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SillaJen

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uuid0006b95

Namestring
SillaJen
Legal namestring
SillaJen Co., Ltd.
Websiteurl
sillajen.com
Company typeenum
Public
Founded yearint
2016
Descriptiontext

SillaJen Co., Ltd. (KOSDAQ: 215600) is a clinical-stage biopharmaceutical company developing engineered oncolytic immunotherapies for solid tumors. Its core technology is a vaccinia virus backbone modified to selectively infect and replicate in cancer cells — exploiting tumor-specific genetic changes to cause tumor debulking, vascular shutdown, and systemic anti-tumor immune activation — supported by proprietary SOLVE and GEEV platforms. The lead asset, Pexa-Vec (JX-594), is in a Phase 3 trial in China for hepatocellular carcinoma (via Lee's Pharmaceutical) and in a Phase 2 combination trial with Regeneron's Libtayo for renal cell carcinoma, with a CSR submitted to the U.S. FDA for the REN026 RCC study in March 2026. The pipeline extends to BAL0891, a first-in-class dual TTK/PLK1 inhibitor in Phase 1, the next-generation SJ-600 series (Wyeth strain, including SJ-650) engineered for systemic IV delivery with complement-evasion proteins, and the JX-900 series led by JX-970 in preclinical development.

The company is headquartered in Seoul with a research center in Yongin (Gwanggyo) and a wholly-owned U.S. subsidiary, SillaJen Biotherapeutics, in San Francisco handling clinical operations, regulatory affairs, R&D, manufacturing, and alliance management. With 51–100 employees and no commercial product, SillaJen operates a licensing- and partnership-led business model: revenue is generated through milestone and collaboration payments from a small set of partners rather than product sales. 2021 revenue was KRW 254 million (a steep decline from KRW 9,068 million in 2019), but the company reported KRW 20.35 billion of operating profit and KRW 16 billion of net profit that year, reflecting non-operating items rather than commercial scaling. Co-CEOs Han Sang-gyu and Park Sang-geun currently lead the company, which faces KOSDAQ delisting-rule pressure that has driven inbound interest — including non-binding 2026 discussions with OSR Holdings / Vaximm AG over a Pexa-Vec license and a potential ~16% equity stake.

Short descriptiontext

SillaJen is a clinical-stage South Korean biopharmaceutical company (KOSDAQ: 215600) developing engineered oncolytic immunotherapies — including lead asset Pexa-Vec (JX-594) — for solid tumors, generating revenue through licensing and partnership deals with pharmaceutical companies rather than product sales.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersSan Francisco, United States
HQ citystring
San Francisco
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
oncolytic immunotherapy, cancer therapeutics, biopharmaceutical development, oncolytic virus platform, immuno-oncology drugs
Industry3 codes
1Therapeutic Vaccines (cancer, chronic infection immunotherapy)
CodeHLAAAEABPrimaryYes
2Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches)
CodeHLAAACAFPrimaryNo
3Vaccine Technology Platforms (mRNA, viral vector, protein subunit, inactivated/live-attenuated, VLP, DNA)
CodeHLAAAEADPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Oncolytic Immunotherapy
No data
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Licensing and Partnership Revenue
TypeLicensing Royalties
Description

SillaJen generates revenue through licensing agreements and partnerships with pharmaceutical companies for its clinical-stage oncolytic immunotherapy candidates including Pexa-Vec, BAL0891, and the SJ-600 series.

sillajen.com
2Revenue Growth Post-Acquisition
TypeLicensing Royalties
Description

The company achieved significant revenue growth following acquisitions as part of defensive M&A strategy to meet KOSDAQ listing requirements.

en.sedaily.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components3 values
Personnel, Technology or R&D, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

SillaJen is a clinical-stage biopharmaceutical company developing engineered oncolytic immunotherapies that selectively infect, replicate in, and destroy cancer cells while stimulating anti-tumor immune response. Core assets include Pexa-Vec (JX-594) in Phase 3 (PHOCUS) for liver cancer and Phase 2 for renal cell carcinoma, BAL0891 (a first-in-class dual TTK/PLK1 inhibitor) in Phase 1, and the SJ-600 series of next-generation oncolytic vaccinia viruses engineered for systemic intravenous delivery with complement evasion capability. The company operates through licensing and co-development partnerships with pharmaceutical companies rather than direct product sales.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Significant revenue growth following acquisitions
Product overview1 text field

SillaJen is a South Korean biopharmaceutical company developing a portfolio of oncolytic immunotherapies for cancer treatment. The core product is Pexa-Vec (JX-594), a clinical-stage oncolytic virus engineered to selectively infect and replicate in cancer cells. The pipeline includes BAL0891, a dual TTK/PLK inhibitor for solid tumors in Phase 1 trials; the SJ-600 series (Wyeth Strain Backbone), a next-generation platform for improved intravenous delivery of oncolytic viruses including SJ-650; and the JX-900 series (including JX-970), representing next-generation candidates. The company operates through its Seoul headquarters, Gwanggyo research center, and San Francisco subsidiary SillaJen Biotherapeutics, which handles clinical operations, regulatory affairs, R&D, manufacturing, and alliance management for clinical trials.

Product and service5 records
1Pexa-Vec (JX-594)
CategoryClinical-stage oncolytic immunotherapy
Description

An engineered oncolytic immunotherapy designed to selectively infect and replicate in cancer cells, causing vascular shutdown in tumor blood vessels and stimulating immune response against cancer cells. Licensed to partners such as Regeneron (for combination with Libtayo in RCC) and Lee's Pharmaceutical (for liver cancer in China).

2BAL0891
CategoryClinical-stage small-molecule cancer therapeutic
Description

A dual TTK/PLK inhibitor targeting two key phosphorylating enzymes involved in mitotic checkpoint; induces mitotic override and mitotic block to disrupt cancer cell cycle and trigger apoptosis. The only molecule in development simultaneously inhibiting both TTK and PLK1.

3SJ-600 Series
CategoryNext-generation oncolytic virus platform
Description

Next-generation platform of oncolytic vaccinia viruses engineered for systemic (intravenous) delivery, expressing proteins on the viral envelope that inhibit antiviral substances (including complement activation) to improve ability to reach tumors and enable repeat dosing.

4SJ-650
CategoryOncolytic vaccinia virus candidate (systemic delivery)
Description

An oncolytic vaccinia virus engineered for systemic (intravenous) delivery, expressing a protein on the viral envelope that inhibits complement activation to improve tumor targeting and enable repeat dosing.

5JX-970 (JX-900 Series)
CategoryNext-generation oncolytic virus pipeline
Description

Next-generation oncolytic virus pipeline candidate (JX-900 series) that demonstrated tumor debulking effect and selective preference for tumor tissues in preclinical studies.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierPotentialTypeStrategic or Co-development PartnerAnnounced on2026-03-16
Description

Ongoing but non-binding discussions regarding potential licensing arrangement for Pexa-Vec (clinical-stage oncolytic immunotherapy for renal cell carcinoma) and preliminary discussions about acquiring approximately 16% of SillaJen's outstanding common shares. No agreement on deal structure, terms, or financing has been reached.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Clinical trial collaboration for Pexa-Vec in combination with Regeneron's Libtayo (cemiplimab-rwlc) for renal cell carcinoma treatment. First patient enrolled in Part 2 of the renal cell carcinoma trial evaluating the combination therapy.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Partnership for PHOCUS trial - Phase 3 clinical trial for Pexa-Vec in liver cancer in China. Lee's Pharmaceutical is responsible for clinical development and commercialization in China.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biotech developing engineered oncolytic viruses (RP1, RP2, RP3) for solid tumors. Most direct comparable to SillaJen in oncolytic immunotherapy modality, clinical stage, and pipeline breadth.

TypeDirect peer
Description

French clinical-stage biotech developing oncolytic viruses (TG6002, TG4050) and listed as a SillaJen partnership contact. Comparable virus-based immunotherapy platform and clinical-stage strategy.

TypeBroad incumbent
Description

Leading IO incumbent with Keytruda (pembrolizumab) and extensive combination trials in oncology. Comparable as the dominant combination-IO partner for next-generation oncolytic virus developers.

TypeEmerging player
Description

Emerging biotech developing oncolytic adenoviruses engineered for tumor-selective replication and immune stimulation. Comparable smaller-scale peer in engineered oncolytic virus immunotherapy.

TypeBroad incumbent
Description

Major oncology incumbent with leading checkpoint inhibitor franchises (Opdivo, Yervoy) frequently evaluated in combination with oncolytic viruses. Sets the competitive standard for combination-IO treatment paradigms.

TypeDirect peer
Description

Develops pelareorep, a systemically delivered oncolytic virus for multiple solid tumor indications. Comparable clinical-stage oncolytic virus modality, though focused on a different virus class.

TypeOthers
Description

Direct partner of SillaJen on the Pexa-Vec + Libtayo RCC combination trial. Relevant as the incumbent checkpoint inhibitor partner validating SillaJen's combination strategy and a potential acquirer/co-developer.

TypeBroad incumbent
Description

Approved the first oncolytic immunotherapy (Imlygic/T-VEC) and is a major oncology player. Comparable as the established benchmark for oncolytic virus commercialization and combination-IO strategies.

TypeDirect peer
Description

Clinical-stage developer of proprietary oncolytic virus platforms (Olvi-Vec and others) for cancer immunotherapy. Directly comparable in modality, clinical-stage positioning, and focus on next-generation viral delivery.

TypeEmerging player
Description

Clinical-stage developer of VCN-01 and other oncolytic adenoviruses for solid tumors. Emerging comparable in the oncolytic virus space with a similar combinatorial IO strategy.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat2 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 customers1 record

Each record includes

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

Segment1 record

Each record includes

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

Ideal customer profile2 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

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

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

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

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

Investors1 record

Each record includes

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

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

M&A1 record

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 →

SillaJen

Oncolytic Immunotherapysillajen.com

SillaJen is a clinical-stage South Korean biopharmaceutical company (KOSDAQ: 215600) developing engineered oncolytic immunotherapies — including lead asset Pexa-Vec (JX-594) — for solid tumors, generating revenue through licensing and partnership deals with pharmaceutical companies rather than product sales.

What SillaJen does

SillaJen Co., Ltd. (KOSDAQ: 215600) is a clinical-stage biopharmaceutical company developing engineered oncolytic immunotherapies for solid tumors. Its core technology is a vaccinia virus backbone modified to selectively infect and replicate in cancer cells — exploiting tumor-specific genetic changes to cause tumor debulking, vascular shutdown, and systemic anti-tumor immune activation — supported by proprietary SOLVE and GEEV platforms. The lead asset, Pexa-Vec (JX-594), is in a Phase 3 trial in China for hepatocellular carcinoma (via Lee's Pharmaceutical) and in a Phase 2 combination trial with Regeneron's Libtayo for renal cell carcinoma, with a CSR submitted to the U.S. FDA for the REN026 RCC study in March 2026. The pipeline extends to BAL0891, a first-in-class dual TTK/PLK1 inhibitor in Phase 1, the next-generation SJ-600 series (Wyeth strain, including SJ-650) engineered for systemic IV delivery with complement-evasion proteins, and the JX-900 series led by JX-970 in preclinical development.

The company is headquartered in Seoul with a research center in Yongin (Gwanggyo) and a wholly-owned U.S. subsidiary, SillaJen Biotherapeutics, in San Francisco handling clinical operations, regulatory affairs, R&D, manufacturing, and alliance management. With 51–100 employees and no commercial product, SillaJen operates a licensing- and partnership-led business model: revenue is generated through milestone and collaboration payments from a small set of partners rather than product sales. 2021 revenue was KRW 254 million (a steep decline from KRW 9,068 million in 2019), but the company reported KRW 20.35 billion of operating profit and KRW 16 billion of net profit that year, reflecting non-operating items rather than commercial scaling. Co-CEOs Han Sang-gyu and Park Sang-geun currently lead the company, which faces KOSDAQ delisting-rule pressure that has driven inbound interest — including non-binding 2026 discussions with OSR Holdings / Vaximm AG over a Pexa-Vec license and a potential ~16% equity stake.

SillaJen firmographics

Firmographics
Name
SillaJen
Legal name
SillaJen Co., Ltd.
Website
https://sillajen.com
Company type
Public
Founded year
2016
Operating status
Operating
Headcount range
51–100 employees
Short description
SillaJen is a clinical-stage South Korean biopharmaceutical company (KOSDAQ: 215600) developing engineered oncolytic immunotherapies — including lead asset Pexa-Vec (JX-594) — for solid tumors, generating revenue through licensing and partnership deals with pharmaceutical companies rather than product sales.
Ownership category
akta.pro rank

SillaJen industry classification

Industry
Product category
Oncolytic Immunotherapy
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Therapeutic Vaccines (cancer, chronic infection immunotherapy) (HLAAAEAB)
akta.pro secondary industries
Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches) (HLAAACAF), Vaccine Technology Platforms (mRNA, viral vector, protein subunit, inactivated/live-attenuated, VLP, DNA) (HLAAAEAD)

Keywords

  • Oncolytic immunotherapy
  • Cancer therapeutics
  • Biopharmaceutical development
  • Oncolytic virus platform
  • Immuno-oncology drugs

Where SillaJen is headquartered

Location

Headquarters

HQ city
San Francisco
HQ country
United States
HQ region
North America

Offices3 records

Markets served

SillaJen business model

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

Revenue model

  1. Licensing and Partnership Revenue: SillaJen generates revenue through licensing agreements and partnerships with pharmaceutical companies for its clinical-stage oncolytic immunotherapy candidates including Pexa-Vec, BAL0891, and the SJ-600 series.
  2. Revenue Growth Post-Acquisition: The company achieved significant revenue growth following acquisitions as part of defensive M&A strategy to meet KOSDAQ listing requirements.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

SillaJen product offering

Product offering

Core offering

SillaJen is a clinical-stage biopharmaceutical company developing engineered oncolytic immunotherapies that selectively infect, replicate in, and destroy cancer cells while stimulating anti-tumor immune response. Core assets include Pexa-Vec (JX-594) in Phase 3 (PHOCUS) for liver cancer and Phase 2 for renal cell carcinoma, BAL0891 (a first-in-class dual TTK/PLK1 inhibitor) in Phase 1, and the SJ-600 series of next-generation oncolytic vaccinia viruses engineered for systemic intravenous delivery with complement evasion capability. The company operates through licensing and co-development partnerships with pharmaceutical companies rather than direct product sales.

Product overview

SillaJen is a South Korean biopharmaceutical company developing a portfolio of oncolytic immunotherapies for cancer treatment. The core product is Pexa-Vec (JX-594), a clinical-stage oncolytic virus engineered to selectively infect and replicate in cancer cells. The pipeline includes BAL0891, a dual TTK/PLK inhibitor for solid tumors in Phase 1 trials; the SJ-600 series (Wyeth Strain Backbone), a next-generation platform for improved intravenous delivery of oncolytic viruses including SJ-650; and the JX-900 series (including JX-970), representing next-generation candidates. The company operates through its Seoul headquarters, Gwanggyo research center, and San Francisco subsidiary SillaJen Biotherapeutics, which handles clinical operations, regulatory affairs, R&D, manufacturing, and alliance management for clinical trials.

Differentiator

Problem solved

Functional benefit

Products and services

  • Pexa-Vec (JX-594) An engineered oncolytic immunotherapy designed to selectively infect and replicate in cancer cells, causing vascular shutdown in tumor blood vessels and stimulating immune response against cancer cells. Licensed to partners such as Regeneron (for combination with Libtayo in RCC) and Lee's Pharmaceutical (for liver cancer in China).
  • BAL0891 A dual TTK/PLK inhibitor targeting two key phosphorylating enzymes involved in mitotic checkpoint; induces mitotic override and mitotic block to disrupt cancer cell cycle and trigger apoptosis. The only molecule in development simultaneously inhibiting both TTK and PLK1.
  • SJ-600 Series Next-generation platform of oncolytic vaccinia viruses engineered for systemic (intravenous) delivery, expressing proteins on the viral envelope that inhibit antiviral substances (including complement activation) to improve ability to reach tumors and enable repeat dosing.
  • SJ-650 An oncolytic vaccinia virus engineered for systemic (intravenous) delivery, expressing a protein on the viral envelope that inhibits complement activation to improve tumor targeting and enable repeat dosing.
  • JX-970 (JX-900 Series) Next-generation oncolytic virus pipeline candidate (JX-900 series) that demonstrated tumor debulking effect and selective preference for tumor tissues in preclinical studies.

Quantifiable outcome

  • Significant revenue growth following acquisitions

Companies that use SillaJen

Customer profile

Named customers1 record

Segments1 record

Ideal customer profiles2 records

SillaJen technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

SillaJen partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered potential and core.

  • OSR Holdings / Vaximm AGpotentialStrategic or Co-development Partner · 16 March 2026Ongoing but non-binding discussions regarding potential licensing arrangement for Pexa-Vec (clinical-stage oncolytic immunotherapy for renal cell carcinoma) and preliminary discussions about acquiring approximately 16% of SillaJen's outstanding common shares. No agreement on deal structure, terms, or financing has been reached.
  • RegeneroncoreStrategic or Co-development PartnerClinical trial collaboration for Pexa-Vec in combination with Regeneron's Libtayo (cemiplimab-rwlc) for renal cell carcinoma treatment. First patient enrolled in Part 2 of the renal cell carcinoma trial evaluating the combination therapy.
  • Lee's PharmaceuticalcoreStrategic or Co-development PartnerPartnership for PHOCUS trial - Phase 3 clinical trial for Pexa-Vec in liver cancer in China. Lee's Pharmaceutical is responsible for clinical development and commercialization in China.

Scale indicators6 records

Recent moves6 records

Expansion highlights5 records

SillaJen competitors and assessment

Company assessment

Direct peers

  • Replimune: Clinical-stage biotech developing engineered oncolytic viruses (RP1, RP2, RP3) for solid tumors. Most direct comparable to SillaJen in oncolytic immunotherapy modality, clinical stage, and pipeline breadth.
  • Transgene: French clinical-stage biotech developing oncolytic viruses (TG6002, TG4050) and listed as a SillaJen partnership contact. Comparable virus-based immunotherapy platform and clinical-stage strategy.
  • Oncolytics Biotech: Develops pelareorep, a systemically delivered oncolytic virus for multiple solid tumor indications. Comparable clinical-stage oncolytic virus modality, though focused on a different virus class.
  • Genelux Corporation: Clinical-stage developer of proprietary oncolytic virus platforms (Olvi-Vec and others) for cancer immunotherapy. Directly comparable in modality, clinical-stage positioning, and focus on next-generation viral delivery.

Broad incumbents

  • Merck & Co. Leading IO incumbent with Keytruda (pembrolizumab) and extensive combination trials in oncology. Comparable as the dominant combination-IO partner for next-generation oncolytic virus developers.
  • Bristol-Myers Squibb: Major oncology incumbent with leading checkpoint inhibitor franchises (Opdivo, Yervoy) frequently evaluated in combination with oncolytic viruses. Sets the competitive standard for combination-IO treatment paradigms.
  • Amgen: Approved the first oncolytic immunotherapy (Imlygic/T-VEC) and is a major oncology player. Comparable as the established benchmark for oncolytic virus commercialization and combination-IO strategies.

Emerging players

  • Lokon Pharma: Emerging biotech developing oncolytic adenoviruses engineered for tumor-selective replication and immune stimulation. Comparable smaller-scale peer in engineered oncolytic virus immunotherapy.
  • Theriva Biologics: Clinical-stage developer of VCN-01 and other oncolytic adenoviruses for solid tumors. Emerging comparable in the oncolytic virus space with a similar combinatorial IO strategy.

Others

  • Regeneron Pharmaceuticals: Direct partner of SillaJen on the Pexa-Vec + Libtayo RCC combination trial. Relevant as the incumbent checkpoint inhibitor partner validating SillaJen's combination strategy and a potential acquirer/co-developer.

Market position

Strengths5 records

Weaknesses4 records

Competitive moat2 records

Key risks7 records

Key highlights7 records

Customer concentration

SillaJen compliance and trust

Trust signal

Compliance1 record

SillaJen financial estimates

Financial estimate

Revenue estimate

Valuation estimate

SillaJen leadership team

Management profile

Number of profiles

Profiles7 records

SillaJen subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

SillaJen funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

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

SillaJen M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about SillaJen

What does SillaJen do?

SillaJen is a clinical-stage biopharmaceutical company developing engineered oncolytic immunotherapies that selectively infect, replicate in, and destroy cancer cells while stimulating anti-tumor immune response. Core assets include Pexa-Vec (JX-594) in Phase 3 (PHOCUS) for liver cancer and Phase 2 for renal cell carcinoma, BAL0891 (a first-in-class dual TTK/PLK1 inhibitor) in Phase 1, and the SJ-600 series of next-generation oncolytic vaccinia viruses engineered for systemic intravenous delivery with complement evasion capability. The company operates through licensing and co-development partnerships with pharmaceutical companies rather than direct product sales.

Is SillaJen a public or private company?

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

When was SillaJen founded?

SillaJen was founded in 2016. It employs 51 to 100 people.

Where is SillaJen based?

SillaJen is headquartered in San Francisco, United States, in the North America region.

How does SillaJen make money?

Two revenue lines are on record. Licensing and Partnership Revenue is the primary driver. The others are revenue Growth Post-Acquisition.

Who are SillaJen's main competitors?

Direct peers on record are Replimune, Transgene, Oncolytics Biotech and Genelux Corporation. Broad incumbents are Merck & Co., Bristol-Myers Squibb and Amgen. Emerging players are Lokon Pharma and Theriva Biologics. Regeneron Pharmaceuticals is listed as an others.

Does SillaJen have an API?

No public API is recorded for SillaJen.

What industry is SillaJen in?

SillaJen's product category is Oncolytic Immunotherapy. Its primary akta.pro industry code is HLAAAEAB, Therapeutic Vaccines (cancer, chronic infection immunotherapy), with a secondary code of HLAAACAF, Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches). Its NAICS code is 541714 and its SIC code is 2836.

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Live signals
NaverSillajen’s Two CEOs Aim to Redefine the Future With New TechnologiesSillajen's co-CEOs said the company has entered a new growth stage, developing BAL0891 and the SJ-600 oncolytic virus platform. The drug is in clinical trials for solid tumors and AML, and the company expects Woosung Pharmaceutical revenue to exceed $6.7 million. It plans to focus on licensing BAL0891 and expanding its pipeline through SJ-600.NaverHow SJ-607’s Antibody-Evasion Technology Could Revolutionize Cancer TreatmentSillaJen registered a domestic patent for its SJ-607 technology, which enables oncolytic viruses to evade neutralizing antibodies. The platform aims to allow repeated intravenous administration, with the SJ-600 series undergoing process development and toxicity testing. The company plans to incorporate additional anti-cancer agents to enhance efficacy.SedailyKOSDAQ Delisting Rules Tighten, Driving Defensive M&A SurgeThe Korean government has tightened KOSDAQ delisting rules by raising the market capitalization threshold from 15 billion won to 20 billion won and phasing in a revenue threshold increase from 3 billion won to 10 billion won by 2029, driving a surge in defensive M&A among listed SMEs seeking to scale up. The number of companies delisted from KOSDAQ jumped from 8 in 2023 to 38 in 2025, with biotech firm SillaJen and English education firm Gold & S citing significant revenue growth following acquisitions. Elice Group, a modular data center company, is preparing to list on KOSDAQ with a valuation approaching 1 trillion won, supported by strategic investment from Dongkuk Holdings and GS Ventures.GenengnewsTop 10 Organoid CompaniesThe FDA approved the first investigational new drug application supported solely by human vascularized organoid-based combination studies, enabling South Korea-based SillaJen to begin clinical trials for its oncolytic virus combination therapy, marking a regulatory shift away from traditional animal testing under the FDA Modernization Act 2.0. The global organoids market is projected to nearly triple from $1.20 billion last year to $3.29 billion by 2031, with top public companies including Thermo Fisher Scientific ($10.374 billion), Merck KGaA ($10.348 billion), and Danaher ($7.334 billion) leading in revenues. The article ranks the top five public and private organoid companies by revenue or capital raised, highlighting strategic partnerships, acquisitions, and platform launches across the sector.Investing.comOSR Holdings discloses talks on SillaJen stake and Pexa-Vec licensing By Investing.comOSR Holdings disclosed that its subsidiary Vaximm AG is engaged in ongoing but non-binding discussions with South Korea-based SillaJen regarding a potential licensing arrangement for Pexa-Vec, a clinical-stage oncolytic immunotherapy being investigated for renal cell carcinoma. The company also revealed preliminary exploratory discussions about acquiring approximately 16% of SillaJen's outstanding common shares, though no agreement on deal structure, terms, or financing has been reached. OSR Holdings, which has a market capitalization of $12.1 million and whose stock is down 67% over the past year, also received a 180-day extension from Nasdaq to meet the minimum $1.00 bid price requirement for continued listing by August 31, 2026.Investing.comOSR Holdings discloses talks on SillaJen stake and Pexa-Vec licensing By Investing.comOSR Holdings disclosed that its subsidiary Vaximm AG is in ongoing but non-binding discussions with South Korean biopharmaceutical company SillaJen regarding a potential licensing arrangement for Pexa-Vec, a clinical-stage oncolytic immunotherapy being investigated for renal cell carcinoma. The company also reported preliminary discussions about acquiring approximately 16% of SillaJen's outstanding common shares, with no agreement on deal structure, terms, or financing in place. OSR Holdings, with a market cap of just $12.1 million, also received a 180-day Nasdaq extension until August 31, 2026 to meet the minimum $1.00 bid price requirement for continued listing.FierceBiotechFirst FDA IND Milestone Achieved Using Human Vascularized Organoid Efficacy DataQureator Inc. announced that its proprietary vascularized tumor immune microenvironment model (vTIME) enabled SillaJen to secure FDA approval for an Investigational New Drug application for a combination cancer therapy. This marks the world's first FDA IND approval based solely on human vascularized organoid efficacy data, bypassing traditional animal testing under the FDA Modernization Act 2.0. The milestone also received regulatory recognition from Korea's Ministry of Food and Drug Safety, reinforcing the shift toward human-relevant preclinical models.PR NewswireOSR Holdings and SillaJen have entered into a Memorandum of Understanding to collaboratively pursue the development of innovative therapeutics and enter the U.S. marketOSR Holdings, a South Korean global healthcare holding company, and SillaJen, a Kosdaq-listed biotech firm specializing in immuno-oncology, have signed a memorandum of understanding to collaborate on developing innovative therapeutics and entering the U.S. market. The partnership aims to create synergies between OSR Holdings' "hub-and-spoke" business model and SillaJen's pipeline including the GEEV® anti-cancer virus platform and SJ-600 series. SillaJen expects the collaboration to provide an opportunity to present its exceptional pipeline in the United States, the world's largest pharmaceutical market.PR NewswireSillaJen Defending Position Relating to Recent Sale of Stock by EmployeeSillaJen, Inc. is cooperating with the Joint Securities Crime Investigation Division of the Southern Seoul Prosecutors Office over allegations that an employee sold shares using undisclosed information, which the company denies as a routine July trade made during an open trading window. The company clarified that no employees had access to interim futility analysis results from the Phase 3 PHOCUS trial for advanced liver cancer prior to the August 1 IDMC meeting, after which the trial was discontinued. CEO Dr. Eun Sang Moon reaffirmed the company's commitment to cooperating with authorities and continuing the study of Pexa-Vec for difficult-to-treat cancers.PR NewswireSillaJen Announces First Patient Enrolled in Part 2 of Renal Cell Carcinoma Trial with Pexa-Vec in Combination with Regeneron's Libtayo® (cemiplimab-rwlc)SillaJen announced the first patient has been enrolled in Part 2 of the JX594-REN026 Phase 1b clinical trial evaluating Pexa-Vec in combination with Libtayo® (cemiplimab-rwlc) for treating renal cell carcinoma. Part 1 of the dose-escalation phase was completed in March 2019 without significant safety concerns, with initial Part 2 enrollment occurring in South Korea and planned expansion to sites in the United States and Australia. SillaJen is collaborating with Regeneron on this trial, which aims to assess the safety and efficacy of the combination therapy alongside investigating immune modulating potential through blood and tissue biomarkers.