Invivyd, Inc.
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- Invivyd, Inc. (Nasdaq: IVVD) is a biopharmaceutical company focused on the discovery, development, and commercialization of antibody-based therapies for serious infectious diseases with pandemic potential, beginning with SARS-CoV-2 and expanding into influenza, respiratory syncytial virus (RSV), measles, and other high-need indications; its proprietary INVYMAB platform integrates viral surveillance, predictive modeling, and advanced antibody engineering to generate monoclonal antibodies (mAbs) that outperform natural immunity by anticipating viral evolution. Core products and pipeline candidates include PEMGARDA (pemivibart), an FDA-authorized half-life extended mAb for pre-exposure prophylaxis of COVID-19 in immunocompromised adults and adolescents; VYD2311, an investigational mAb advancing in the Phase 3 REVOLUTION program (including the DECLARATION pivotal trial and LIBERTY head-to-head study versus mRNA vaccines) for COVID-19 prevention and treatment, with FDA IND approval and trial initiation targeted for late 2025; VBY329, a nominated best-in-class RSV mAb candidate for neonatal, infant, and pediatric prevention targeting multiple variants, with IND readiness planned for the second half of 2026; and earlier candidates such as adintrevimab (in Phase 2/3 for COVID-19 prevention/treatment) and preclinical programs for Long COVID via the SPEAR Study Group. Founded in 2020 and headquartered in Waltham, Massachusetts, the company operates primarily in the United States, targeting vulnerable populations including immunocompromised individuals, neonates, and those with post-vaccination syndromes. Recent developments include a $125 million public equity offering priced in November 2025 (comprising common stock and pre-funded warrants) to fund VYD2311 commercialization readiness, RSV/measles R&D, and general purposes following an August 2025 $50 million offering for similar pipeline advancement; nomination of VBY329 for preclinical development in November 2025 signaling platform expansion beyond COVID-19; FDA clearance of the VYD2311 IND with Phase 3 trial guidance in late 2025; and positive in vitro data for PEMGARDA against emerging SARS-CoV-2 variants.
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Invivyd Announces Completion of Enrollment in Upsized DECLARATION Clinical Trial, a Phase 3 Pivotal Study of VYD2311, an Investigational Antibody to Prevent COVID
Invivyd to Participate in Upcoming Investor Events
Invivyd to Participate in Upcoming Investor Events
Invivyd, Inc. (IVVD) Q1 2026 Earnings Call Transcript
Invivyd Q1 Earnings Call Highlights
Invivyd, Inc. (IVVD) Reports Q1 Loss, Lags Revenue Estimates
Invivyd Reports First Quarter 2026 Financial Results and Recent Business Highlights
Invivyd and Collaborators Author New Manuscript Evaluating Early Tolerability of COVID Monoclonal Antibody and Comparing Results to COVID Vaccination
Invivyd to Host First Quarter 2026 Financial Results and Corporate Update Call on May 14, 2026
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Invivyd Announces Chairman Marc Elia to Speak at POLITICO Health Care Summit
Invivyd, Inc. (IVVD) Discusses Progress in REVOLUTION Clinical Program and Advancement of Measles Monoclonal Antibody Candidate Transcript
Invivyd Stock Surges As FDA Alignment Boosts COVID-19 Program
Invivyd Announces REVOLUTION Program Progress and Advancement of Novel, Potential First- and Best-in-Class Measles Monoclonal Antibody Candidate VMS063 for Treatment and Prevention of Measles
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Invivyd, Inc. (NASDAQ:IVVD) Receives $8.00 Consensus Target Price from Brokerages
Invivyd Announces Presentation at the World Vaccine Congress Washington
Invivyd: A Logical Bull Thesis With A Major Catalyst Approaching
Invivyd, Inc. (NASDAQ:IVVD) Receives $8.00 Consensus Target Price from Brokerages