Synklino
Synklino A/S is a Danish clinical-stage biotechnology company developing SYN002, a first-in-class ex vivo therapeutic fusion protein that eliminates cytomegalovirus from donor kidneys during machine perfusion, targeting latent and active CMV infection in kidney transplant recipients.
- Company typePrivate
- Founded2017
- HeadquartersLyngby, Denmark
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Synklino does
Synklino A/S is a Danish clinical-stage biotechnology company founded in July 2017 as a spinout from the University of Copenhagen and the Technical University of Denmark, headquartered at Frederiksborggade 1, Copenhagen K. The company is developing a single lead product, SYN002, a first-in-class therapeutic fusion protein (immunotoxin) designed to eliminate cytomegalovirus (CMV) infection in donor kidneys prior to transplantation. SYN002 targets US28, a CMV-encoded membrane receptor exclusively expressed on virus-infected cells during both lytic and latent phases, and is administered ex vivo during normothermic machine perfusion, treating the donor organ directly without exposing the transplant recipient to systemic therapy.
SYN002 addresses a clear unmet need: approximately 30% of kidney transplant recipients receiving CMV-positive donor organs still experience CMV reactivation despite standard antiviral prophylaxis, leading to increased morbidity, mortality, organ rejection, and a roughly 50% rise in transplant-related costs. Preclinical data published in the American Journal of Transplantation demonstrated greater than 90% reduction in CMV reactivation from latency in treated human donor kidneys. Synklino retains broad intellectual property rights to SYN002 and its ex vivo use in organ perfusion, built on a decade of academic research from its founding universities. The company initiated first-in-human Phase 1 clinical trials in 2026, with the first patient dosed in May 2026 at the Ajmera Transplant Centre, University Health Network Toronto, under Principal Investigator Prof. Atul Humar.
The business model is licensing- and partnership-driven: Synklino intends to develop SYN002 through proof-of-concept and then partner with established pharmaceutical companies for late-stage development and global commercialization, generating revenue from upfront payments, development milestones, and royalties. The company has raised approximately EUR 43.8 million in total across a 2019 BioInnovation Institute grant (DKK 10m), a 2020 seed round (Eir Ventures and Vaekstfonden), a heavily oversubscribed 2021 financing round (DKK 106m/EUR 14m), and a 2022 Series A of EUR 29.8m led by PKA pension fund with Vaekstfonden and Eir Ventures. Ownership includes approximately 70 private shareholders alongside institutional investors. The company is privately held, pre-revenue, and has 11–50 employees.
Synklino firmographics
Firmographics- Name
- Synklino
- Legal name
- Synklino A/S
- Website
- https://synklino.com
- Company type
- Private
- Founded year
- 2017
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Synklino A/S is a Danish clinical-stage biotechnology company developing SYN002, a first-in-class ex vivo therapeutic fusion protein that eliminates cytomegalovirus from donor kidneys during machine perfusion, targeting latent and active CMV infection in kidney transplant recipients.
- Ownership category
- akta.pro rank
Synklino industry classification
Industry- Product category
- Transplant Therapeutics
- NAICS
- Research and Development in Biotechnology (except Nanobiotechnology) (541714)
- SIC
- In Vitro & In Vivo Diagnostic Substances (2835)
- akta.pro primary industry
- Fusion Proteins & Fc-Engineered Biologics (HLAAAAAD)
- akta.pro secondary industry
- Engineered Protein Therapeutics (de novo/AI-designed proteins, novel scaffolds) (HLAAAAAJ)
Keywords
Where Synklino is headquartered
LocationHeadquarters
- HQ city
- Lyngby
- HQ country
- Denmark
- HQ region
- Europe
Offices1 record
Markets served
Synklino business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Pharmaceutical Licensing/Partnership: As a clinical-stage biotech, Synklino plans to develop SYN002 through proof-of-concept, after which they expect to partner with established pharma companies for late-stage development and commercialisation. Revenue will come from licensing deals, milestone payments, and royalties from commercial partners.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels4 records
Synklino product offering
Product offeringCore offering
Synklino develops SYN002, a first-in-class therapeutic fusion protein (immunotoxin) that targets the CMV-encoded US28 membrane receptor to eliminate both active and latent cytomegalovirus-infected cells in donor kidneys. The drug is administered ex vivo during normothermic machine perfusion of the donor organ prior to transplantation, treating the organ directly so the transplant recipient is not exposed to systemic antiviral therapy. The company is currently advancing SYN002 through a Phase 1 clinical trial at University Health Network Toronto.
Product overview
Synklino is a Danish clinical-stage biotechnology company developing a single lead product, SYN002, a first-in-class ex vivo therapy for preventing cytomegalovirus (CMV) reactivation in kidney transplant recipients. SYN002 is a therapeutic fusion protein administered during ex vivo organ perfusion (machine perfusion) prior to transplantation, enabling direct treatment of the donor organ without systemic exposure to the recipient. The company is currently advancing SYN002 through Phase 1 clinical development and has no additional commercial products or services.
Differentiator
Problem solved
Functional benefit
Products and services
- SYN002 First-in-class therapeutic fusion protein (immunotoxin) that targets the CMV-encoded US28 membrane receptor on infected cells to eliminate both active (lytic) and latent cytomegalovirus from donor kidneys. Administered ex vivo during normothermic machine perfusion of the donor organ prior to transplantation, treating the donor organ directly so the transplant recipient is not exposed to systemic antiviral therapy. Intended for kidney transplant centers and their CMV-positive donor kidney recipients.
Quantifiable outcome
- >90% reduction in CMV reactivation from latency in human kidneys treated ex vivo
- +3 more outcomes
Companies that use Synklino
Customer profileNamed customers1 record
Segments2 records
Ideal customer profiles2 records
Synklino technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature3 records
Synklino partnerships and signals
Strategic signalPartnerships
Four partnerships are on record, tiered core.
- University Health Network (UHN), TorontocoreAjmera Transplant Centre at UHN is conducting the Phase 1 clinical trial of SYN002. One of the world's leading transplant centers, performing more than 600 solid organ transplants each year. Study led by Professor Atul Humar, internationally recognized for work in transplant infectious diseases.
- University of Cambridge / Addenbrooke's HospitalcoreCollaboration with Professor Michael Nicholson's group for preclinical proof-of-concept studies in human donor kidneys. Professor Nicholson is Director of the NIHR Blood and Transplant Research Unit (BTRU) in Organ Donation and Transplantation and serves as Lead Coordinating Investigator for the UK Phase 1 trial.
- Professor Atul HumarcorePrincipal Investigator of Phase 1 trial at UHN. Director at University of Toronto Transplant Institute (largest multi-organ transplantation centre in North America). Member of Synklino's Scientific Advisory Board since October 2020. Internationally recognized expert in transplant infectious diseases and CMV prevention.
- Professor John SinclaircoreMember of Synklino's Scientific Advisory Board. Deputy Head of the Department of Medicine and Head of the Division of Infectious Diseases at Cambridge University. Expert on CMV life cycle, especially during latency.
Scale indicators6 records
Recent moves7 records
Expansion highlights5 records
Synklino competitors and assessment
Company assessmentDirect peers
- Atara Biotherapeutics: Allogeneic T-cell therapy company with programs targeting viral infections in immunocompromised transplant patients, including CMV. Comparable in transplant-focused virology space and clinical-stage biotech profile, but uses cell therapy rather than a fusion protein.
- AlloVir: Developed Viralym-M (now spun out as Kalaris Therapeutics), an allogeneic, multi-virus-specific T-cell therapy for transplant patients including those with refractory CMV. Closely comparable target patient population (transplant recipients with viral reactivation) and clinical-stage profile.
- Hookipa Pharma: Clinical-stage biotech developing HB-101, a CMV vaccine designed to prevent CMV reactivation in transplant recipients. Directly comparable to Synklino in target indication (post-transplant CMV), patient population, and clinical-stage biotech profile, though Hookipa uses a vaccine rather than an ex vivo immunotoxin approach.
- Helocyte Pharmaceuticals: Developing Triplex, a therapeutic CMV vaccine for use in stem cell and solid organ transplant recipients. Comparable in targeting CMV prevention in transplant recipients and clinical-stage biotech profile, though using a vaccine modality.
Broad incumbents
- Merck & Co. Markets Prevymis (letermovir), the leading branded antiviral for CMV prophylaxis in adult CMV-seropositive transplant recipients. Represents the incumbent standard of care against which SYN002 will compete; broad incumbent with multiple therapeutic areas.
- Takeda Pharmaceutical: Markets Livtencity (maribavir), the first FDA-approved treatment for post-transplant CMV infection/disease refractory to existing antivirals. Directly competes with SYN002's indication and is a relevant potential strategic partner given its transplant franchise.
- Moderna: Developing mRNA-1647, an mRNA-based CMV vaccine currently in Phase 3 trials, the most advanced CMV vaccine program. Compares to Synklino in CMV prevention but as a much larger, late-stage company pursuing an in vivo vaccine approach rather than ex vivo biologic.
Emerging players
- VBI Vaccines: Developed VBI-1501, a CMV vaccine candidate that entered Phase 1 clinical evaluation. Comparable in targeting CMV with an immunotherapeutic approach, though VBI is broader and earlier-stage in the transplant CMV space.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
Synklino social profiles
Digital presenceSynklino financial estimates
Financial estimateRevenue estimate
Valuation estimate
Synklino leadership team
Management profileNumber of profiles
Profiles7 records
Synklino funding detail
Funding detailFunding overview
Funding rounds3 records
Investors5 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Synklino M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Synklino
What does Synklino do?
Synklino develops SYN002, a first-in-class therapeutic fusion protein (immunotoxin) that targets the CMV-encoded US28 membrane receptor to eliminate both active and latent cytomegalovirus-infected cells in donor kidneys. The drug is administered ex vivo during normothermic machine perfusion of the donor organ prior to transplantation, treating the organ directly so the transplant recipient is not exposed to systemic antiviral therapy. The company is currently advancing SYN002 through a Phase 1 clinical trial at University Health Network Toronto.
Is Synklino a public or private company?
Synklino is a private company. It is classified as venture growth investor backed and is currently operating.
When was Synklino founded?
Synklino was founded in 2017. It employs 11 to 50 people.
Where is Synklino based?
Synklino is headquartered in Lyngby, Denmark, in the Europe region.
How does Synklino make money?
One revenue line is on record: pharmaceutical Licensing/Partnership.
Who are Synklino's main competitors?
Direct peers on record are Atara Biotherapeutics, AlloVir, Hookipa Pharma and Helocyte Pharmaceuticals. Broad incumbents are Merck & Co., Takeda Pharmaceutical and Moderna. VBI Vaccines is listed as an emerging player.
Does Synklino have an API?
No public API is recorded for Synklino.
What industry is Synklino in?
Synklino's product category is Transplant Therapeutics. Its primary akta.pro industry code is HLAAAAAD, Fusion Proteins & Fc-Engineered Biologics, with a secondary code of HLAAAAAJ, Engineered Protein Therapeutics (de novo/AI-designed proteins, novel scaffolds). Its NAICS code is 541714 and its SIC code is 2835.