Invivyd, Inc.
NASDAQ Global MarketCapital Structure
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in mil. unless spec.Company Description
- CEO
- Marc William Elia
- Full Time Employees
- 122
- Sector
- Healthcare
- Industry
- Biotechnology
- Address
- 209 Church Street New Haven CT United States of America 06510
- IPO Date
- Aug 6, 2021
- CIK
- 0001832038
- Website
- invivyd.com
- Similar Companies
- Business
- 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.
Company News
Invivyd and the SPEAR Study Group Announce Initiation of “FLINTLOCK” Phase 2 Study of VYD2311, a Monoclonal Antibody for the Potential Treatment of Long COVID or Post-Vaccination Syndrome
Invivyd’s VYD2311 Phase III Study Meets Safety Goals, Eyes FDA Accelerated Approval
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Invivyd's VYD2311 Phase III Study Meets Safety Goals, Eyes FDA Accelerated Approval
Invivyd Outlines Accelerated Approval Submission Path with FDA for COVID-19 Antibody
Invivyd, Inc. (IVVD) Discusses LIBERTY Phase III Topline Data and Next Steps for VYD2311 Regulatory Submission Transcript
Invivyd Announces Positive Topline Results from LIBERTY Phase 3 Study Demonstrating VYD2311 Safety and Tolerability Superior to mRNA-based COVID-19 Vaccine; Announces Regulatory Submission Plans for VYD2311
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Invivyd to Participate in Upcoming September Investor Conferences
BlackRock Inc. Takes $14.08 Million Position in Invivyd, Inc. $IVVD
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Invivyd Appoints Chairman Marc W. Elia as Chief Executive Officer; Approaches Results of VYD2311 studies DECLARATION and LIBERTY
Invivyd, Inc. (IVVD) Reports Q2 Loss, Lags Revenue Estimates
Invivyd Reports Second Quarter 2026 Financial Results and Recent Business Highlights
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Invivyd Announces Receipt of Twelve Months' Advanced Notice of Emergency Use Authorization (EUA) Termination for PEMGARDA® and Provides an Update on Next Steps with the U.S. FDA
Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
NovaBridge Biosciences Appoints Dr. Srishti Gupta as Chief Executive Officer
Invivyd Announces Completion of Enrollment in Phase 3 LIBERTY Trial Evaluating VYD2311 Antibody Versus mRNA COVID-19 Vaccine