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Arch Biopartners

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uuid00051aj

Namestring
Arch Biopartners
Legal namestring
Arch Biopartners Inc.
Company typeenum
Public
Founded yearint
2010
Descriptiontext

Arch Biopartners is a clinical-stage biopharmaceutical company founded in 2010 and headquartered in Toronto, Canada, listed on the TSX Venture Exchange (ARCH) and OTCQB (ACHFF). The company develops novel therapeutics targeting acute kidney injury (AKI) and chronic kidney disease (CKD), anchored on the DPEP-1 (dipeptidase-1) inhibition pathway. Its scientific foundation draws on research from the University of Calgary's Snyder Institute, where Co-Founder and CSO Dr. Daniel Muruve leads the underlying biology. The company operates with a small team of 1-10 employees and has approximately 67.9 million common shares outstanding as of April 2026.

Arch's pipeline includes two Phase II-stage drug candidates: LSALT peptide (also referred to as Metablok), a proprietary DPEP-1 inhibitor being evaluated for cardiac surgery-associated acute kidney injury (CS-AKI), and cilastatin, a repurposed drug licensed from Telara Pharma (Spain) in April 2021 that is being evaluated in the 700-patient PONTiAK Phase II trial for toxin- and drug-induced AKI. In September 2025, the company expanded into chronic kidney disease through the acquisition of Lipdro Therapeutics Inc., adding a pre-clinical platform targeting IL-32. The platform is supported by composition-of-matter and method-of-use patents covering LSALT peptide, the licensed cilastatin rights, and the newly acquired IL-32 CKD IP.

The company is pre-revenue and funds operations through a combination of small non-brokered private placements, Canadian federal grants (notably CAD $4M from NRC IRAP in 2023 and CAD $750K from CIHR in 2021), and equity issuance. Clinical execution is currently distributed across nine trial sites globally, four in Canada and five international. The business model assumes future monetization through licensing, partnership, or direct commercialization of assets following Phase II/III readouts, rather than near-term product sales. Governance was strengthened in 2024-2025 by the appointment of Dr. Patrick Vink as Chairman, bringing senior commercial drug-development experience from Cubist Pharmaceuticals and Merck.

Short descriptiontext

Arch Biopartners is a Toronto-based, pre-revenue clinical-stage biotech developing DPEP-1 inhibiting therapeutics (LSALT peptide, cilastatin) for acute kidney injury and a recently acquired IL-32 platform for chronic kidney disease, conducting Phase II trials across nine global sites.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersToronto, Canada
HQ citystring
Toronto
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
acute kidney injury therapeutics, chronic kidney disease treatments, DPEP-1 inhibitor drugs, clinical stage biotech, anti-inflammatory peptide drugs
Industry5 codes
1Rare Renal & Nephrology Disorder Therapies
CodeHLAIAIAIPrimaryYes
2Nephrology & Urology Pharmaceuticals
CodeHLAIAAAMPrimaryNo
3Nephrology & Urology Specialty Pharmaceuticals
CodeHLAIACAHPrimaryNo
4Engineered Protein Therapeutics (de novo/AI-designed proteins, novel scaffolds)
CodeHLAAAAAJPrimaryNo
5Therapeutic Peptides & Protein/Peptide Biologics
CodeHLAAAAAHPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical and Medicine Manufacturing3254
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Kidney Disease Therapeutics
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Drug Development and Commercialization
TypeOne Time License
Description

Pre-revenue clinical stage biotech company. Revenue will be generated from commercialization of drug candidates LSALT peptide and cilastatin upon regulatory approval. Both drugs target acute kidney injury (AKI), a condition affecting over 10 million people annually in the U.S. and Europe, with an estimated worldwide market over $20 billion USD per year.

archbiopartners.com:443
2Private Placements
TypeLicensing Royalties
Description

The company raises capital through non-brokered private placement offerings of common shares to fund operations and clinical trials. Recent financings include $600,000 CAD (April 2026), $600,000 CAD (November 2025), and $500,000 CAD (November 2025).

archbiopartners.com
3Government Grants and Funding
TypeLicensing Royalties
Description

Non-dilutive funding from government agencies including NRC IRAP ($4 million in 2023) for clinical development activities and CIHR Team Grants ($750,000 in 2021) for pre-clinical and clinical trial design research.

archbiopartners.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Metablok
Description

Brand name for LSALT peptide drug candidate

archbiopartners.com
+1 more record
Core offering1 text field

Arch Biopartners is a clinical-stage therapeutic biotech company developing novel, on-target drug candidates for acute kidney injury (AKI) and chronic kidney disease (CKD). Its portfolio includes two lead DPEP-1 inhibitors in Phase II trials (LSALT peptide / Metablok for cardiac surgery-associated AKI and Cilastatin for toxin-induced AKI), plus a pre-clinical CKD platform targeting IL-32. The company acquires and develops these products and technology for sale to pharmaceutical companies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 74% lower risk of AKI in randomized controlled trials (cilastatin)
+4 more records
Product overview1 text field

Arch Biopartners is a therapeutic biotech company developing a pipeline of novel, on-target drugs for kidney injury and disease. The company's portfolio spans both acute kidney injury (AKI) and chronic kidney disease (CKD) through three main programs: (1) LSALT Peptide (Metablok), a first-in-class DPEP1 inhibitor in Phase II trials for cardiac surgery-associated AKI; (2) Cilastatin, a repurposed DPEP1 inhibitor in Phase II trials targeting toxin-induced AKI; and (3) a pre-clinical CKD Platform targeting IL-32 for chronic kidney disease. The company also holds patents for both LSALT peptide and cilastatin as AKI treatments through the DPEP1 pathway.

Product and service3 records
1LSALT Peptide (Metablok)
CategoryAcute Kidney Injury Drug Candidate
Description

A first-in-class DPEP-1 inhibitor peptide designed to protect the kidneys from ischemia-reperfusion injury during cardiac surgery. Currently in a global Phase II trial (CS-AKI) evaluating its ability to prevent acute kidney injury in patients undergoing on-pump cardiac surgery, with a recruitment target of 240 patients.

2Cilastatin
CategoryAcute Kidney Injury Drug Candidate
Description

A repurposed DPEP-1 inhibitor being evaluated for its ability to block toxic drug uptake into the kidneys and prevent toxin-induced acute kidney injury caused by antibiotics, chemotherapeutics, and contrast agents. Currently in the Phase II PONTiAK trial (700 patients, CIHR/ACT funded).

3CKD Platform (IL-32 Targeting)
CategoryChronic Kidney Disease Drug Platform
Description

A pre-clinical research platform targeting IL-32, a non-classical cytokine directly implicated in diabetic kidney disease, the leading cause of kidney failure worldwide. The platform aims to develop novel, on-target therapeutics for chronic kidney disease based on research linking IL-32 to tubular injury in diabetic kidney disease.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-24
Description

Clinical Trial Agreement enabling Royal Columbian Hospital to begin recruitment for Phase II trial evaluating LSALT peptide for cardiac surgery-associated AKI. Royal Columbian Hospital is the ninth site activated globally and fourth in Canada for the trial.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-11-05
Description

Acquisition completed to strengthen company's position in kidney therapeutics and add breakthrough platform for developing new drugs targeting chronic kidney disease (CKD Platform).

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2021-04-15
Description

Worldwide exclusive license agreement for clinical development and marketing of cilastatin for treatment and prevention of acute kidney injury. Telara Pharma, a spin-off from Hospital General Gregorio Marañón in Madrid, Spain, provides Phase I safety data and established cilastatin drug manufacturing program. Patents unified with Arch's existing patent portfolio.

4Hospital General Gregorio Marañón (Madrid, Spain)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-04-15
Description

Public research hospital whose Nephrology Service (led by Drs. Alberto Tejedor and Alberto Lazaro) discovered the nephroprotective effect of cilastatin, resulting in patents for treatment of kidney damage caused by drugs and sepsis. Spin-off company Telara Pharma created to bring cilastatin to clinical use.

archbiopartners.com
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Core scientific research partner. Scientific team led by Dr. Daniel Muruve (CSO) and Dr. Justin Chun (Principal Scientist, CKD Platform) from the Cumming School of Medicine. Research established DPEP-1 pathway as therapeutic target for kidney inflammation.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Phase II clinical trial site evaluating LSALT peptide for preventing AKI in on-pump cardiac surgery patients. Part of ongoing multi-center trial with recruitment target of 240 patients.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Phase II clinical trial site for LSALT peptide, third Canadian site to recruit patients. Ethics approval received December 2025; commenced patient dosing March 2026.

Recent move7 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 recombinant alkaline phosphatase for acute kidney injury; one of the most direct comparables to Arch's AKI-focused pipeline (acquired by Pfizer in 2022 in a deal valued at ~$1.3B).

TypeDirect peer
Description

Clinical-stage biotech developing RMC-035 (a small protein/peptide) for prevention of cardiac surgery-associated AKI; directly competes with Arch's LSALT peptide in the CS-AKI indication.

TypeEmerging player
Description

Clinical-stage biotech focused on acute and chronic kidney injury with small-molecule and biologic candidates; comparable as a kidney-injury focused developer at similar development stage.

TypeEmerging player
Description

Late-stage clinical and commercial biotech with kidney disease programs (sparsentan/Filspari in IgA nephropathy and FSGS); overlaps with Arch on CKD therapeutics targeting rare kidney disorders.

TypeEmerging player
Description

Clinical-stage nephrology biotech acquired by Novartis for up to ~$3.5B in 2023; pursued IgA nephropathy and other rare kidney diseases, validating big-pharma appetite for kidney assets at Arch's stage.

TypeEmerging player
Description

Commercial-stage biotech with voclosporin (Lupkynis) approved for lupus nephritis; comparable business model targeting inflammatory kidney disease with a small specialty-pharma footprint.

TypeEmerging player
Description

Clinical-stage biotech developing cell therapy (REMDEL-001) for chronic kidney disease; overlaps with Arch's CKD Platform in targeting disease progression in advanced CKD patients.

TypeBroad incumbent
Description

Markets finerenone/Kerendia for CKD associated with type 2 diabetes; a large incumbent with adjacent kidney-disease franchise that could be a future acquirer or competitor to Arch's CKD program.

TypeBroad incumbent
Description

Major rare-disease player with established nephrology portfolio (e.g., ravulizumab in atypical HUS); a logical acquirer profile and broad benchmark for nephrology commercial economics.

TypeBroad incumbent
Description

Investing in kidney disease via its CMK-039 / APOL1 inhibitor program in collaboration with CRISPR Therapeutics; relevant as a well-capitalized incumbent expanding into nephrology and validating strategic interest in the space.

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 customers5 records

Each record includes

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

Segment3 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

Feature4 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

Subsidiaries1 record

Each record includes

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

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds9 records

Each record includes

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

Investors2 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&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 →

Arch Biopartners

Kidney Disease Therapeuticsarchbiopartners.com

Arch Biopartners is a Toronto-based, pre-revenue clinical-stage biotech developing DPEP-1 inhibiting therapeutics (LSALT peptide, cilastatin) for acute kidney injury and a recently acquired IL-32 platform for chronic kidney disease, conducting Phase II trials across nine global sites.

What Arch Biopartners does

Arch Biopartners is a clinical-stage biopharmaceutical company founded in 2010 and headquartered in Toronto, Canada, listed on the TSX Venture Exchange (ARCH) and OTCQB (ACHFF). The company develops novel therapeutics targeting acute kidney injury (AKI) and chronic kidney disease (CKD), anchored on the DPEP-1 (dipeptidase-1) inhibition pathway. Its scientific foundation draws on research from the University of Calgary's Snyder Institute, where Co-Founder and CSO Dr. Daniel Muruve leads the underlying biology. The company operates with a small team of 1-10 employees and has approximately 67.9 million common shares outstanding as of April 2026.

Arch's pipeline includes two Phase II-stage drug candidates: LSALT peptide (also referred to as Metablok), a proprietary DPEP-1 inhibitor being evaluated for cardiac surgery-associated acute kidney injury (CS-AKI), and cilastatin, a repurposed drug licensed from Telara Pharma (Spain) in April 2021 that is being evaluated in the 700-patient PONTiAK Phase II trial for toxin- and drug-induced AKI. In September 2025, the company expanded into chronic kidney disease through the acquisition of Lipdro Therapeutics Inc., adding a pre-clinical platform targeting IL-32. The platform is supported by composition-of-matter and method-of-use patents covering LSALT peptide, the licensed cilastatin rights, and the newly acquired IL-32 CKD IP.

The company is pre-revenue and funds operations through a combination of small non-brokered private placements, Canadian federal grants (notably CAD $4M from NRC IRAP in 2023 and CAD $750K from CIHR in 2021), and equity issuance. Clinical execution is currently distributed across nine trial sites globally, four in Canada and five international. The business model assumes future monetization through licensing, partnership, or direct commercialization of assets following Phase II/III readouts, rather than near-term product sales. Governance was strengthened in 2024-2025 by the appointment of Dr. Patrick Vink as Chairman, bringing senior commercial drug-development experience from Cubist Pharmaceuticals and Merck.

Arch Biopartners firmographics

Firmographics
Name
Arch Biopartners
Legal name
Arch Biopartners Inc.
Website
https://archbiopartners.com
Company type
Public
Founded year
2010
Operating status
Operating
Headcount range
1–10 employees
Short description
Arch Biopartners is a Toronto-based, pre-revenue clinical-stage biotech developing DPEP-1 inhibiting therapeutics (LSALT peptide, cilastatin) for acute kidney injury and a recently acquired IL-32 platform for chronic kidney disease, conducting Phase II trials across nine global sites.
Ownership category
akta.pro rank

Arch Biopartners industry classification

Industry
Product category
Kidney Disease Therapeutics
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical and Medicine Manufacturing (3254), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Rare Renal & Nephrology Disorder Therapies (HLAIAIAI)
akta.pro secondary industries
Nephrology & Urology Pharmaceuticals (HLAIAAAM), Nephrology & Urology Specialty Pharmaceuticals (HLAIACAH), Engineered Protein Therapeutics (de novo/AI-designed proteins, novel scaffolds) (HLAAAAAJ), Therapeutic Peptides & Protein/Peptide Biologics (HLAAAAAH)

Keywords

  • Acute kidney injury therapeutics
  • Chronic kidney disease treatments
  • DPEP-1 inhibitor drugs
  • Clinical stage biotech
  • Anti-inflammatory peptide drugs

Where Arch Biopartners is headquartered

Location

Headquarters

HQ city
Toronto
HQ country
Canada
HQ region
North America

Offices1 record

Markets served

Arch Biopartners business model

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

Revenue model

  1. Drug Development and Commercialization: Pre-revenue clinical stage biotech company. Revenue will be generated from commercialization of drug candidates LSALT peptide and cilastatin upon regulatory approval. Both drugs target acute kidney injury (AKI), a condition affecting over 10 million people annually in the U.S. and Europe, with an estimated worldwide market over $20 billion USD per year.
  2. Private Placements: The company raises capital through non-brokered private placement offerings of common shares to fund operations and clinical trials. Recent financings include $600,000 CAD (April 2026), $600,000 CAD (November 2025), and $500,000 CAD (November 2025).
  3. Government Grants and Funding: Non-dilutive funding from government agencies including NRC IRAP ($4 million in 2023) for clinical development activities and CIHR Team Grants ($750,000 in 2021) for pre-clinical and clinical trial design research.

Go-to-market motion1 record

Distribution channels3 records

Marketing channels8 records

Arch Biopartners product offering

Product offering

Core offering

Arch Biopartners is a clinical-stage therapeutic biotech company developing novel, on-target drug candidates for acute kidney injury (AKI) and chronic kidney disease (CKD). Its portfolio includes two lead DPEP-1 inhibitors in Phase II trials (LSALT peptide / Metablok for cardiac surgery-associated AKI and Cilastatin for toxin-induced AKI), plus a pre-clinical CKD platform targeting IL-32. The company acquires and develops these products and technology for sale to pharmaceutical companies.

Product overview

Arch Biopartners is a therapeutic biotech company developing a pipeline of novel, on-target drugs for kidney injury and disease. The company's portfolio spans both acute kidney injury (AKI) and chronic kidney disease (CKD) through three main programs: (1) LSALT Peptide (Metablok), a first-in-class DPEP1 inhibitor in Phase II trials for cardiac surgery-associated AKI; (2) Cilastatin, a repurposed DPEP1 inhibitor in Phase II trials targeting toxin-induced AKI; and (3) a pre-clinical CKD Platform targeting IL-32 for chronic kidney disease. The company also holds patents for both LSALT peptide and cilastatin as AKI treatments through the DPEP1 pathway.

Differentiator

Problem solved

Functional benefit

Brands

  • Metablok: Brand name for LSALT peptide drug candidate
  • PONTiAK

Products and services

  • LSALT Peptide (Metablok) A first-in-class DPEP-1 inhibitor peptide designed to protect the kidneys from ischemia-reperfusion injury during cardiac surgery. Currently in a global Phase II trial (CS-AKI) evaluating its ability to prevent acute kidney injury in patients undergoing on-pump cardiac surgery, with a recruitment target of 240 patients.
  • Cilastatin A repurposed DPEP-1 inhibitor being evaluated for its ability to block toxic drug uptake into the kidneys and prevent toxin-induced acute kidney injury caused by antibiotics, chemotherapeutics, and contrast agents. Currently in the Phase II PONTiAK trial (700 patients, CIHR/ACT funded).
  • CKD Platform (IL-32 Targeting) A pre-clinical research platform targeting IL-32, a non-classical cytokine directly implicated in diabetic kidney disease, the leading cause of kidney failure worldwide. The platform aims to develop novel, on-target therapeutics for chronic kidney disease based on research linking IL-32 to tubular injury in diabetic kidney disease.

Quantifiable outcome

  • 74% lower risk of AKI in randomized controlled trials (cilastatin)
  • +4 more outcomes

Companies that use Arch Biopartners

Customer profile

Named customers5 records

Segments3 records

Ideal customer profiles2 records

Arch Biopartners technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Arch Biopartners partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and major.

  • Fraser Health AuthoritycoreStrategic or Co-development Partner · 24 March 2026Clinical Trial Agreement enabling Royal Columbian Hospital to begin recruitment for Phase II trial evaluating LSALT peptide for cardiac surgery-associated AKI. Royal Columbian Hospital is the ninth site activated globally and fourth in Canada for the trial.
  • Lipdro Therapeutics Inc.majorStrategic or Co-development Partner · 5 November 2025Acquisition completed to strengthen company's position in kidney therapeutics and add breakthrough platform for developing new drugs targeting chronic kidney disease (CKD Platform).
  • Telara PharmacoreOEM/ Whitelabel/ Licensing Partner · 15 April 2021Worldwide exclusive license agreement for clinical development and marketing of cilastatin for treatment and prevention of acute kidney injury. Telara Pharma, a spin-off from Hospital General Gregorio Marañón in Madrid, Spain, provides Phase I safety data and established cilastatin drug manufacturing program. Patents unified with Arch's existing patent portfolio.
  • Hospital General Gregorio Marañón (Madrid, Spain)coreStrategic or Co-development Partner · 15 April 2021Public research hospital whose Nephrology Service (led by Drs. Alberto Tejedor and Alberto Lazaro) discovered the nephroprotective effect of cilastatin, resulting in patents for treatment of kidney damage caused by drugs and sepsis. Spin-off company Telara Pharma created to bring cilastatin to clinical use.
  • University of CalgarycoreStrategic or Co-development PartnerCore scientific research partner. Scientific team led by Dr. Daniel Muruve (CSO) and Dr. Justin Chun (Principal Scientist, CKD Platform) from the Cumming School of Medicine. Research established DPEP-1 pathway as therapeutic target for kidney inflammation.
  • Toronto General Hospital (UHN)coreStrategic or Co-development PartnerPhase II clinical trial site evaluating LSALT peptide for preventing AKI in on-pump cardiac surgery patients. Part of ongoing multi-center trial with recruitment target of 240 patients.
  • St. Michael's Hospital (Unity Health Toronto)coreStrategic or Co-development PartnerPhase II clinical trial site for LSALT peptide, third Canadian site to recruit patients. Ethics approval received December 2025; commenced patient dosing March 2026.

Scale indicators8 records

Recent moves7 records

Expansion highlights5 records

Arch Biopartners competitors and assessment

Company assessment

Direct peers

  • AM-Pharma: Clinical-stage biotech developing recombinant alkaline phosphatase for acute kidney injury; one of the most direct comparables to Arch's AKI-focused pipeline (acquired by Pfizer in 2022 in a deal valued at ~$1.3B).
  • Guard Therapeutics: Clinical-stage biotech developing RMC-035 (a small protein/peptide) for prevention of cardiac surgery-associated AKI; directly competes with Arch's LSALT peptide in the CS-AKI indication.

Emerging players

  • Angion Biomedica: Clinical-stage biotech focused on acute and chronic kidney injury with small-molecule and biologic candidates; comparable as a kidney-injury focused developer at similar development stage.
  • Travere Therapeutics: Late-stage clinical and commercial biotech with kidney disease programs (sparsentan/Filspari in IgA nephropathy and FSGS); overlaps with Arch on CKD therapeutics targeting rare kidney disorders.
  • Chinook Therapeutics: Clinical-stage nephrology biotech acquired by Novartis for up to ~$3.5B in 2023; pursued IgA nephropathy and other rare kidney diseases, validating big-pharma appetite for kidney assets at Arch's stage.
  • Aurinia Pharmaceuticals: Commercial-stage biotech with voclosporin (Lupkynis) approved for lupus nephritis; comparable business model targeting inflammatory kidney disease with a small specialty-pharma footprint.
  • ProKidney: Clinical-stage biotech developing cell therapy (REMDEL-001) for chronic kidney disease; overlaps with Arch's CKD Platform in targeting disease progression in advanced CKD patients.

Broad incumbents

  • Bayer (Nephrology Franchise): Markets finerenone/Kerendia for CKD associated with type 2 diabetes; a large incumbent with adjacent kidney-disease franchise that could be a future acquirer or competitor to Arch's CKD program.
  • AstraZeneca Rare Disease (Alexion): Major rare-disease player with established nephrology portfolio (e.g., ravulizumab in atypical HUS); a logical acquirer profile and broad benchmark for nephrology commercial economics.
  • Vertex Pharmaceuticals: Investing in kidney disease via its CMK-039 / APOL1 inhibitor program in collaboration with CRISPR Therapeutics; relevant as a well-capitalized incumbent expanding into nephrology and validating strategic interest in the space.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Arch Biopartners social profiles

Digital presence

Arch Biopartners financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Arch Biopartners leadership team

Management profile

Number of profiles

Profiles8 records

Arch Biopartners subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Arch Biopartners funding detail

Funding detail

Funding overview

Funding rounds9 records

Investors2 records

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

Arch Biopartners 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 Arch Biopartners

What does Arch Biopartners do?

Arch Biopartners is a clinical-stage therapeutic biotech company developing novel, on-target drug candidates for acute kidney injury (AKI) and chronic kidney disease (CKD). Its portfolio includes two lead DPEP-1 inhibitors in Phase II trials (LSALT peptide / Metablok for cardiac surgery-associated AKI and Cilastatin for toxin-induced AKI), plus a pre-clinical CKD platform targeting IL-32. The company acquires and develops these products and technology for sale to pharmaceutical companies.

Is Arch Biopartners a public or private company?

Arch Biopartners is a public company. It is classified as public and is currently operating.

When was Arch Biopartners founded?

Arch Biopartners was founded in 2010. It employs 1 to 10 people.

Where is Arch Biopartners based?

Arch Biopartners is headquartered in Toronto, Canada, in the North America region.

How does Arch Biopartners make money?

Three revenue lines are on record. Drug Development and Commercialization is the primary driver. The others are private Placements and government Grants and Funding.

Who are Arch Biopartners's main competitors?

Direct peers on record are AM-Pharma and Guard Therapeutics. Emerging players are Angion Biomedica, Travere Therapeutics, Chinook Therapeutics, Aurinia Pharmaceuticals and ProKidney. Broad incumbents are Bayer (Nephrology Franchise), AstraZeneca Rare Disease (Alexion) and Vertex Pharmaceuticals.

Does Arch Biopartners have an API?

No public API is recorded for Arch Biopartners.

What industry is Arch Biopartners in?

Arch Biopartners's product category is Kidney Disease Therapeutics. Its primary akta.pro industry code is HLAIAIAI, Rare Renal & Nephrology Disorder Therapies, with a secondary code of HLAIAAAM, Nephrology & Urology Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
MarketScreenerArch Biopartners Receives Review Board Approval Ahead of Phase 2 LSALT Trial ExpansionArch Biopartners received review board approval to expand its Phase 2 LSALT trial. The company is developing LSALT peptide and cilastatin for kidney injury, with a DPEP1 inhibitor in Phase II. The approval supports its integrated pipeline for acute and chronic kidney diseases.Financial PostArch Biopartners Receives Central IRB Approval to Support U.S. Sites in Phase II Cardiac Surgery-Associated Acute Kidney Injury Trial of LSALT PeptideArch Biopartners received central IRB approval to support U.S. sites in its Phase II trial of LSALT peptide for cardiac surgery-associated acute kidney injury. The trial is currently enrolling at Canadian sites, with a U.S. expansion underway. The company also has a cilastatin trial for toxin-induced AKI and a CKD platform.MarketScreenerArch Biopartners to Expand Ongoing Phase 2 LSAT Peptide Trial to The USArch Biopartners Inc. is expanding its ongoing Phase 2 clinical trial for the LSAT peptide to include sites in the United States. The LSAT peptide, a dipeptidase-1 inhibitor, is currently being developed to prevent cardiac surgery-associated acute kidney injury. This expansion marks a strategic progression in the company's pipeline for treating acute kidney conditions.YahooArch Biopartners to Expand Ongoing Phase 2 LSAT Peptide Trial to The USArch Biopartners will expand its Phase II trial of LSALT peptide into the United States. This trial will involve five institutions as part of the company's strategic growth plan. The expansion highlights Arch Biopartners' commitment to advancing its clinical research in the U.S.YahooArch Biopartners to Expand Phase II Cardiac Surgery-Associated Acute Kidney Injury Trial to the United StatesArch Biopartners Inc. is expanding its ongoing Phase II trial of the LSALT peptide targeting cardiac surgery-associated acute kidney injury into the United States, supported by interest from five leading U.S. clinical institutions. This expansion follows positive patient recruitment progress at existing sites in Canada and Turkey, with the aim of increasing access to eligible patients for the trial. The expected timeline for the new U.S. clinical sites to begin recruiting patients is four to six months, pending necessary approvals.BioSpaceArch Biopartners to Expand Phase II Cardiac Surgery-Associated Acute Kidney Injury Trial to the United StatesArch Biopartners announced it will expand its Phase II trial of LSALT peptide for cardiac surgery-associated acute kidney injury into the United States, following interest from five U.S. institutions. The trial has no adverse events and AKI has occurred consistently, supporting the expansion. U.S. sites are expected to require four to six months for preparation before dosing.AInvestArch Biopartners Hires U.S. Lab to Push IL-32 CKD Program-Why This 800M Patient Market Story Matters NowArch Biopartners has engaged a U.S.-based bioengineering laboratory to conduct pre-IND studies for its IL-32 program targeting chronic kidney disease, marking a transition from target validation to asset development. The company aims to generate proprietary data supporting method-of-use patent claims tied to IL-32's role in lipid droplet biology, inflammation, and tubular injury in diabetic kidney disease. With approximately 12-18 months of preclinical work ahead, including in vivo proof-of-concept and lead candidate optimization, success depends on data quality and financing, as Arch has raised CAD 600,000 for working capital.GlobeNewswireArch Biopartners Engages Private Laboratory to Accelerate IL-32 Chronic Kidney Disease ProgramArch Biopartners Inc. has engaged a U.S.-based laboratory specializing in bioengineering to accelerate its pre-IND IL-32 chronic kidney disease program targeting diabetic kidney disease. The laboratory will conduct studies to generate proprietary data and support the company's patent portfolio covering IL-32 drug candidates and related method-of-use claims, following peer-reviewed findings published in February 2026 that linked IL-32 to metabolic stress, chronic inflammation, and kidney injury in diabetic kidney disease. The company also provided an update on its ongoing month-to-month market-making agreement with Red Cloud Securities Inc., which is entitled to a monthly fee of C$5,000.BioSpaceArch Biopartners Engages Private Laboratory to Accelerate IL-32 Chronic Kidney Disease ProgramArch Biopartners engaged a U.S. laboratory to accelerate its pre-IND IL-32 chronic kidney disease program, generating proprietary data to support its patent portfolio. The company also entered a market-making agreement with Red Cloud Securities, effective April 2022, with a monthly cash fee of C$5,000.GlobeNewswireAcute Kidney Injury Clinical Trial Pipeline Appears Robust With 20+ Key Pharma Companies Actively Working in the Therapeutics Segment | DelveInsightDelveInsight's report on acute kidney injury (AKI) pipeline shows 20+ companies developing 25+ drugs, with about 12+ in late or mid-stage trials. Recent updates include Akebia's Phase I dosing of AKB-9090 and Arch Biopartners' Phase II trial recruitment for LSALT peptide. AstraZeneca's Phase III ARTEMIS data is expected in H2 2026.