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Curevo

Full company profile

uuid0000eke

Namestring
Curevo
Legal namestring
Curevo Inc.
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Curevo Inc. is a clinical-stage biotechnology company founded in May 2018 by South Korea's GC Biopharma as its US vaccine affiliate, headquartered in Bothell, Washington. The company develops a single vaccine candidate, amezosvatein (development code CRV-101), a non-mRNA adjuvanted subunit vaccine targeting the glycoprotein E antigen of the varicella zoster virus. The candidate is applied across two indications: prevention of shingles (herpes zoster) in adults aged 50 and older (lead, Phase 3-ready asset), and prevention of chickenpox (varicella) in immunocompromised children (earlier-stage pipeline). The proprietary SLA-SE adjuvant is a synthetic TLR4 agonist formulated in a stable squalene emulsion, developed at Seattle-based Access to Advanced Health Institute (AAHI) and differentiated from the biologically-derived MPL adjuvant used in GSK's Shingrix. The antigen was licensed from the Mogam Institute for Biomedical Research.

Phase 2 data from an 876-patient head-to-head trial (NCT05304351) demonstrated that amezosvatein's anti-gE antibody response is non-inferior to Shingrix (100% vaccine response rate vs 97.9%) with significantly better tolerability (7.3% vs 33.3% Grade 2/3 reactogenicity at the highest dose, p<0.001), zero confirmed shingles cases across 619 amezosvatein recipients over 18.8 months mean follow-up, and stronger T-cell activation markers. A 640-participant Phase 2 extension in adults over age 70 began enrolling in June 2025 to finalize dose selection ahead of Phase 3.

Curevo is pre-revenue and has been funded entirely through venture capital: a $60 million Series A (February 2022), a $26 million Series A1 (November 2022), and a $110 million Series B (March 2025) led by Medicxi with OrbiMed, HBM Healthcare Investments, Sanofi Ventures, RA Capital Management, Janus Henderson Investors, Adjuvant Capital, and founding investor GC Biopharma. The company entered into a definitive agreement on May 26, 2026 to be acquired by Eli Lilly and Company for up to $1.5 billion in cash (upfront plus milestone payments), subject to customary closing conditions including HSR antitrust review. Under Lilly, global development and commercialization of amezosvatein will be executed through Lilly's infrastructure rather than independently.

Short descriptiontext

Curevo is a clinical-stage biotechnology company developing amezosvatein (CRV-101), a non-mRNA adjuvanted subunit vaccine for shingles in adults aged 50+ and chickenpox in immunocompromised children, using a proprietary synthetic TLR4 agonist adjuvant. Founded in 2018 by GC Biopharma, the Bothell, WA-based company was acquired by Eli Lilly in May 2026 for up to $1.5 billion.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBothell, United States
HQ citystring
Bothell
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
non-mRNA vaccines, adjuvanted subunit vaccines, shingles vaccines, infectious disease biotechnology, clinical-stage vaccine development
Industry5 codes
1Prophylactic Human Vaccines (routine, pediatric, adult)
CodeHLAAAEAAPrimaryYes
2Clinical Development & Regulatory for Vaccines (trials, pharmacovigilance, lot release)
CodeHLAAAEAKPrimaryNo
3Pediatric Vaccines
CodeHLAIAEAAPrimaryNo
4Pandemic Preparedness & Rapid-Response Vaccines
CodeHLAIAEAFPrimaryNo
5Vaccine Quality, Safety & Pharmacovigilance
CodeHLAIAEALPrimaryNo
NAICS code1 code
  • Medical and Diagnostic Laboratories62151
SIC code1 code
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Infectious Disease Vaccines
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Acquisition / Liquidity Event
TypeLicensing Royalties
Description

Pre-revenue clinical-stage biotech; primary exit/liquidity event is the May 2026 acquisition by Eli Lilly for up to $1.5 billion (inclusive of upfront and milestone payments), structured as upfront cash plus contingent milestone-linked payments. Founding investor GC Biopharma also received proceeds, potential milestone payments, and future royalty income from the transaction.

curevovaccine.com
2Private Equity Financing
TypeTransaction Fee
Description

Pre-revenue operations funded through venture capital rounds: $60M Series A (Feb 2022), $26M Series A1 (Nov 2022), and $110M Series B (Mar 2025) led by Medicxi with OrbiMed, HBM Healthcare Investments, Sanofi Ventures, RA Capital Management, Janus Henderson Investors, Adjuvant Capital, and founding investor GC Biopharma.

curevovaccine.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain
Pricing details1 tier
1Not publicly disclosed — investigational product pre-commercialization
ModelOther
Notes

Pricing not publicly disclosed; amezosvatein is an investigational vaccine in clinical development. The reference market is the current $4+ billion shingles vaccine market.

curevovaccine.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1Amezosvatein
Description

Lead investigational product, a non-mRNA adjuvanted subunit vaccine (also known as CRV-101) for the prevention of shingles (herpes zoster) in adults and chickenpox (varicella) in children, targeting glycoprotein E (gE) with a TLR4 agonist adjuvant.

curevovaccine.com
Core offering1 text field

Curevo is developing amezosvatein (also known by development code CRV-101), a single non-mRNA, adjuvanted subunit vaccine candidate applied to two indications: prevention of shingles (herpes zoster) in adults aged 50 and older, and prevention of chickenpox (varicella) in immunocompromised children. The lead shingles program has completed an 876-patient Phase 2 head-to-head trial versus GSK's Shingrix meeting both primary immunogenicity non-inferiority and safety endpoints, and is Phase 3-ready; the chickenpox program is positioned as a Phase 1 application for immunocompromised pediatric populations.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 8 values shown
  • 7.3% Grade 2/3 reactogenicity events at highest dose vs 33.3% for Shingrix (p<0.001); more than half reduction in side effects
+7 more records
Product overview1 text field

Curevo Vaccine (Curevo Inc.) is a clinical-stage, privately-held biotechnology company based in Bothell, Washington, developing a focused portfolio of a single, non-mRNA adjuvanted subunit vaccine candidate — amezosvatein (development code CRV-101) — applied across two indications: amezosvatein for shingles (herpes zoster) in adults aged 50+ and amezosvatein for chickenpox (varicella) in children, with the shingles program as the lead Phase 3-ready asset and the chickenpox program as an earlier-stage pipeline application targeted at immunocompromised children. Both indications share the same underlying science (recombinant glycoprotein E antigen plus an optimized TLR4 agonist SLA-SE adjuvant) developed to address tolerability and accessibility gaps left by current standard-of-care vaccines such as Shingrix.

Product and service2 records
1Amezosvatein (CRV-101) for Shingles
CategoryInvestigational vaccine - shingles (herpes zoster) prevention
Description

A non-mRNA, adjuvanted subunit vaccine (also known by development code CRV-101) targeting glycoprotein E (gE) on the varicella zoster virus (VZV) for the prevention of shingles (herpes zoster) in adults aged 50 and older. Uses a synthetic TLR4 agonist (SLA) adjuvant formulated as a stable emulsion (SLA-SE) to deliver immune response non-inferior to Shingrix with significantly lower reactogenicity (7.3% Grade 2/3 reactogenicity at highest dose vs 33.3% for Shingrix, p<0.001). Phase 2 data (NCT05304351, 876 patients) met both primary immunogenicity and safety endpoints; a Phase 2 extension in adults over 70 was enrolling in mid-2025 in preparation for Phase 3.

2Amezosvatein for Chickenpox (Varicella)
CategoryInvestigational vaccine - chickenpox (varicella) prevention
Description

Investigational application of amezosvatein for the prevention of chickenpox (varicella) in children, particularly targeting immunocompromised children for whom current live-attenuated virus (LAV) chickenpox vaccines are difficult to administer. As a non-live, adjuvanted subunit vaccine, amezosvatein is positioned to address limitations of existing LAV vaccines for children with cancer, organ transplants, or genetic or acquired immune deficiencies. Phase 1 trial in immunocompromised children is planned.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierFlagship (Acquirer)TypeStrategic or Co-development PartnerAnnounced on2026-05-26
Description

Definitive agreement announced May 26, 2026 for Eli Lilly to acquire Curevo Inc. for up to $1.5 billion in cash (inclusive of upfront and milestone payments), subject to customary closing conditions including Hart-Scott-Rodino antitrust review. Lilly's global development and commercialization capabilities will accelerate and expand amezosvatein's potential. Relationship is Mutual — strategic acquirer providing commercialization capabilities while advancing Curevo's lead asset into Phase 3 and global markets.

Strategic tierStrategic Advisor (M&A)TypeImplementation/ SI/ Consulting PartnerAnnounced on2026-05-26
Description

Acting as one of two financial advisors to Curevo for the sale to Eli Lilly announced May 26, 2026. Relationship is We to Them — Curevo engages Centerview Partners as financial advisor.

Strategic tierStrategic Advisor (M&A)TypeImplementation/ SI/ Consulting PartnerAnnounced on2026-05-26
Description

Acting as one of two financial advisors to Curevo for the sale to Eli Lilly announced May 26, 2026. Relationship is We to Them — Curevo engages J.P. Morgan Securities LLC as financial advisor.

Strategic tierStrategic Advisor (Legal)TypeImplementation/ SI/ Consulting PartnerAnnounced on2026-05-26
Description

Acting as legal advisor to Curevo for the sale to Eli Lilly announced May 26, 2026. Relationship is We to Them — Curevo engages Cooley LLP as legal counsel.

Strategic tierCore (Technology Developer)TypeStrategic or Co-development PartnerAnnounced on2025-03-17
Description

Seattle-based institute where the SLA-SE adjuvant formulation used in amezosvatein was developed. Relationship is Them to Us — AAHI developed the adjuvant technology used in Curevo's lead product.

6Moncef Slaoui (Board Chair)
Strategic tierFlagship (Board Chair)TypeOthersAnnounced on2025-03-17
Description

Former Chief Scientific Advisor to Operation Warp Speed and nearly 30-year veteran of GlaxoSmithKline, Dr. Slaoui joined Curevo as Board Chair concurrent with the $110M Series B financing in March 2025. He was directly involved in GSK's vaccine pipeline leading to the creation of Shingrix, Cervarix, Mosquirix, Rotarix, and Synflorix. Relationship is Them to Us — high-profile individual advisor/chair.

curevovaccine.com
Strategic tierFlagship (Founding Investor And Licensor)TypeStrategic or Co-development PartnerAnnounced on2018-05-18
Description

Founding investor that established Curevo in 2017/2018 as part of its global market entry strategy, holding a 20.3% equity stake. GC Biopharma funded the Mogam Institute for Biomedical Research, which licensed amezosvatein to Curevo. In May 2026, GC Biopharma sold its entire 20.3% stake to Eli Lilly for approximately 459.9 billion won (~$303.92 million), with total Curevo acquisition up to $1.5 billion including milestone payments; GC Biopharma will also receive future royalty income. Relationship is Mutual — both a capital provider and strategic partner licensing the technology.

Strategic tierFlagship (Technology Licensor)TypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2017-01-01
Description

Research institute funded by South Korea's GC Biopharma from which amezosvatein was licensed. Relationship is Them to Us — Mogam is the licensor of the technology that forms Curevo's lead asset.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

GlaxoSmithKline markets Shingrix, the dominant shingles vaccine that Curevo's lead asset amezosvatein is positioned head-to-head against in Phase 2/3 trials. Shingrix is the standard of care Curevo is differentiated against.

TypeEmerging player
Description

Moderna is developing mRNA-based shingles vaccine candidates, representing a direct future competitive threat to Curevo's non-mRNA amezosvatein. Former Moderna CMO Tal Zaks now sits on Curevo's board, illustrating the cross-competition dynamic.

TypeBroad incumbent
Description

Pfizer has a broad vaccine portfolio (Comirnaty partnership with BioNTech, Prevnar, etc.) and is also developing mRNA shingles vaccine candidates. Major incumbent vaccine manufacturer that Curevo will compete with globally.

TypeDirect peer
Description

Clinical-stage vaccine company developing non-mRNA, adjuvanted subunit vaccines with similar technology approach (synthetic conjugates). Also backed by Medicxi, with Moncef Slaoui as Board Chair. Direct peer in next-generation non-mRNA vaccine development.

TypeEmerging player
Description

Clinical-stage biotech developing VBI-2601, an enveloped virus-like particle (eVLP) shingles vaccine candidate. Direct competitor in the next-generation shingles vaccine space with a different technology platform.

TypeDirect peer
Description

Specializes in adjuvant technology (CpG 1018 used in Heplisav-B hepatitis B vaccine) and vaccine development. Comparable to Curevo in being an adjuvant-platform-focused vaccine company with adjuvanted subunit products.

TypeDirect peer
Description

Develops adjuvanted recombinant protein subunit vaccines (Nuvaxovid COVID vaccine, Matrix-M adjuvant). Strong technology parallel to Curevo's adjuvanted subunit approach and represents a peer in non-mRNA vaccine commercialization.

TypeBroad incumbent
Description

Global vaccine business and Sanofi Ventures is a Curevo Series B investor. Sanofi Pasteur develops competing vaccines across multiple infectious disease indications and represents a strategic incumbent with manufacturing and commercial scale.

TypeBroad incumbent
Description

Major incumbent vaccine manufacturer with shingles franchise (Zostavax predecessor) and broad infectious disease pipeline. Merck is a potential global launch partner or acquirer for shingles assets.

TypeEmerging player
Description

Partnered with Pfizer on Comirnaty and developing mRNA-based shingles vaccine candidates. Represents a future competitive threat to amezosvatein if mRNA shingles products reach approval first.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

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

Ideal customer profile3 records

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 maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

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

Investors9 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 →

Curevo

Infectious Disease Vaccinescurevovaccine.com

Curevo is a clinical-stage biotechnology company developing amezosvatein (CRV-101), a non-mRNA adjuvanted subunit vaccine for shingles in adults aged 50+ and chickenpox in immunocompromised children, using a proprietary synthetic TLR4 agonist adjuvant. Founded in 2018 by GC Biopharma, the Bothell, WA-based company was acquired by Eli Lilly in May 2026 for up to $1.5 billion.

What Curevo does

Curevo Inc. is a clinical-stage biotechnology company founded in May 2018 by South Korea's GC Biopharma as its US vaccine affiliate, headquartered in Bothell, Washington. The company develops a single vaccine candidate, amezosvatein (development code CRV-101), a non-mRNA adjuvanted subunit vaccine targeting the glycoprotein E antigen of the varicella zoster virus. The candidate is applied across two indications: prevention of shingles (herpes zoster) in adults aged 50 and older (lead, Phase 3-ready asset), and prevention of chickenpox (varicella) in immunocompromised children (earlier-stage pipeline). The proprietary SLA-SE adjuvant is a synthetic TLR4 agonist formulated in a stable squalene emulsion, developed at Seattle-based Access to Advanced Health Institute (AAHI) and differentiated from the biologically-derived MPL adjuvant used in GSK's Shingrix. The antigen was licensed from the Mogam Institute for Biomedical Research.

Phase 2 data from an 876-patient head-to-head trial (NCT05304351) demonstrated that amezosvatein's anti-gE antibody response is non-inferior to Shingrix (100% vaccine response rate vs 97.9%) with significantly better tolerability (7.3% vs 33.3% Grade 2/3 reactogenicity at the highest dose, p<0.001), zero confirmed shingles cases across 619 amezosvatein recipients over 18.8 months mean follow-up, and stronger T-cell activation markers. A 640-participant Phase 2 extension in adults over age 70 began enrolling in June 2025 to finalize dose selection ahead of Phase 3.

Curevo is pre-revenue and has been funded entirely through venture capital: a $60 million Series A (February 2022), a $26 million Series A1 (November 2022), and a $110 million Series B (March 2025) led by Medicxi with OrbiMed, HBM Healthcare Investments, Sanofi Ventures, RA Capital Management, Janus Henderson Investors, Adjuvant Capital, and founding investor GC Biopharma. The company entered into a definitive agreement on May 26, 2026 to be acquired by Eli Lilly and Company for up to $1.5 billion in cash (upfront plus milestone payments), subject to customary closing conditions including HSR antitrust review. Under Lilly, global development and commercialization of amezosvatein will be executed through Lilly's infrastructure rather than independently.

Curevo firmographics

Firmographics
Name
Curevo
Legal name
Curevo Inc.
Website
https://curevovaccine.com
Company type
Private
Founded year
2018
Operating status
Acquired
Headcount range
11–50 employees
Short description
Curevo is a clinical-stage biotechnology company developing amezosvatein (CRV-101), a non-mRNA adjuvanted subunit vaccine for shingles in adults aged 50+ and chickenpox in immunocompromised children, using a proprietary synthetic TLR4 agonist adjuvant. Founded in 2018 by GC Biopharma, the Bothell, WA-based company was acquired by Eli Lilly in May 2026 for up to $1.5 billion.
Ownership category
akta.pro rank

Curevo industry classification

Industry
Product category
Infectious Disease Vaccines
NAICS
Medical and Diagnostic Laboratories (62151)
SIC
In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Prophylactic Human Vaccines (routine, pediatric, adult) (HLAAAEAA)
akta.pro secondary industries
Clinical Development & Regulatory for Vaccines (trials, pharmacovigilance, lot release) (HLAAAEAK), Pediatric Vaccines (HLAIAEAA), Pandemic Preparedness & Rapid-Response Vaccines (HLAIAEAF), Vaccine Quality, Safety & Pharmacovigilance (HLAIAEAL)

Keywords

  • Non-mRNA vaccines
  • Adjuvanted subunit vaccines
  • Shingles vaccines
  • Infectious disease biotechnology
  • Clinical-stage vaccine development

Where Curevo is headquartered

Location

Headquarters

HQ city
Bothell
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Curevo business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain

Revenue model

  1. Acquisition / Liquidity Event: Pre-revenue clinical-stage biotech; primary exit/liquidity event is the May 2026 acquisition by Eli Lilly for up to $1.5 billion (inclusive of upfront and milestone payments), structured as upfront cash plus contingent milestone-linked payments. Founding investor GC Biopharma also received proceeds, potential milestone payments, and future royalty income from the transaction.
  2. Private Equity Financing: Pre-revenue operations funded through venture capital rounds: $60M Series A (Feb 2022), $26M Series A1 (Nov 2022), and $110M Series B (Mar 2025) led by Medicxi with OrbiMed, HBM Healthcare Investments, Sanofi Ventures, RA Capital Management, Janus Henderson Investors, Adjuvant Capital, and founding investor GC Biopharma.

Pricing tiers

ModelBillingPrice
Other—Not publicly disclosed — investigational product pre-commercialization

Go-to-market motion2 records

Distribution channels3 records

Marketing channels7 records

Curevo product offering

Product offering

Core offering

Curevo is developing amezosvatein (also known by development code CRV-101), a single non-mRNA, adjuvanted subunit vaccine candidate applied to two indications: prevention of shingles (herpes zoster) in adults aged 50 and older, and prevention of chickenpox (varicella) in immunocompromised children. The lead shingles program has completed an 876-patient Phase 2 head-to-head trial versus GSK's Shingrix meeting both primary immunogenicity non-inferiority and safety endpoints, and is Phase 3-ready; the chickenpox program is positioned as a Phase 1 application for immunocompromised pediatric populations.

Product overview

Curevo Vaccine (Curevo Inc.) is a clinical-stage, privately-held biotechnology company based in Bothell, Washington, developing a focused portfolio of a single, non-mRNA adjuvanted subunit vaccine candidate — amezosvatein (development code CRV-101) — applied across two indications: amezosvatein for shingles (herpes zoster) in adults aged 50+ and amezosvatein for chickenpox (varicella) in children, with the shingles program as the lead Phase 3-ready asset and the chickenpox program as an earlier-stage pipeline application targeted at immunocompromised children. Both indications share the same underlying science (recombinant glycoprotein E antigen plus an optimized TLR4 agonist SLA-SE adjuvant) developed to address tolerability and accessibility gaps left by current standard-of-care vaccines such as Shingrix.

Differentiator

Problem solved

Functional benefit

Brands

  • Amezosvatein: Lead investigational product, a non-mRNA adjuvanted subunit vaccine (also known as CRV-101) for the prevention of shingles (herpes zoster) in adults and chickenpox (varicella) in children, targeting glycoprotein E (gE) with a TLR4 agonist adjuvant.

Products and services

  • Amezosvatein (CRV-101) for Shingles A non-mRNA, adjuvanted subunit vaccine (also known by development code CRV-101) targeting glycoprotein E (gE) on the varicella zoster virus (VZV) for the prevention of shingles (herpes zoster) in adults aged 50 and older. Uses a synthetic TLR4 agonist (SLA) adjuvant formulated as a stable emulsion (SLA-SE) to deliver immune response non-inferior to Shingrix with significantly lower reactogenicity (7.3% Grade 2/3 reactogenicity at highest dose vs 33.3% for Shingrix, p<0.001). Phase 2 data (NCT05304351, 876 patients) met both primary immunogenicity and safety endpoints; a Phase 2 extension in adults over 70 was enrolling in mid-2025 in preparation for Phase 3.
  • Amezosvatein for Chickenpox (Varicella) Investigational application of amezosvatein for the prevention of chickenpox (varicella) in children, particularly targeting immunocompromised children for whom current live-attenuated virus (LAV) chickenpox vaccines are difficult to administer. As a non-live, adjuvanted subunit vaccine, amezosvatein is positioned to address limitations of existing LAV vaccines for children with cancer, organ transplants, or genetic or acquired immune deficiencies. Phase 1 trial in immunocompromised children is planned.

Quantifiable outcome

  • 7.3% Grade 2/3 reactogenicity events at highest dose vs 33.3% for Shingrix (p<0.001); more than half reduction in side effects
  • +7 more outcomes

Companies that use Curevo

Customer profile

Named customers1 record

Ideal customer profiles3 records

Curevo technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Curevo partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered flagship (acquirer), strategic advisor (m&a), strategic advisor (legal), core (technology developer), flagship (board chair), flagship (founding investor and licensor) and flagship (technology licensor).

  • Eli Lilly and Companyflagship (acquirer)Strategic or Co-development Partner · 26 May 2026Definitive agreement announced May 26, 2026 for Eli Lilly to acquire Curevo Inc. for up to $1.5 billion in cash (inclusive of upfront and milestone payments), subject to customary closing conditions including Hart-Scott-Rodino antitrust review. Lilly's global development and commercialization capabilities will accelerate and expand amezosvatein's potential. Relationship is Mutual — strategic acquirer providing commercialization capabilities while advancing Curevo's lead asset into Phase 3 and global markets.
  • Centerview Partners LLCstrategic advisor (m&a)Implementation/ SI/ Consulting Partner · 26 May 2026Acting as one of two financial advisors to Curevo for the sale to Eli Lilly announced May 26, 2026. Relationship is We to Them — Curevo engages Centerview Partners as financial advisor.
  • J.P. Morgan Securities LLCstrategic advisor (m&a)Implementation/ SI/ Consulting Partner · 26 May 2026Acting as one of two financial advisors to Curevo for the sale to Eli Lilly announced May 26, 2026. Relationship is We to Them — Curevo engages J.P. Morgan Securities LLC as financial advisor.
  • Cooley LLPstrategic advisor (legal)Implementation/ SI/ Consulting Partner · 26 May 2026Acting as legal advisor to Curevo for the sale to Eli Lilly announced May 26, 2026. Relationship is We to Them — Curevo engages Cooley LLP as legal counsel.
  • Access to Advanced Health Institute (AAHI)core (technology developer)Strategic or Co-development Partner · 17 March 2025Seattle-based institute where the SLA-SE adjuvant formulation used in amezosvatein was developed. Relationship is Them to Us — AAHI developed the adjuvant technology used in Curevo's lead product.
  • Moncef Slaoui (Board Chair)flagship (board chair)Others · 17 March 2025Former Chief Scientific Advisor to Operation Warp Speed and nearly 30-year veteran of GlaxoSmithKline, Dr. Slaoui joined Curevo as Board Chair concurrent with the $110M Series B financing in March 2025. He was directly involved in GSK's vaccine pipeline leading to the creation of Shingrix, Cervarix, Mosquirix, Rotarix, and Synflorix. Relationship is Them to Us — high-profile individual advisor/chair.
  • GC Biopharma (formerly Green Cross Corporation)flagship (founding investor and licensor)Strategic or Co-development Partner · 18 May 2018Founding investor that established Curevo in 2017/2018 as part of its global market entry strategy, holding a 20.3% equity stake. GC Biopharma funded the Mogam Institute for Biomedical Research, which licensed amezosvatein to Curevo. In May 2026, GC Biopharma sold its entire 20.3% stake to Eli Lilly for approximately 459.9 billion won (~$303.92 million), with total Curevo acquisition up to $1.5 billion including milestone payments; GC Biopharma will also receive future royalty income. Relationship is Mutual — both a capital provider and strategic partner licensing the technology.
  • Mogam Institute for Biomedical Researchflagship (technology licensor)OEM/ Whitelabel/ Licensing Partner · 1 January 2017Research institute funded by South Korea's GC Biopharma from which amezosvatein was licensed. Relationship is Them to Us — Mogam is the licensor of the technology that forms Curevo's lead asset.

Scale indicators11 records

Recent moves6 records

Expansion highlights6 records

Curevo competitors and assessment

Company assessment

Broad incumbents

  • GSK (Shingrix): GlaxoSmithKline markets Shingrix, the dominant shingles vaccine that Curevo's lead asset amezosvatein is positioned head-to-head against in Phase 2/3 trials. Shingrix is the standard of care Curevo is differentiated against.
  • Pfizer: Pfizer has a broad vaccine portfolio (Comirnaty partnership with BioNTech, Prevnar, etc.) and is also developing mRNA shingles vaccine candidates. Major incumbent vaccine manufacturer that Curevo will compete with globally.
  • Sanofi Pasteur: Global vaccine business and Sanofi Ventures is a Curevo Series B investor. Sanofi Pasteur develops competing vaccines across multiple infectious disease indications and represents a strategic incumbent with manufacturing and commercial scale.
  • Merck & Co. Major incumbent vaccine manufacturer with shingles franchise (Zostavax predecessor) and broad infectious disease pipeline. Merck is a potential global launch partner or acquirer for shingles assets.

Emerging players

  • Moderna: Moderna is developing mRNA-based shingles vaccine candidates, representing a direct future competitive threat to Curevo's non-mRNA amezosvatein. Former Moderna CMO Tal Zaks now sits on Curevo's board, illustrating the cross-competition dynamic.
  • VBI Vaccines: Clinical-stage biotech developing VBI-2601, an enveloped virus-like particle (eVLP) shingles vaccine candidate. Direct competitor in the next-generation shingles vaccine space with a different technology platform.
  • BioNTech: Partnered with Pfizer on Comirnaty and developing mRNA-based shingles vaccine candidates. Represents a future competitive threat to amezosvatein if mRNA shingles products reach approval first.

Direct peers

  • Vaxcyte: Clinical-stage vaccine company developing non-mRNA, adjuvanted subunit vaccines with similar technology approach (synthetic conjugates). Also backed by Medicxi, with Moncef Slaoui as Board Chair. Direct peer in next-generation non-mRNA vaccine development.
  • Dynavax Technologies: Specializes in adjuvant technology (CpG 1018 used in Heplisav-B hepatitis B vaccine) and vaccine development. Comparable to Curevo in being an adjuvant-platform-focused vaccine company with adjuvanted subunit products.
  • Novavax: Develops adjuvanted recombinant protein subunit vaccines (Nuvaxovid COVID vaccine, Matrix-M adjuvant). Strong technology parallel to Curevo's adjuvanted subunit approach and represents a peer in non-mRNA vaccine commercialization.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Curevo social profiles

Digital presence

Curevo financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Curevo leadership team

Management profile

Number of profiles

Profiles13 records

Curevo funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors9 records

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

Curevo 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 Curevo

What does Curevo do?

Curevo is developing amezosvatein (also known by development code CRV-101), a single non-mRNA, adjuvanted subunit vaccine candidate applied to two indications: prevention of shingles (herpes zoster) in adults aged 50 and older, and prevention of chickenpox (varicella) in immunocompromised children. The lead shingles program has completed an 876-patient Phase 2 head-to-head trial versus GSK's Shingrix meeting both primary immunogenicity non-inferiority and safety endpoints, and is Phase 3-ready; the chickenpox program is positioned as a Phase 1 application for immunocompromised pediatric populations.

Is Curevo a public or private company?

Curevo is a private company. It is classified as venture growth investor backed and is currently acquired.

When was Curevo founded?

Curevo was founded in 2018. It employs 11 to 50 people.

Where is Curevo based?

Curevo is headquartered in Bothell, United States, in the North America region.

How does Curevo make money?

Two revenue lines are on record. Acquisition / Liquidity Event is the primary driver. The others are private Equity Financing.

Who are Curevo's main competitors?

Broad incumbents on record are GSK (Shingrix), Pfizer, Sanofi Pasteur and Merck & Co.. Emerging players are Moderna, VBI Vaccines and BioNTech. Direct peers are Vaxcyte, Dynavax Technologies and Novavax.

Does Curevo have an API?

No public API is recorded for Curevo.

What industry is Curevo in?

Curevo's product category is Infectious Disease Vaccines. Its primary akta.pro industry code is HLAAAEAA, Prophylactic Human Vaccines (routine, pediatric, adult), with a secondary code of HLAAAEAK, Clinical Development & Regulatory for Vaccines (trials, pharmacovigilance, lot release). Its NAICS code is 62151 and its SIC code is 2835.

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ChosunbizGC Biopharma secures KRW 286.8b from Lilly in Curevo sale, boosts Q3 profitGC Biopharma received $189.52 million upfront from Eli Lilly for its Curevo equity sale, with the remaining $14.5 million expected after settlement. The company will recognize the upfront payment as Q3 net profit and plans to invest in future growth businesses.Labiotech.euThe Naming Patterns Behind 12,000 Biotech CompaniesAn analysis of over 12,000 biotech company names found that names beginning with A, C, or S are most common across categories, while Q, W, X, Y, and Z are least common. Exceptions exist in microbiome and psychedelics sectors, where M, E, P, S, and B dominate. The pattern likely stems from pre-internet directory preferences and broader naming trends.Labiotech.euTop biotech deals in May 2026May 2026 saw significant biotech M&A and licensing activity, with Angelini Pharma acquiring Catalyst Pharmaceuticals for $4.1 billion, Bayer buying Perfuse Therapeutics for $2.45 billion, and UCB purchasing Candid Therapeutics for $2.2 billion. Eli Lilly made four acquisitions totaling up to $3.8 billion (Curevo, LimmaTech Biologics, Vaccine Company, Engage Bio), while Bristol Myers Squibb entered a landmark $15.2 billion licensing deal with Hengrui Pharma for 13 early-stage oncology, hematology, and immunology programs.The Motley FoolLilly Just Announced 3 Infectious Disease Acquisitions in 1 Day. Is This the Beginning of Its Post-Obesity Growth Strategy?Eli Lilly announced three infectious disease acquisitions on the same day, including Curevo, LimmaTech Biologics, and Vaccine Company, potentially costing over $3.8 billion. The deals target vaccines for shingles, bacterial pathogens, and EBV, with potential annual sales of hundreds of millions to billions. The acquisitions signal Lilly's shift toward preventive medicine beyond its obesity franchise.The Motley Fool3 Reasons Eli Lilly Remains a BuyEli Lilly spent $3.83 billion on three biotech companies, including Curevo, LimmaTech, and the Vaccine Company, to expand its pipeline. The company's GLP-1 franchise and high-margin specialty drugs have driven a 45% share gain over the past year. Management forecasts 2026 revenue of $82-85 million and EPS of $35.50-37.The Motley FoolForget Weight Loss Drugs: Here Is Another Reason to Buy Eli Lilly StockEli Lilly is expanding beyond its weight-loss focus by acquiring three vaccine-focused biotechs for up to $3.8 billion. The company also reports strong sales growth in other areas like eczema and Alzheimer's drugs, and a non-opioid pain candidate. These moves aim to reduce reliance on its weight-loss market as competition grows.RTTNewsLilly Continues Its Acquisition Spree, Inks Two Asia Partnerships TodayEli Lilly announced two new Asian licensing agreements on June 1, 2026, securing exclusive worldwide rights to select programs from Haisco Pharmaceutical Group for $87 million upfront and up to $2.97 billion in milestones, and a global licensing deal with Hanmi Pharmaceutical for Sonefpeglutide with $75 million upfront and up to $1.185 billion in milestones. The deals follow Lilly's May 26, 2026 announcement of three infectious disease acquisitions — Curevo Inc., LimmaTech Biologics AG, and Vaccine Company, Inc. — with combined potential values exceeding $3.8 billion. The strategy positions Lilly to expand its metabolic and autoimmune pipeline through Asian partnerships while reinforcing its infectious-disease franchise through vaccine-focused acquisitions.TheStreet.comEli Lilly sends strong message on vaccine strategyEli Lilly announced deals to acquire three vaccine companies for up to $3.83 billion, targeting shingles, antibiotic-resistant bacteria, and Epstein-Barr virus vaccines. The company's chief scientific officer cited new research linking infections to dementia and cancer, making this its most aggressive push into infectious disease prevention in 150 years.PhirdaBreaking news! Nearly $4 billion spent to acquire three pharmaceutical companies, Eli Lilly returns to the vaccine race.Eli Lilly announced on May 26 an agreement to acquire Curevo, LimmaTech Biologics, and Vaccine Company for nearly $4 billion. The deal targets vaccine platforms for shingles, drug-resistant bacteria, and EBV, with Curevo valued at $1.5 billion, LimmaTech at up to $780 million, and Vaccine Company at up to $1.55 billion. The acquisition aims to expand Eli Lilly's preventive vaccine pipeline.pharmaphorumLilly gets back in infectious disease, via three M&A dealsEli Lilly has agreed to acquire three companies—Curevo, LimmaTech Biologics, and Vaccine Company—for more than $3.8 billion, marking the pharmaceutical company's return to infectious disease after exiting the category approximately seven years ago. The deals include a $1.5 billion deal for Curevo and its shingles vaccine candidate (CRV-101) being tested head-to-head against GSK's blockbuster Shingrix, an $780 million acquisition of LimmaTech focused on bacterial vaccines targeting antimicrobial-resistant pathogens, and the purchase of Vaccine Company and its nanoparticle vaccine platform targeting Epstein-Barr virus. The acquisitions represent a deliberate strategic shift toward disease prevention rather than treatment, building on Lilly's recent acquisition spree in 2026 totaling tens of billions of dollars in deal value.