Invivyd Sets Price for $125 Million Public Offering of Common Stock and Pre-Funded Warrants
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Nov 18 2025
0mins
Should l Buy IVVD?
Source: Newsfilter
Public Offering Announcement: Invivyd, Inc. has priced an underwritten public offering of 44 million shares of common stock at $2.50 per share, along with pre-funded warrants for 6 million shares at $2.4999 each, aiming to raise approximately $125 million before expenses.
Use of Proceeds: The company plans to utilize the net proceeds for commercial preparedness for the potential launch of VYD2311, ongoing research and development for its pipeline programs, and general corporate purposes.
Underwriters and Closing Details: Cantor is the sole book-running manager for the offering, with an option for underwriters to purchase an additional 7.5 million shares. The offering is expected to close around November 19, 2025, pending customary closing conditions.
Company Background: Invivyd is a biopharmaceutical company focused on developing antibodies for serious viral infectious diseases, having received emergency use authorization for a monoclonal antibody in March 2024.
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Analyst Views on IVVD
Wall Street analysts forecast IVVD stock price to rise
4 Analyst Rating
3 Buy
1 Hold
0 Sell
Strong Buy
Current: 1.890
Low
10.00
Averages
10.00
High
10.00
Current: 1.890
Low
10.00
Averages
10.00
High
10.00
About IVVD
Invivyd, Inc. is a biopharmaceutical company. The Company’s proprietary INVYMAB platform approach combines state-of-the-art viral surveillance and predictive modeling with advanced antibody engineering. INVYMAB is designed to facilitate the rapid, serial generation of new monoclonal antibodies (mAbs) to keep pace with evolving viral threats. The Company delivers antibody-based therapies that protect vulnerable people from the devastating consequences of circulating viral threats, such as SARS-CoV-2. Its PEMGARDA (pemivibart) is the Company's first mAb to receive regulatory authorization and is designed to keep pace with SARS-CoV-2 viral evolution. PEMGARDA is used for the pre-exposure prophylaxis (prevention) of COVID-19 in adults and adolescents. Its VYD2311 is optimized for neutralization potency against SARS-CoV-2 lineages such as BA.2.86 and JN.1. The Company also has additional anti-SARS-CoV-2 mAb candidates in discovery and pre-clinical characterization.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- PEMGARDA Revenue Growth: In Q4 2025, PEMGARDA net revenues grew by 31% over Q3 2025 and 25% year-over-year, totaling $53.4 million for the year, demonstrating strong market performance and ongoing commercial expansion for the company.
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- Strong Cash Position: As of December 31, 2025, cash and cash equivalents stood at $226.7 million, bolstered by over $200 million raised in financing during the second half of 2025, ensuring funding for the DECLARATION clinical trial and potential commercialization efforts.
- Clinical Trial Progress: The DECLARATION Phase 3 clinical trial has achieved full enrollment, with FDA granting Fast Track designation for VYD2311, and top-line data expected in mid-2026, showcasing the company's proactive advancements in COVID-19 prevention.
- Management Changes: Distinguished scientist Michael Mina has been appointed Chief Medical Officer, expected to enhance the company's strategic execution in antibody research and market education, further elevating Invivyd's influence in the biopharmaceutical industry.
See More
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- Strong Revenue Expectations: The company anticipates revenue of $51.72 million, representing a 103.8% year-over-year increase, which underscores the growing market demand and acceptance of its COVID-19 therapy products.
- Revision Trends: Over the past three months, EPS estimates have seen one upward revision with no downward adjustments, showcasing analysts' increasing confidence in the company's future performance, while revenue estimates have also experienced one upward revision, reinforcing market optimism about its growth potential.
- FDA Progress: Invivyd recently received FDA agreement on the late-stage trial design for its COVID-19 therapy and was granted fast track status, which will expedite its product launch process and enhance its competitive position in the market.
See More
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- Trial Design: The FDA has requested Invivyd to monitor myocarditis/pericarditis events associated with mRNA COVID-19 vaccines in the LIBERTY trial, a requirement that not only ensures trial safety but may also enhance market acceptance of VYD2311 as a potential preventative option for COVID-19.
- Trial Progress: Invivyd has initiated its registrational Phase 3 trial, DECLARATION, evaluating the efficacy of single or monthly dosing of VYD2311 in preventing symptomatic COVID-19, with topline data from 1,770 participants expected in mid-2026, which will provide crucial evidence for market launch.
- Market Outlook: The development of VYD2311 not only complements existing COVID-19 vaccines but may also offer a new preventative option for younger individuals, and as concerns about vaccine side effects grow, Invivyd's strategic position in the biopharmaceutical market is likely to strengthen.
See More
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- LIBERTY Trial Launch: Invivyd has announced the initiation of the LIBERTY Phase 3 clinical trial, designed to evaluate the safety and immunological profile of VYD2311 compared to mRNA COVID vaccines, with an expected enrollment of 210 participants to explore both standalone and co-administration effects.
- FDA Feedback and Monitoring Requirements: The FDA provided constructive feedback on the LIBERTY trial design and requested specific monitoring for adverse events of special interest related to mRNA vaccines, particularly myocarditis/pericarditis, highlighting concerns for the young adult population to ensure trial safety.
- Background on DECLARATION Trial: The LIBERTY trial builds on the previous DECLARATION trial, which is expected to enroll 1,770 participants to assess the efficacy and safety of VYD2311 in preventing symptomatic COVID, further validating its clinical application potential.
- Antibody Candidate VYD2311: VYD2311 is a novel monoclonal antibody aimed at providing prophylactic and therapeutic options for COVID-19, with pharmacokinetic properties that may allow for effective antibody levels through intramuscular administration, catering to patient-friendly needs.
See More
