air, Inc. (NASDAQ: XAIR) announced positive results from its LungFit PRO pilot study for treating Viral Community-Acquired Pneumonia (VCAP) with inhaled nitric oxide (NO). The study demonstrated a statistically significant reduction in the duration of oxygen support for patients treated with 150 ppm NO compared to standard supportive treatment. Safety data indicated no treatment-related adverse events. These findings support the efficacy and safety of high-concentration NO in pneumonia treatment, particularly for COVID-19 patients, and highlight Beyond Air's commitment to advancing this therapy.
Beyond Air (NASDAQ: XAIR) will report its second fiscal quarter financial results for the period ending September 30, 2022, on November 8, 2022, at 4:30 PM ET. The company focuses on developing inhaled nitric oxide for respiratory conditions and has received FDA approval for its LungFit PH system. This conference call will provide insights into the company’s financial performance and future developments.
Beyond Air (NASDAQ: XAIR) announced positive results from its pilot study of the LungFit GO device for treating severe nontuberculous mycobacteria (NTM) lung disease. Conducted with 15 patients, the study demonstrated favorable safety and efficacy, with no dose reductions required during at-home use. Patients maintained high compliance (>90%) and experienced improvements in quality of life. No serious adverse events were reported, and trends indicated a reduction in bacterial load. This study supports the development of intermittent high-dose nitric oxide therapy for NTM.