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Invivyd

Full company profile

uuid00000n6

Namestring
Invivyd
Legal namestring
Invivyd, Inc.
Websiteurl
invivyd.com
Company typeenum
Public
Founded yearint
2020
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersWaltham, United States
HQ citystring
Waltham
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
monoclonal antibody therapy, infectious disease treatment, COVID-19 prophylaxis, viral immunology platform, antibody engineering
Industry1 code
1Monoclonal Antibody Therapeutics (mAbs)
CodeHLAAAAAAPrimaryYes
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Monoclonal Antibody Therapeutics
Social media profiles3 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1PEMGARDA Product Sales
TypeOne Time License
Description

Net product revenue from sales of PEMGARDA (pemivibart), a monoclonal antibody authorized for emergency use in COVID-19 pre-exposure prophylaxis, marketed primarily to immunocompromised patients who do not respond well to vaccines

globenewswire.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Marketing or Sales, Operations
Pricing details1 tier
1PEMGARDA (pemivibart) for COVID-19 pre-exposure prophylaxis
ModelOtherBilling cadenceOther
Notes

Distributed under Emergency Use Authorization; patient support program Invivyd Care provides benefits investigations, access and reimbursement assistance, treatment coordination, and payor advocacy

biospace.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Invivyd is a clinical-stage and commercial biopharmaceutical company that discovers, develops, and commercializes monoclonal antibody (mAb) therapies for serious viral infectious diseases. Its commercial product, PEMGARDA (pemivibart), is authorized under FDA Emergency Use Authorization for COVID-19 pre-exposure prophylaxis in immunocompromised adults and adolescents. The company also advances a pipeline of monoclonal antibody candidates (VYD2311 for COVID-19 prevention/treatment and Long COVID, VBY329 for RSV, VMS063 for measles) generated through its proprietary INVYMAB platform that integrates viral surveillance, predictive modeling, deep B-cell mining, and antibody engineering.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • PEMGARDA demonstrated approximately 80% protection against COVID-19 variants in clinical studies versus CDC-estimated 40-50% efficacy for mRNA vaccines in healthy individuals
+2 more records
Product overview1 text field

Invivyd is a biopharmaceutical company with a single commercial product and multiple pipeline candidates. PEMGARDA (pemivibart) is the company's authorized monoclonal antibody for COVID-19 pre-exposure prophylaxis, launched in March 2024. The development pipeline centers on VYD2311 as a next-generation COVID-19 prevention and treatment candidate in Phase 3 trials, with additional indications including Long COVID and a robust expansion pipeline including VBY329 for RSV (prophylaxis in children) and VMS063 for measles, both in development. All candidates leverage the proprietary INVYMAB platform which combines viral surveillance, predictive modeling, antibody discovery through B-cell mining, and antibody engineering for affinity maturation.

Product and service4 records
1PEMGARDA (pemivibart)
CategoryCommercial product
Description

A monoclonal antibody authorized for emergency use in COVID-19 pre-exposure prophylaxis for adults and adolescents (12 years of age and older weighing at least 40 kg) with moderate to severe immune compromise who may not respond adequately to COVID-19 vaccination.

2VYD2311
CategoryPipeline candidate
Description

A next-generation monoclonal antibody candidate designed as a vaccine-alternative antibody for COVID-19 prevention, with additional indications under development including Long COVID treatment and COVID-19 treatment; in Phase 3 LIBERTY pivotal trial with Fast Track designation.

3VBY329 (RSV)
CategoryPipeline candidate
Description

A selected potential best-in-class monoclonal antibody candidate for respiratory syncytial virus (RSV) prophylaxis targeting children, with increased potency and resistance to RSV variants compared to current treatments; targeting IND readiness in 2H 2026.

4VMS063 (Measles)
CategoryPipeline candidate
Description

A novel measles monoclonal antibody candidate targeting the Fusion protein for treatment and prevention of measles; discovered in April 2026 with IND-enabling studies underway and target IND readiness in late 2026.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-05-11
Description

Collaborative research presentation at ESCMID comparing monoclonal antibody side effect data with Sanofi's COMPARE trial results for protein-based COVID vaccines

Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2026-04-08
Description

Olympic gold medalist skier serving as public ambassador for 'Antibodies for Any Body' national education campaign to raise public awareness about antibody-based treatments for disease protection; campaign launched spring 2026 with digital platform and wellness assessment tools

3Jim Harbaugh
Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2025-02-13
Description

NFL head coach partnered with Invivyd for COVID awareness campaign 'Common, Not A Cold' to educate Americans about ongoing COVID-19 impact and antibody treatment options

stocktitan.net
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Vir Biotechnology develops monoclonal antibodies for serious infectious diseases, including sotrovimab (Xevudy) for COVID-19, and is advancing pipeline candidates for influenza and hepatitis B. It is the most direct peer to Invivyd in terms of mAb-based infectious disease strategy and target indications.

TypeBroad incumbent
Description

AstraZeneca developed Evusheld (tixagevimab/cilgavimab), a long-acting monoclonal antibody combination for COVID-19 pre-exposure prophylaxis, directly competing with PEMGARDA in the immunocompromised patient segment. As a large-cap incumbent, AstraZeneca operates a much broader portfolio and has greater commercial reach.

TypeOthers
Description

Regeneron developed the REGEN-COV (casirivimab/imdevimab) monoclonal antibody cocktail for COVID-19 prevention and treatment. As a large-cap biopharmaceutical incumbent, Regeneron has deep antibody discovery capabilities (VelocImmune) and broad therapeutic focus spanning ophthalmology, oncology, and immunology.

TypeBroad incumbent
Description

Eli Lilly developed bebtelovimab, a monoclonal antibody authorized for COVID-19 treatment, and is broadly active in the infectious disease and immunology spaces. As a global pharmaceutical incumbent, Lilly has significantly greater commercial and R&D resources than Invivyd.

TypeEmerging player
Description

Atea Pharmaceuticals is a clinical-stage biopharmaceutical company developing oral antiviral therapies for RNA viruses, including COVID-19 and hepatitis C. While focused on direct-acting antivirals rather than monoclonal antibodies, Atea targets the same viral disease indications and patient populations as Invivyd.

TypeEmerging player
Description

Brii Biosciences developed amubarvimab/romlusevimab, a monoclonal antibody combination for COVID-19, primarily serving the China market. It is comparable to Invivyd as an emerging infectious disease mAb developer, though it operates in a distinct geographic and regulatory environment.

TypeOthers
Description

Adimab is a leading antibody discovery technology company that has historically been an investor in Invivyd (Adagio Therapeutics) and operates in the monoclonal antibody discovery and engineering space. It is a potential platform partner or competitor for antibody discovery capabilities underlying mAb-based infectious disease therapeutics.

TypeOthers
Description

Moderna is a major competitor in COVID-19 prevention through its mRNA vaccines (Spikevax) and is the direct comparator in Invivyd's Phase 3 LIBERTY trial. While operating in a different modality, Moderna competes for the same prevention market and reimbursement dollars as Invivyd's antibody-based approach.

TypeOthers
Description

Pfizer, in partnership with BioNTech, developed Comirnaty, the leading mRNA COVID-19 vaccine, and is a key competitor in the COVID-19 prevention landscape. Pfizer competes with Invivyd for prescriber attention, payer reimbursement, and patient share in both immunocompromised and general populations.

TypeBroad incumbent
Description

Sanofi is a global biopharmaceutical incumbent with a significant vaccines and immunology franchise, including a COVID-19 protein-based vaccine. Invivyd has a scientific collaboration with Sanofi (COMPARE trial), reflecting Sanofi's role as both a potential partner and a competitor in the infectious disease prevention space.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles16 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds6 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors16 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Invivyd

Monoclonal Antibody Therapeuticsinvivyd.com

Invivyd firmographics

Firmographics
Name
Invivyd
Legal name
Invivyd, Inc.
Website
https://invivyd.com
Company type
Public
Founded year
2020
Operating status
Operating
Headcount range
101–250 employees
Ownership category
akta.pro rank

Invivyd industry classification

Industry
Product category
Monoclonal Antibody Therapeutics
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Monoclonal Antibody Therapeutics (mAbs) (HLAAAAAA)

Keywords

  • Monoclonal antibody therapy
  • Infectious disease treatment
  • COVID-19 prophylaxis
  • Viral immunology platform
  • Antibody engineering

Where Invivyd is headquartered

Location

Headquarters

HQ city
Waltham
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Invivyd business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales, Operations

Revenue model

  1. PEMGARDA Product Sales: Net product revenue from sales of PEMGARDA (pemivibart), a monoclonal antibody authorized for emergency use in COVID-19 pre-exposure prophylaxis, marketed primarily to immunocompromised patients who do not respond well to vaccines

Pricing tiers

ModelBillingPrice
OtherOtherPEMGARDA (pemivibart) for COVID-19 pre-exposure prophylaxis

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

Invivyd product offering

Product offering

Core offering

Invivyd is a clinical-stage and commercial biopharmaceutical company that discovers, develops, and commercializes monoclonal antibody (mAb) therapies for serious viral infectious diseases. Its commercial product, PEMGARDA (pemivibart), is authorized under FDA Emergency Use Authorization for COVID-19 pre-exposure prophylaxis in immunocompromised adults and adolescents. The company also advances a pipeline of monoclonal antibody candidates (VYD2311 for COVID-19 prevention/treatment and Long COVID, VBY329 for RSV, VMS063 for measles) generated through its proprietary INVYMAB platform that integrates viral surveillance, predictive modeling, deep B-cell mining, and antibody engineering.

Product overview

Invivyd is a biopharmaceutical company with a single commercial product and multiple pipeline candidates. PEMGARDA (pemivibart) is the company's authorized monoclonal antibody for COVID-19 pre-exposure prophylaxis, launched in March 2024. The development pipeline centers on VYD2311 as a next-generation COVID-19 prevention and treatment candidate in Phase 3 trials, with additional indications including Long COVID and a robust expansion pipeline including VBY329 for RSV (prophylaxis in children) and VMS063 for measles, both in development. All candidates leverage the proprietary INVYMAB platform which combines viral surveillance, predictive modeling, antibody discovery through B-cell mining, and antibody engineering for affinity maturation.

Differentiator

Problem solved

Functional benefit

Products and services

  • PEMGARDA (pemivibart) A monoclonal antibody authorized for emergency use in COVID-19 pre-exposure prophylaxis for adults and adolescents (12 years of age and older weighing at least 40 kg) with moderate to severe immune compromise who may not respond adequately to COVID-19 vaccination.
  • VYD2311 A next-generation monoclonal antibody candidate designed as a vaccine-alternative antibody for COVID-19 prevention, with additional indications under development including Long COVID treatment and COVID-19 treatment; in Phase 3 LIBERTY pivotal trial with Fast Track designation.
  • VBY329 (RSV) A selected potential best-in-class monoclonal antibody candidate for respiratory syncytial virus (RSV) prophylaxis targeting children, with increased potency and resistance to RSV variants compared to current treatments; targeting IND readiness in 2H 2026.
  • VMS063 (Measles) A novel measles monoclonal antibody candidate targeting the Fusion protein for treatment and prevention of measles; discovered in April 2026 with IND-enabling studies underway and target IND readiness in late 2026.

Quantifiable outcome

  • PEMGARDA demonstrated approximately 80% protection against COVID-19 variants in clinical studies versus CDC-estimated 40-50% efficacy for mRNA vaccines in healthy individuals
  • +2 more outcomes

Companies that use Invivyd

Customer profile

Named customers4 records

Segments2 records

Ideal customer profiles1 record

Invivyd technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature3 records

Invivyd partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered minor and core.

  • Sanofi (COMPARE trial collaboration)minorStrategic or Co-development Partner · 11 May 2026Collaborative research presentation at ESCMID comparing monoclonal antibody side effect data with Sanofi's COMPARE trial results for protein-based COVID vaccines
  • Lindsey VonncoreGTM or Marketing Partner · 8 April 2026Olympic gold medalist skier serving as public ambassador for 'Antibodies for Any Body' national education campaign to raise public awareness about antibody-based treatments for disease protection; campaign launched spring 2026 with digital platform and wellness assessment tools
  • Jim HarbaughcoreGTM or Marketing Partner · 13 February 2025NFL head coach partnered with Invivyd for COVID awareness campaign 'Common, Not A Cold' to educate Americans about ongoing COVID-19 impact and antibody treatment options

Scale indicators8 records

Recent moves6 records

Expansion highlights7 records

Invivyd competitors and assessment

Company assessment

Direct peers

  • Vir Biotechnology: Vir Biotechnology develops monoclonal antibodies for serious infectious diseases, including sotrovimab (Xevudy) for COVID-19, and is advancing pipeline candidates for influenza and hepatitis B. It is the most direct peer to Invivyd in terms of mAb-based infectious disease strategy and target indications.

Broad incumbents

  • AstraZeneca: AstraZeneca developed Evusheld (tixagevimab/cilgavimab), a long-acting monoclonal antibody combination for COVID-19 pre-exposure prophylaxis, directly competing with PEMGARDA in the immunocompromised patient segment. As a large-cap incumbent, AstraZeneca operates a much broader portfolio and has greater commercial reach.
  • Eli Lilly: Eli Lilly developed bebtelovimab, a monoclonal antibody authorized for COVID-19 treatment, and is broadly active in the infectious disease and immunology spaces. As a global pharmaceutical incumbent, Lilly has significantly greater commercial and R&D resources than Invivyd.
  • Sanofi: Sanofi is a global biopharmaceutical incumbent with a significant vaccines and immunology franchise, including a COVID-19 protein-based vaccine. Invivyd has a scientific collaboration with Sanofi (COMPARE trial), reflecting Sanofi's role as both a potential partner and a competitor in the infectious disease prevention space.

Others

  • Regeneron Pharmaceuticals: Regeneron developed the REGEN-COV (casirivimab/imdevimab) monoclonal antibody cocktail for COVID-19 prevention and treatment. As a large-cap biopharmaceutical incumbent, Regeneron has deep antibody discovery capabilities (VelocImmune) and broad therapeutic focus spanning ophthalmology, oncology, and immunology.
  • Adimab: Adimab is a leading antibody discovery technology company that has historically been an investor in Invivyd (Adagio Therapeutics) and operates in the monoclonal antibody discovery and engineering space. It is a potential platform partner or competitor for antibody discovery capabilities underlying mAb-based infectious disease therapeutics.
  • Moderna: Moderna is a major competitor in COVID-19 prevention through its mRNA vaccines (Spikevax) and is the direct comparator in Invivyd's Phase 3 LIBERTY trial. While operating in a different modality, Moderna competes for the same prevention market and reimbursement dollars as Invivyd's antibody-based approach.
  • Pfizer: Pfizer, in partnership with BioNTech, developed Comirnaty, the leading mRNA COVID-19 vaccine, and is a key competitor in the COVID-19 prevention landscape. Pfizer competes with Invivyd for prescriber attention, payer reimbursement, and patient share in both immunocompromised and general populations.

Emerging players

  • Atea Pharmaceuticals: Atea Pharmaceuticals is a clinical-stage biopharmaceutical company developing oral antiviral therapies for RNA viruses, including COVID-19 and hepatitis C. While focused on direct-acting antivirals rather than monoclonal antibodies, Atea targets the same viral disease indications and patient populations as Invivyd.
  • Brii Biosciences: Brii Biosciences developed amubarvimab/romlusevimab, a monoclonal antibody combination for COVID-19, primarily serving the China market. It is comparable to Invivyd as an emerging infectious disease mAb developer, though it operates in a distinct geographic and regulatory environment.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

Invivyd social profiles

Digital presence

Invivyd compliance and trust

Trust signal

Compliance1 record

Invivyd financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Invivyd leadership team

Management profile

Number of profiles

Profiles16 records

Invivyd funding detail

Funding detail

Funding overview

Funding rounds6 records

Investors16 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Invivyd M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Invivyd

What does Invivyd do?

Invivyd is a clinical-stage and commercial biopharmaceutical company that discovers, develops, and commercializes monoclonal antibody (mAb) therapies for serious viral infectious diseases. Its commercial product, PEMGARDA (pemivibart), is authorized under FDA Emergency Use Authorization for COVID-19 pre-exposure prophylaxis in immunocompromised adults and adolescents. The company also advances a pipeline of monoclonal antibody candidates (VYD2311 for COVID-19 prevention/treatment and Long COVID, VBY329 for RSV, VMS063 for measles) generated through its proprietary INVYMAB platform that integrates viral surveillance, predictive modeling, deep B-cell mining, and antibody engineering.

Is Invivyd a public or private company?

Invivyd is a public company. It is classified as public and is currently operating.

When was Invivyd founded?

Invivyd was founded in 2020. It employs 101 to 250 people.

Where is Invivyd based?

Invivyd is headquartered in Waltham, United States, in the North America region.

How does Invivyd make money?

One revenue line is on record: PEMGARDA Product Sales.

Who are Invivyd's main competitors?

Vir Biotechnology is listed as a direct peer. Broad incumbents are AstraZeneca, Eli Lilly and Sanofi. Others are Regeneron Pharmaceuticals, Adimab, Moderna and Pfizer. Emerging players are Atea Pharmaceuticals and Brii Biosciences.

Does Invivyd have an API?

No public API is recorded for Invivyd.

What industry is Invivyd in?

Invivyd's product category is Monoclonal Antibody Therapeutics. Its primary akta.pro industry code is HLAAAAAA, Monoclonal Antibody Therapeutics (mAbs). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
Ticker ReportInvivyd’s VYD2311 Phase III Study Meets Safety Goals, Eyes FDA Accelerated ApprovalInvivyd reported Phase III LIBERTY study results for VYD2311, an intramuscular monoclonal antibody, showing a statistically significant safety advantage over an mRNA vaccine. The company plans to seek FDA accelerated approval based on serum neutralizing antibody titers, with further data expected from the DECLARATION study.American Banking and Market NewsInvivyd’s VYD2311 Phase III Study Meets Safety Goals, Eyes FDA Accelerated ApprovalInvivyd reported Phase III LIBERTY study results for VYD2311, an intramuscular monoclonal antibody, showing a statistically significant safety advantage over an mRNA vaccine. The company plans to seek FDA accelerated approval based on serum neutralizing antibody titers, with further data expected from the DECLARATION study.MarketBeatInvivyd’s VYD2311 Phase III Study Meets Safety Goals, Eyes FDA Accelerated ApprovalInvivyd reported topline results from its Phase III LIBERTY study of VYD2311, an intramuscular monoclonal antibody for COVID-19 prevention, which met safety and tolerability goals. The study showed fewer adverse events and injection-site reactions with VYD2311 than with the mRNA vaccine, and the company plans to seek accelerated FDA approval based on neutralizing antibody titers.STATInvivyd's pursuit of a Covid vaccine alternative gets a lift, but an FDA hurdle may awaitInvivyd reported Phase 3 LIBERTY study results showing its antibody VYD2311 had fewer side effects than Pfizer's Comirnaty. After six days, 57% of VYD2311 recipients reported headaches, chills, fatigue, or pain versus 91% for Comirnaty, a statistically significant difference. The study also showed better tolerability at 56 days and safe combination with Comirnaty.Defense WorldCritical Comparison: MiMedx Group (NASDAQ:MDXG) and Invivyd (NASDAQ:IVVD)MiMedx Group beats Invivyd on 11 of 14 factors, including profitability and revenue. MiMedx has higher revenue ($418.63M vs $53.43M) and positive net margins, while Invivyd is loss-making. Analysts favor Invivyd due to higher upside potential.Clinical Trials ArenaInvivyd’s Covid-directed mAb hits Phase III safety goalsInvivyd's VYD2311 met safety and tolerability endpoints in a Phase III study, showing fewer adverse events than Comirnaty. The company delayed topline data from a separate trial, and shares fell after the announcement. It plans to seek FDA accelerated approval pending DECLARATION results.Seeking AlphaInvivyd delays trial data for COVID drug (IVVD:NASDAQ)Invivyd reported positive topline data from its LIBERTY Phase 3 trial for COVID-19 antibody VYD2311, meeting all primary and secondary endpoints. The company now expects to report safety and immunogenicity data from the DECLARATION trial in October, delayed from Q3. Pending positive results, Invivyd plans to seek FDA accelerated approval.Markets DailyComparing MiMedx Group (NASDAQ:MDXG) and Invivyd (NASDAQ:IVVD)MiMedx Group and Invivyd are compared on profitability, institutional ownership, analyst ratings, and valuation. MiMedx beats Invivyd on 11 of 14 factors, with higher revenue and earnings, but Invivyd has a lower P/E ratio and higher upside potential. Analysts favor Invivyd due to its higher probable upside.Hartford Business JournalBiotech company more than triples New Haven HQ spaceInvivyd, a biotech developing infectious disease treatments, signed a long-term lease for about 33,000 square feet in downtown New Haven, more than tripling its headquarters space. The lease includes 17,322 sq ft on the ground floor, 12,563 on the mezzanine, and 2,750 in the basement. The company's CEO Marc Elia was appointed Aug. 30.American Banking and Market NewsInvivyd, Inc. (NASDAQ:IVVD) Receives Average Rating of “Hold” from BrokeragesAnalysts have assigned Invivyd a consensus 'Hold' rating, with an average price target of $8.00. The stock opened at $1.02, and the company missed Q2 earnings estimates with a loss of $0.14 per share. Insiders sold shares, and hedge funds hold a 70.36% stake.