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SalubrisBio

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uuid0000xtg

Namestring
SalubrisBio
Legal namestring
Salubris Biotherapeutics, Inc.
Websiteurl
salubrisbio.com
Company typeenum
Private
Founded yearint
2016
Descriptiontext

SalubrisBio (legal name Salubris Biotherapeutics, Inc.) is a clinical-stage biotechnology company founded in August 2016 as a wholly-owned subsidiary of Shenzhen Salubris Pharmaceuticals Co., Ltd., a China-based pharmaceutical company. The company is headquartered in Gaithersburg, Maryland, with an additional office at the Cambridge Innovation Center in Cambridge, Massachusetts, and operates with 11–50 employees. Its sole investor and parent has provided over $100 million in funding across three tranches ($32M in March 2022, $35M in March 2023, and $35M in April 2024).

The company is developing a portfolio of three clinical-stage complex biologic therapeutics. JK07 is a recombinant antibody fusion protein composed of an NRG-1 polypeptide fused to a fully human IgG1 monoclonal antibody targeting ErbB3; it selectively stimulates the ErbB4 pathway while blocking HER3 to treat heart failure with reduced and preserved ejection fraction (HFrEF and HFpEF), and is currently in Phase 2 (RENEU-HF trial) with expansion into Group 2 pulmonary hypertension (RENEU-PH). JK06 is a first-in-class quadrivalent, biparatopic antibody-drug conjugate targeting the 5T4 oncofetal antigen with an MMAE payload, currently in Phase 1/2 for solid tumors. JK08 is a recombinant fusion combining a CTLA-4-specific antibody with an IL-15 fusion domain to combine checkpoint inhibition with NK cell activation in solid tumors, also in Phase 1/2.

SalubrisBio has no marketed products and generates no commercial revenue. Its business model is preclinical and clinical-stage R&D, funded entirely by corporate parent equity contributions, with value creation expected through eventual commercialization, partnership, or acquisition of its novel biologic assets. Clinical trial operations span the United States and Europe (UK, Belgium, Spain) via collaborations with academic centers including Cleveland Clinic, Jules Bordet Institute, Vall d'Hebron Institute of Oncology, and NEXT Oncology. The company addresses two large patient populations—approximately 6.7 million Americans and 64 million people worldwide living with heart failure, plus broad solid tumor populations expressing 5T4—with disease-modifying potential in indications where current standard of care remains inadequate.

Short descriptiontext

SalubrisBio is a clinical-stage biotechnology company developing novel antibody fusion proteins and antibody-drug conjugates for heart failure (JK07) and solid tumors (JK06, JK08). It is a wholly-owned subsidiary of Shenzhen Salubris Pharmaceuticals.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersGaithersburg, United States
HQ citystring
Gaithersburg
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
antibody therapeutics, antibody-drug conjugates, fusion proteins, cardiovascular biologics, oncology biologics
Industry3 codes
1Fusion Proteins & Fc-Engineered Biologics
CodeHLAAAAADPrimaryYes
2Bispecific & Multispecific Antibodies
CodeHLAAAAAFPrimaryNo
3Cardiology & Vascular Specialty Pharmaceuticals
CodeHLAIACAGPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Clinical-stage Biopharmaceuticals
Social media profiles1 record
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 components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

SalubrisBio is a clinical-stage biotechnology company developing a portfolio of novel antibody fusion proteins and antibody-drug conjugates (ADCs) for cardiovascular disease and oncology. Its pipeline includes JK07, an NRG-1/ErbB4 selective agonist antibody fusion protein in Phase 2 for heart failure; JK08, an IL-15/CTLA-4 antibody fusion in Phase 1/2 for solid tumors; and JK06, a first-in-class 5T4-targeted biparatopic ADC in Phase 1/2 for solid tumors. The company has no commercially marketed products; all candidates are investigational biologics in active clinical development.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • JK07 Phase 1b: 49% average relative improvement in ejection fraction at 6 months following single dose at 0.09 mg/kg
+3 more records
Product overview1 text field

SalubrisBio is a clinical-stage biotechnology company developing a portfolio of novel complex biologic therapeutics targeting cardiovascular disease and oncology. The company's pipeline consists of three clinical-stage assets: JK07 is an NRG1-ErbB3 antibody fusion protein for heart failure (HFrEF and HFpEF), JK08 is an IL15-CTLA4 antibody fusion for solid tumors, and JK06 is a 5T4-targeted biparatopic ADC for solid tumors. JK07 is the company's lead cardiovascular candidate in Phase 2, while JK06 and JK08 are in Phase 1/2 oncology trials.

Product and service3 records
1JK07
CategoryCardiovascular biologic therapeutic
Description

JK07 is a recombinant antibody fusion protein consisting of an active polypeptide fragment of neuregulin-1 (NRG-1) and a fully human IgG1 monoclonal antibody targeting ErbB3. It selectively stimulates the ErbB4 pathway while blocking the HER3/ErbB3 pathway to widen the therapeutic window. JK07 is being developed for heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF), and is in Phase 2 (RENEU-HF) and Phase 2a (RENEU-PH) clinical trials.

2JK08
CategoryOncology immune-engaging biologic therapeutic
Description

JK08 is a recombinant fusion protein consisting of a CTLA-4-specific antibody and an IL-15 fusion domain. It is designed to synergistically combine CTLA-4 targeting with IL-15 immune stimulation for the treatment of solid tumors, with the goal of depleting T-regulatory cells and reversing immunosuppression. JK08 has shown dose-dependent pharmacodynamic activity with NK and CD8+ T cell induction and is in Phase 1/2 clinical development.

3JK06
CategoryOncology antibody-drug conjugate (ADC) therapeutic
Description

JK06 is a first-in-class quadrivalent, biparatopic antibody-drug conjugate (ADC) that selectively targets 5T4—an oncofetal protein overexpressed in lung, breast, renal, and genitourinary cancers—with an MMAE payload. JK06 has demonstrated picomolar affinity for 5T4 and rapid internalization due to its biparatopic design, and is in Phase 1/2 clinical trials for solid tumors including non-small cell lung cancer and breast cancer. As of May 2026, 173 patients had been treated across the JK06 Phase 1/2 study with no Grade 4 or 5 TRAEs reported.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeOthers
Description

Cleveland Clinic serves as a clinical research site for JK07 heart failure trials. Dr. W.H. Wilson Tang, Research Director for the Section of Heart Failure and Cardiac Transplant Medicine at Cleveland Clinic, is a lead investigator and has presented clinical data from JK07 trials.

2Jules Bordet Institute
Strategic tierCoreTypeOthers
Description

Dr. Nuria Kotecki from Jules Bordet Institute in Brussels serves as an investigator for JK06 clinical trials and has provided expert commentary on the 5T4 target and therapeutic potential.

salubrisbio.com
Strategic tierCoreTypeOthers
Description

Dr. Omar Saavedra from VHIO in Barcelona presented JK06 expansion cohort data at AACR 2026 and serves as an investigator in the JK06 Phase 1/2 study.

4New Experimental Therapeutics (NEXT) Oncology
Strategic tierMinorTypeOthers
Description

Dr. Omar Saavedra from NEXT Oncology at Hospital Universitario Quironsalud Barcelona serves as an investigator and presenter for JK06 ASCO 2026 data.

salubrisbio.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global pharmaceutical company with major cardiovascular (Farxiga/Dapagliflozin for HF) and oncology ADC franchises (Enhertu with Daiichi). Comparable to SalubrisBio's combined HF and ADC oncology focus; multiple SalubrisBio executives came from MedImmune/AstraZeneca.

TypeDirect peer
Description

Clinical-stage biotech developing multispecific antibody therapeutics including Azymetric bispecific platform and zanidatamab. Comparable to SalubrisBio's multispecific antibody-fusion approach and oncology pipeline breadth.

TypeDirect peer
Description

Clinical-stage oncology company developing bispecific and multispecific antibodies with proprietary PowerBody and SAFEbody platforms. Comparable to JK06 and JK08 given similar multispecific antibody engineering approach and solid tumor focus.

TypeEmerging player
Description

Clinical-stage gene therapy company focused on cardiovascular diseases including Friedreich's ataxia cardiomyopathy and other cardiac genetic disorders. Comparable emerging cardiovascular biotech with similar biologic modality and unmet need focus.

TypeDirect peer
Description

Clinical-stage cardiovascular company developing cardiac myosin activators (e.g., omecamtiv mecarbil, aficamten) for heart failure. Most directly comparable to SalubrisBio's JK07 heart failure program, with similar Phase 2/3 development stage and patient population focus.

TypeBroad incumbent
Description

Global pharmaceutical company with significant cardiovascular and oncology biologics portfolios (e.g., Sotyktu, Opdivo). SalubrisBio's CMO previously led Sotyktu development at BMS; comparable as broad incumbent in the same therapeutic categories where SalubrisBio's assets compete.

TypeDirect peer
Description

Genetic medicines company developing cardiac gene therapies and regenerative approaches for heart failure and cardiomyopathies. Directly comparable to JK07 as another clinical-stage company targeting disease modification in HFrEF/HFpEF.

TypeDirect peer
Description

Clinical-stage ADC company developing Dolasynthen and Immunosynthen platforms across solid tumors including NSCLC and breast cancer. Most comparable to JK06 given overlapping oncology indications (NSCLC, breast cancer) and ADC modality.

TypeDirect peer
Description

Clinical-stage immuno-oncology company developing T cell engager (TCE) bispecific antibodies. Comparable to SalubrisBio's JK08 immunocytokine/dual-mechanism oncology biologics in targeting tumors with engineered multispecific antibody constructs.

TypeDirect peer
Description

Clinical-stage immuno-oncology company developing immune-stimulating antibody conjugates (ISACs), a bispecific/multispecific ADC platform targeting tumor antigens with payload + immune stimulation. Directly comparable to SalubrisBio's JK06 biparatopic ADC strategy.

Market position
Strengths4 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

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Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

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

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles8 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

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&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 →

SalubrisBio

Clinical-stage Biopharmaceuticalssalubrisbio.com

SalubrisBio is a clinical-stage biotechnology company developing novel antibody fusion proteins and antibody-drug conjugates for heart failure (JK07) and solid tumors (JK06, JK08). It is a wholly-owned subsidiary of Shenzhen Salubris Pharmaceuticals.

What SalubrisBio does

SalubrisBio (legal name Salubris Biotherapeutics, Inc.) is a clinical-stage biotechnology company founded in August 2016 as a wholly-owned subsidiary of Shenzhen Salubris Pharmaceuticals Co., Ltd., a China-based pharmaceutical company. The company is headquartered in Gaithersburg, Maryland, with an additional office at the Cambridge Innovation Center in Cambridge, Massachusetts, and operates with 11–50 employees. Its sole investor and parent has provided over $100 million in funding across three tranches ($32M in March 2022, $35M in March 2023, and $35M in April 2024).

The company is developing a portfolio of three clinical-stage complex biologic therapeutics. JK07 is a recombinant antibody fusion protein composed of an NRG-1 polypeptide fused to a fully human IgG1 monoclonal antibody targeting ErbB3; it selectively stimulates the ErbB4 pathway while blocking HER3 to treat heart failure with reduced and preserved ejection fraction (HFrEF and HFpEF), and is currently in Phase 2 (RENEU-HF trial) with expansion into Group 2 pulmonary hypertension (RENEU-PH). JK06 is a first-in-class quadrivalent, biparatopic antibody-drug conjugate targeting the 5T4 oncofetal antigen with an MMAE payload, currently in Phase 1/2 for solid tumors. JK08 is a recombinant fusion combining a CTLA-4-specific antibody with an IL-15 fusion domain to combine checkpoint inhibition with NK cell activation in solid tumors, also in Phase 1/2.

SalubrisBio has no marketed products and generates no commercial revenue. Its business model is preclinical and clinical-stage R&D, funded entirely by corporate parent equity contributions, with value creation expected through eventual commercialization, partnership, or acquisition of its novel biologic assets. Clinical trial operations span the United States and Europe (UK, Belgium, Spain) via collaborations with academic centers including Cleveland Clinic, Jules Bordet Institute, Vall d'Hebron Institute of Oncology, and NEXT Oncology. The company addresses two large patient populations—approximately 6.7 million Americans and 64 million people worldwide living with heart failure, plus broad solid tumor populations expressing 5T4—with disease-modifying potential in indications where current standard of care remains inadequate.

SalubrisBio firmographics

Firmographics
Name
SalubrisBio
Legal name
Salubris Biotherapeutics, Inc.
Website
https://salubrisbio.com
Company type
Private
Founded year
2016
Operating status
Operating
Headcount range
11–50 employees
Short description
SalubrisBio is a clinical-stage biotechnology company developing novel antibody fusion proteins and antibody-drug conjugates for heart failure (JK07) and solid tumors (JK06, JK08). It is a wholly-owned subsidiary of Shenzhen Salubris Pharmaceuticals.
Ownership category
akta.pro rank

SalubrisBio industry classification

Industry
Product category
Clinical-stage Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Fusion Proteins & Fc-Engineered Biologics (HLAAAAAD)
akta.pro secondary industries
Bispecific & Multispecific Antibodies (HLAAAAAF), Cardiology & Vascular Specialty Pharmaceuticals (HLAIACAG)

Keywords

  • Antibody therapeutics
  • Antibody-drug conjugates
  • Fusion proteins
  • Cardiovascular biologics
  • Oncology biologics

Where SalubrisBio is headquartered

Location

Headquarters

HQ city
Gaithersburg
HQ country
United States
HQ region
North America

Offices2 records

Markets served

SalubrisBio business model

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

Distribution channels1 record

Marketing channels4 records

SalubrisBio product offering

Product offering

Core offering

SalubrisBio is a clinical-stage biotechnology company developing a portfolio of novel antibody fusion proteins and antibody-drug conjugates (ADCs) for cardiovascular disease and oncology. Its pipeline includes JK07, an NRG-1/ErbB4 selective agonist antibody fusion protein in Phase 2 for heart failure; JK08, an IL-15/CTLA-4 antibody fusion in Phase 1/2 for solid tumors; and JK06, a first-in-class 5T4-targeted biparatopic ADC in Phase 1/2 for solid tumors. The company has no commercially marketed products; all candidates are investigational biologics in active clinical development.

Product overview

SalubrisBio is a clinical-stage biotechnology company developing a portfolio of novel complex biologic therapeutics targeting cardiovascular disease and oncology. The company's pipeline consists of three clinical-stage assets: JK07 is an NRG1-ErbB3 antibody fusion protein for heart failure (HFrEF and HFpEF), JK08 is an IL15-CTLA4 antibody fusion for solid tumors, and JK06 is a 5T4-targeted biparatopic ADC for solid tumors. JK07 is the company's lead cardiovascular candidate in Phase 2, while JK06 and JK08 are in Phase 1/2 oncology trials.

Differentiator

Problem solved

Functional benefit

Products and services

  • JK07 JK07 is a recombinant antibody fusion protein consisting of an active polypeptide fragment of neuregulin-1 (NRG-1) and a fully human IgG1 monoclonal antibody targeting ErbB3. It selectively stimulates the ErbB4 pathway while blocking the HER3/ErbB3 pathway to widen the therapeutic window. JK07 is being developed for heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF), and is in Phase 2 (RENEU-HF) and Phase 2a (RENEU-PH) clinical trials.
  • JK08 JK08 is a recombinant fusion protein consisting of a CTLA-4-specific antibody and an IL-15 fusion domain. It is designed to synergistically combine CTLA-4 targeting with IL-15 immune stimulation for the treatment of solid tumors, with the goal of depleting T-regulatory cells and reversing immunosuppression. JK08 has shown dose-dependent pharmacodynamic activity with NK and CD8+ T cell induction and is in Phase 1/2 clinical development.
  • JK06 JK06 is a first-in-class quadrivalent, biparatopic antibody-drug conjugate (ADC) that selectively targets 5T4—an oncofetal protein overexpressed in lung, breast, renal, and genitourinary cancers—with an MMAE payload. JK06 has demonstrated picomolar affinity for 5T4 and rapid internalization due to its biparatopic design, and is in Phase 1/2 clinical trials for solid tumors including non-small cell lung cancer and breast cancer. As of May 2026, 173 patients had been treated across the JK06 Phase 1/2 study with no Grade 4 or 5 TRAEs reported.

Quantifiable outcome

  • JK07 Phase 1b: 49% average relative improvement in ejection fraction at 6 months following single dose at 0.09 mg/kg
  • +3 more outcomes

Companies that use SalubrisBio

Customer profile

Segments2 records

Ideal customer profiles2 records

SalubrisBio technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

SalubrisBio partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Cleveland CliniccoreOthersCleveland Clinic serves as a clinical research site for JK07 heart failure trials. Dr. W.H. Wilson Tang, Research Director for the Section of Heart Failure and Cardiac Transplant Medicine at Cleveland Clinic, is a lead investigator and has presented clinical data from JK07 trials.
  • Jules Bordet InstitutecoreOthersDr. Nuria Kotecki from Jules Bordet Institute in Brussels serves as an investigator for JK06 clinical trials and has provided expert commentary on the 5T4 target and therapeutic potential.
  • Vall d'Hebron Institute of Oncology (VHIO)coreOthersDr. Omar Saavedra from VHIO in Barcelona presented JK06 expansion cohort data at AACR 2026 and serves as an investigator in the JK06 Phase 1/2 study.
  • New Experimental Therapeutics (NEXT) OncologyminorOthersDr. Omar Saavedra from NEXT Oncology at Hospital Universitario Quironsalud Barcelona serves as an investigator and presenter for JK06 ASCO 2026 data.

Scale indicators8 records

Recent moves6 records

Expansion highlights5 records

SalubrisBio competitors and assessment

Company assessment

Broad incumbents

  • AstraZeneca: Global pharmaceutical company with major cardiovascular (Farxiga/Dapagliflozin for HF) and oncology ADC franchises (Enhertu with Daiichi). Comparable to SalubrisBio's combined HF and ADC oncology focus; multiple SalubrisBio executives came from MedImmune/AstraZeneca.
  • Bristol Myers Squibb: Global pharmaceutical company with significant cardiovascular and oncology biologics portfolios (e.g., Sotyktu, Opdivo). SalubrisBio's CMO previously led Sotyktu development at BMS; comparable as broad incumbent in the same therapeutic categories where SalubrisBio's assets compete.

Direct peers

  • Zymeworks: Clinical-stage biotech developing multispecific antibody therapeutics including Azymetric bispecific platform and zanidatamab. Comparable to SalubrisBio's multispecific antibody-fusion approach and oncology pipeline breadth.
  • Adagene: Clinical-stage oncology company developing bispecific and multispecific antibodies with proprietary PowerBody and SAFEbody platforms. Comparable to JK06 and JK08 given similar multispecific antibody engineering approach and solid tumor focus.
  • Cytokinetics: Clinical-stage cardiovascular company developing cardiac myosin activators (e.g., omecamtiv mecarbil, aficamten) for heart failure. Most directly comparable to SalubrisBio's JK07 heart failure program, with similar Phase 2/3 development stage and patient population focus.
  • Tenaya Therapeutics: Genetic medicines company developing cardiac gene therapies and regenerative approaches for heart failure and cardiomyopathies. Directly comparable to JK07 as another clinical-stage company targeting disease modification in HFrEF/HFpEF.
  • Mersana Therapeutics: Clinical-stage ADC company developing Dolasynthen and Immunosynthen platforms across solid tumors including NSCLC and breast cancer. Most comparable to JK06 given overlapping oncology indications (NSCLC, breast cancer) and ADC modality.
  • Janux Therapeutics: Clinical-stage immuno-oncology company developing T cell engager (TCE) bispecific antibodies. Comparable to SalubrisBio's JK08 immunocytokine/dual-mechanism oncology biologics in targeting tumors with engineered multispecific antibody constructs.
  • Bolt Biotherapeutics: Clinical-stage immuno-oncology company developing immune-stimulating antibody conjugates (ISACs), a bispecific/multispecific ADC platform targeting tumor antigens with payload + immune stimulation. Directly comparable to SalubrisBio's JK06 biparatopic ADC strategy.

Emerging players

  • Lexeo Therapeutics: Clinical-stage gene therapy company focused on cardiovascular diseases including Friedreich's ataxia cardiomyopathy and other cardiac genetic disorders. Comparable emerging cardiovascular biotech with similar biologic modality and unmet need focus.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

SalubrisBio social profiles

Digital presence

SalubrisBio financial estimates

Financial estimate

Revenue estimate

Valuation estimate

SalubrisBio leadership team

Management profile

Number of profiles

Profiles8 records

SalubrisBio funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors1 record

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

SalubrisBio 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 SalubrisBio

What does SalubrisBio do?

SalubrisBio is a clinical-stage biotechnology company developing a portfolio of novel antibody fusion proteins and antibody-drug conjugates (ADCs) for cardiovascular disease and oncology. Its pipeline includes JK07, an NRG-1/ErbB4 selective agonist antibody fusion protein in Phase 2 for heart failure; JK08, an IL-15/CTLA-4 antibody fusion in Phase 1/2 for solid tumors; and JK06, a first-in-class 5T4-targeted biparatopic ADC in Phase 1/2 for solid tumors. The company has no commercially marketed products; all candidates are investigational biologics in active clinical development.

Is SalubrisBio a public or private company?

SalubrisBio is a private company. It is classified as corporate owned and is currently operating.

When was SalubrisBio founded?

SalubrisBio was founded in 2016. It employs 11 to 50 people.

Where is SalubrisBio based?

SalubrisBio is headquartered in Gaithersburg, United States, in the North America region.

Who are SalubrisBio's main competitors?

Broad incumbents on record are AstraZeneca and Bristol Myers Squibb. Direct peers are Zymeworks, Adagene, Cytokinetics, Tenaya Therapeutics, Mersana Therapeutics, Janux Therapeutics and Bolt Biotherapeutics. Lexeo Therapeutics is listed as an emerging player.

Does SalubrisBio have an API?

No public API is recorded for SalubrisBio.

What industry is SalubrisBio in?

SalubrisBio's product category is Clinical-stage Biopharmaceuticals. Its primary akta.pro industry code is HLAAAAAD, Fusion Proteins & Fc-Engineered Biologics, with a secondary code of HLAAAAAF, Bispecific & Multispecific Antibodies. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
BioSpaceSalubris Biotherapeutics Announces Updated Phase 1/2 Data for JK06, a 5T4-Targeted Antibody Drug Conjugate, at the 2026 American Society of Clinical Oncology Annual MeetingSalubris Biotherapeutics presented updated Phase 1/2 data for JK06, a 5T4-targeted ADC, at the 2026 ASCO meeting. The data showed a 50% objective response rate in squamous NSCLC at 4.5 mg/kg and a 94% disease control rate across 173 patients. The company plans to advance JK06 into additional monotherapy and combination expansions.JiemianXintai announced the progress of the JK06 overseas clinical trial.Xintai announced that its subsidiary Salubris Bio presented phase 1/2 expanded cohort data for JK06 at AACR 2026, showing safety and efficacy in unresectable NSCLC and breast cancer. JK06 is a 5T4-targeting ADC with MMAE payload, and the European phase I/II trial is advancing into dose-expansion with plans to increase monotherapy and evaluate combination therapies.Business Wire BlogSalubris Biotherapeutics Presents Phase 1/2 Dose Escalation and Expansion Cohort Data for JK06, 5T4-Targeted Antibody Drug Conjugate, at the American Association for Cancer Research Annual MeetingSalubris Biotherapeutics presented Phase 1/2 data for JK06, a 5T4-targeted ADC, at AACR 2026. Among 112 patients, 10 of 38 NSCLC patients and 5 of 19 breast cancer patients achieved partial responses (ORR 26% each). The study continues with expansion cohorts and combination therapy evaluation.PharmiWeb.comSalubris Biotherapeutics Announces Dose Escalation Data for JK06, a 5T4-Targeted Antibody Drug Conjugate, at the European Society for Medical Oncology 2025 CongressSalubris Biotherapeutics announced dose escalation data from the Phase 1/2 study of JK06, a 5T4-targeted antibody drug conjugate, showing 6 confirmed partial responses among 29 evaluable patients with advanced relapsed/refractory solid tumors, including a 38% objective response rate in non-small cell lung cancer and 1 partial response in breast cancer. The trial enrolled 34 patients in Europe across five dose levels (1.5-8.0 mg/kg), with 83% having received three or more prior lines of therapy, and demonstrated a favorable safety profile with predominantly low-grade toxicities. The company is proceeding with expansion cohorts in NSCLC and breast cancer to determine the recommended Phase 2 dose.Business Wire BlogSalubris Biotherapeutics Announces Dose Escalation Data for JK06, a 5T4-Targeted Antibody Drug Conjugate, at the European Society for Medical Oncology 2025 CongressSalubris Biotherapeutics announced positive dose escalation data from a Phase 1/2 study of JK06, a 5T4-targeted antibody drug conjugate, showing 6 confirmed partial responses (21%) among 29 evaluable patients with advanced relapsed/refractory solid tumors, including an objective response rate of 38% in non-small cell lung cancer and 1 partial response in breast cancer. The drug demonstrated a favorable safety profile with predominantly low-grade manageable toxicities across five dose levels (1.5-8.0 mg/kg). The company plans to advance the study into dose expansion cohorts in NSCLC and breast cancer to determine the recommended Phase 2 dose.Pulse 2.0Salubris Biotherapeutics: $35 Million Secured To Fund Development Of Biologic TherapeuticsSalubris Biotherapeutics raised $35 million to fund R&D of its biologic therapeutics. The company reported progress on JK07, JK08, and JK06, including enrollment of 282 subjects in the JK07 Phase 2 trial and first-patient dosing in the JK08 study. It plans to report additional JK08 data in the second half of 2024.Business Wire BlogSalubris Biotherapeutics Announces $35 Million in Financing and Provides Pipeline Progress UpdateSalubris Biotherapeutics announced a $35 million capital infusion to fund the research and development of its clinical and pre-clinical programs, including updates on JK07 for heart failure, JK08 for solid tumors, and JK06. The company reported enrolling the first patient in the Phase 2 trial for JK07 and dosing the first patient in the cohort expansion phase for JK08. These developments position SalubrisBio for multiple inflection points as it advances its pipeline of novel biologic therapeutics.BioSpaceSalubris Biotherapeutics Announces $35 Million in Financing and Provides Pipeline Progress UpdateSalubris Biotherapeutics announced a $35 million capital infusion to fund its research and development pipeline, including the clinical-stage biologic JK07 for heart failure. The company also reported that the first patient has been enrolled in the Phase 2 RENEU-HF trial for JK07 and filed a Clinical Trial Application for its first-in-class biparatopic ADC, JK06.MedtechalertSalubris Biotherapeutics Announces $35 Million Financing to Advance Development Activities and Provides Pipeline UpdatesSalubris Biotherapeutics secured $35 million in financing from Shenzhen Salubris Pharmaceuticals to advance its drug pipeline, including the initiation of a Phase 2 study for lead candidate JK07 in heart failure. The funding will also support ongoing trials for JK07 in HFpEF and JK08 in solid tumors, as well as the launch of the first neurology clinical trial for JK07.Business Wire BlogSalubris Biotherapeutics Announces $35 Million Financing to Advance Development Activities and Provides Pipeline UpdatesSalubris Biotherapeutics, Inc. announced that it has secured $35 million in financing from Shenzhen Salubris Pharmaceuticals Co., Ltd. to support various clinical trials, including the initiation of a Phase 2 study for its lead candidate JK07 in heart failure. The funding will also aid in advancing additional therapeutic candidates within their pipeline and associated clinical studies throughout 2023.