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ARDS
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Arcadis sets mid-single-digit growth target, eyes high-teens margin by 2029
Investing.com -- Dutch engineering and consultancy group Arcadis (AS:ARDS) set targets for mid-single-digit organic revenue growth and long term profitability on Tuesday, while also announcing plans to streamline its portfolio and reduce o…
Pneumonia Market Set to Witness Robust Growth During the Forecast Period (2026-2036), Driven by Advancing Therapeutics and Rising Disease Burden | DelveInsight
The growth of the pneumonia market is expected to be primarily driven by an expanding patient population and advancements in diagnostic methods. Additionally, the expected launch of emerging therapies such as Tosatoxumab (AR-301) (Aridis P…
Looking at the underlying holdings of the ETFs in our coverage universe at ETF Channel, we have compared the trading price of each holding against the average analyst 12-month forward target price, and computed the weighted average implied…
Arcadis price target lowered to €52 by KeyBanc on regional slowdown
Investing.com - KeyBanc has reduced its price target on Arcadis (AS:ARDS) NV (AS:ARCAD) to €52.00 from €55.00 while maintaining an Overweight rating on the engineering and consulting firm’s stock. The adjustment follows virtual meetings be…
Aridis Pharmaceuticals Announces Third Quarter 2023 Financial Results and Business Update
Received two grant awards from the National Institute of Allergy and Infectious Diseases, a division of the National Institutes of Health LOS GATOS, Calif., Nov. 03, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (OTCQB: ARDS), a bi…
Aridis Pharmaceuticals Announces $2 Million Offering
Los Gatos, Calif., Aug. 02, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (OTC: ARDS), a biopharmaceutical company focused on the discovery and development of novel anti-infective therapies for treating life-threatening infections,…
Aridis Receives Agreement from the European Medicines Agency (EMA) on the Clinical Study Design and a Single Confirmatory Phase 3 Study of AR-301
LOS GATOS, Calif., July 17, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) today announced positive feedback from the European Medicines Agency (EMA) on the Company’s proposed single confirmatory Phase 3 study of inve…
Aridis’ AR-301 Monoclonal Antibody is Among the First Biologics to Receive FDA’s Qualified Infectious Diseases Product (QIDP) Designation
QIDP designation for Biologics provides FDA Priority Review status LOS GATOS, Calif., July 12, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS), a biopharmaceutical company focused on the discovery and development of no…
Aridis Pharmaceuticals' AR-301 Eligible for Consideration under FDA’s Limited Population Pathway for Antibacterial and Antifungal Drugs (LPAD)
LPAD may provide alternative pathways for streamlined product approval LOS GATOS, Calif., June 20, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS), a biopharmaceutical company focused on the discovery and development o…
Aridis Pharmaceuticals Announces First Quarter 2023 Financial Results and Business Update
LOS GATOS, Calif., June 08, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS), a biopharmaceutical company focused on the discovery and development of novel anti-infective therapies for treating life-threatening infectio…
Aridis Receives Agreement from the FDA on a Single Confirmatory Phase 3 Study of AR-301 and the Clinical Study Design
LOS GATOS, Calif., May 31, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) today announced positive feedback from the FDA on the Company’s proposed single confirmatory Phase 3 study of investigational monoclonal antibo…
Aridis Pharmaceuticals Receives Nasdaq Notice on Late Filing of its Form 10-Q
LOS GATOS, Calif., May 25, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) (“Aridis” or the “Company”), a biopharmaceutical company, announced today that it received a notice (the “Notice”) from the Listing Qualificati…
Aridis Pharmaceuticals Receives Nasdaq Notice on Late Filing of its Form 10-K
LOS GATOS, Calif., April 26, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) (“Aridis” or the “Company”), a biopharmaceutical company, announced today that it received a notice (the “Notice”) from the Listing Qualifica…
LOS GATOS, Calif., March 31, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) (“Aridis” or the “Company”), a biopharmaceutical company, today announced a corporate update on recent developments. The Company received wri…
Aridis Pharmaceuticals Announces $2.28 Million Registered Direct Offering of Common Stock
Los Gatos, Calif., March 14, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS), a biopharmaceutical company, today announced that it has entered into a definitive agreement for the issuance and sale of an aggregate of 6,…
Aridis Meets Primary and Secondary Endpoints in Phase 2a Study of AR-501 in Cystic Fibrosis Patients
The study achieved high uptake of AR-501 in the respiratory tract at levels that were more than 50-fold higher than required for inhibition of the target bacteria P. aeruginosa LOS GATOS, Calif., March 13, 2023 (GLOBE NEWSWIRE) -- Aridis P…
In virtuous cycle, foundation uses drug royalty riches to back new cystic fibrosis drug research in Bay Area
The Cystic Fibrosis Foundation is spinning some of the half-billion dollars it received as part of a royalty deal in 2016 into Bay Area companies looking at ways to tackle persistent infections and perhaps even mutation-fixing cures. Conti…
Aridis Reports Top-Line Results of the Phase 3 Double-Blinded, Superiority Trial of AR-301 For the Treatment of Staphylococcus aureus Ventilator Associated Pneumonia (VAP)
LOS GATOS, Calif, Jan. 25, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS) today announced top-line results from the AR-301-002 Phase 3 study, which evaluated the superiority of adjunctive use of the investigational mo…
New Approaches to Treating Infections in Cystic Fibrosis Patients - AR 501 Phase 2 Trial Update
AR-501 is an inhaled formulation of gallium citrate with broad-spectrum anti-infective activity being developed to treat chronic lung infections in CF patients Los Gatos, Calif., Jan. 17, 2023 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, In…
Aridis Pharmaceuticals to Discuss Topline Data from Phase 3 Study of AR-301 During Corporate Update Call on January 25
Los Gatos, Calif., Dec. 28, 2022 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (NASDAQ: ARDS), a biopharmaceutical company focused on the discovery and development of novel anti-infective therapies to treat life-threatening infections,…
(Updated) Aridis Pharmaceuticals Receives Equity Investment from the Cystic Fibrosis Foundation
Los Gatos, Calif., Dec. 12, 2022 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (NASDAQ: ARDS), a biopharmaceutical company today announced the Cystic Fibrosis Foundation invested $4.85 million in Aridis common stock on market terms unde…
Aridis Pharmaceuticals Receives Equity Investment from the Cystic Fibrosis Foundation
Los Gatos, Calif., Dec. 12, 2022 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (NASDAQ: ARDS), a biopharmaceutical company today announced the Cystic Fibrosis Foundation invested $4.85 million in Aridis common stock on market terms unde…
Aridis Signs Exclusive Terms to Secure Worldwide Commercial Licenses for Pan-Ebola and Pan-Marburg Monoclonal Antibody Programs from Mapp Biopharmaceutical
The Sudan Ebola and Marburg mAb programs were awarded approximately $190 million of BARDA funding covering manufacturing, efficacy and safety evaluations, and regulatory approval Los Gatos, Calif., Dec. 05, 2022 (GLOBE NEWSWIRE) -- Aridis…
Aridis Announces a Key Milestone of Closing of Patient Enrollment in the Phase 2a Study of AR-501 in Cystic Fibrosis Patients
Los Gatos, Calif., Nov. 30, 2022 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (NASDAQ: ARDS), a biopharmaceutical company focused on the discovery and development of novel anti-infective therapies for treating life-threatening infectio…
Aridis to Participate in Key Opinion Leader Discussion on Immunotherapy for Infectious Diseases
The Company’s superiority Phase 3 ‘ASAP-1' study of AR-301 monoclonal antibody in S. aureus pneumonia and the pending data readoutwill be a focus of the KOL event Los Gatos, Calif., Nov. 22, 2022 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals,…
Aridis Pharmaceuticals Announces Third Quarter 2022 Financial Results and Business Update
Top-line data from the Phase 3 clinical trial evaluating AR-301 for the treatment of VAP expected in December of this year LOS GATOS, Calif., Nov. 21, 2022 (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (Nasdaq: ARDS), a biopharmaceutica…
DICE Therapeutics (DICE) Up on Top-Line Data From Psoriasis Study
DICE Therapeutics DICE skyrocketed 62.27% on Oct 11 after the company announced positive top-line data from a phase I study evaluating its lead therapeutic candidate, DC-806, for treating psoriasis. Shares of DICE Therapeutics have surged…
scPharmaceuticals (SCPH) Plunges Despite Furoscix's FDA Approval
scPharmaceuticals SCPH recently announced that the FDA approved its proprietary formulation of furosemide in 80 mg dosage delivered via an on-body infusor, marketed under the trade name Furoscix (furosemide injection) for treating congesti…
Iovance (IOVA) Doses First Patient in TIL Cancer Therapy Study
Iovance Biotherapeutics IOVA recently announced that the first patient had been dosed in phase I/II IOV-GM1-201 study, evaluating the company’s genetically modified, tumor-infiltrating lymphocyte (TIL) therapy, IOV-4001 in patients with pr…
Wave Therapeutics (WVE) Up on Update From Huntington's Study
Shares of Wave Lifesciences WVE were up 8.26% on Sep 20, after the company announced a positive update from its ongoing phase Ib/IIa SELECT-HD study on its clinical candidate, WVE-009 for treating Huntington’s disease (HD). Wave Therapeuti…
Intellia (NTLA) Reports Positive Results for CRISPR Candidates
Intellia Therapeutics NTLA and its partner Regeneron Pharmaceuticals REGN recently announced positive interim results from an ongoing phase I study of its lead candidate NTLA-2001. The candidate is being developed as a single-dose treatmen…
bluebird's (BLUE) Gene Therapy Gets FDA Nod for CALD
bluebird bio BLUE recently received accelerated FDA approval for Syskona (elivaldogene autotemcel), also known as eli-cel, as a treatment for patients less than 18 years of age with early, active cerebral adrenoleukodystrophy (CALD). Upon…
Pfizer (PFE) Seeks FDA Nod for Its Oral Antiviral COVID Pill
Pfizer PFE announced that it had submitted a new drug application (“NDA”) to the FDA seeking approval for an oral antiviral pill for COVID-19, Paxlovid (nirmatrelvir [PF-07321332] tablets and ritonavir tablets). The NDA seeks approval for…
Why Endo (ENDP) Stock Wilted After its Surge on Tuesday?
Shares of Endo International Plc ENDP crashed 26% on Jun 29, right after the pharma stock witnessed a surge the day before. Endo is knee-deep in trouble with several litigation suits over opioid sales that have caused shares to underperfor…
Today’s Biggest Pre-Market Stock Movers: 10 Top Gainers and Losers on Wednesday
Good morning, investor! We’ve reached the halfway point of the week and we’re starting it with an overview of the biggest pre-market stock movers for Wednesday! A close-up shot of the Wall Street street sign representing Pre-Market Stock M…
Carnival (NYSE:CCL) stock is sailing higher on Tuesday and there’s several reasons why that investors need to know about. Carnival (CCL stock) cruise ship on water in front of beach with chairs Source: Flickr Let’s dive into all the news b…