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Modus Therapeutics

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uuid0000thh

Namestring
Modus Therapeutics
Legal namestring
Modus Therapeutics Holding AB (publ)
Websiteurl
modustx.com
Company typeenum
Public
Founded yearint
2018
Descriptiontext

Modus Therapeutics Holding AB (publ) is a Swedish clinical-stage biotechnology company developing sevuparin, a proprietary polysaccharide heparinoid drug candidate, for conditions characterized by severe systemic inflammation and iron dysregulation. The company was founded around 2018, listed on Nasdaq First North Growth Market (ticker MODTX) in July 2021, and is headquartered in Stockholm with 1-10 employees. Sevuparin's mechanism of action is multimodal: anti-inflammatory, anti-adhesive, and anti-aggregate effects, with markedly attenuated anticoagulant activity that enables several-fold higher dosing than standard heparinoids without bleeding risk. The compound has been administered to over 200 healthy volunteers and patients and can suppress hepcidin to 30-50% of baseline. Two formulations are in development: an IV formulation for in-patient administration and a subcutaneous formulation for ambulatory/home care.

The company's clinical pipeline has been repeatedly repositioned. A Phase 2 study in sickle cell disease completed in May 2019 did not show meaningful benefit in the total study population, prompting a strategic pivot in March 2021 under CEO John Öhd toward sepsis/septic shock as the lead indication. Subsequent programs have expanded into chronic kidney disease with anemia (Phase 2a enrolling 50-60 patients in Italy, first patient dosed December 2025) and severe malaria (in collaboration with Imperial College London and KEMRI-Wellcome Trust in Kenya, supported by Wellcome). Sevuparin has received FDA IND acceptance for sickle cell disease and FDA Rare Pediatric Disease Designation for pediatric SCD, and has been approved for clinical research in both the US and Europe.

Modus operates a partnership-focused business model and is pre-revenue. The stated strategy is to create product value through clinical milestones and ultimately license sevuparin to pharmaceutical partners with established market presence, with a target product approval/NDA around 2028/2029. Karolinska Development AB is the majority shareholder at 55.7% as of December 31, 2025, and has provided multiple bridge financings (SEK 7.0M in 2023, SEK 11.5M in 2022, SEK 5.0M in 2024, SEK 5.0M in 2025). A fully secured SEK 28.3 million rights issue in June 2025 extended cash runway through 2026.

Short descriptiontext

Modus Therapeutics is a Swedish clinical-stage biotech developing sevuparin, a proprietary non-anticoagulant heparinoid with anti-inflammatory properties, for sepsis, chronic kidney disease with anemia, severe malaria, and sickle cell disease, operating on a pre-revenue licensing/partnership business model.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersStockholm, Sweden
HQ citystring
Stockholm
HQ countrystring
Sweden
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage biotechnology, polysaccharide drug development, sepsis treatment research, sickle cell disease therapy, hepcidin suppression therapeutics
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
SIC code2 codes
  • Surgical & Medical Instruments & Apparatus3841
  • Biological Products, (No Disgnostic Substances)2836
Product category
Biopharmaceutical Drug Development
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Licensing/Royalty Revenue
TypeLicensing Royalties
Description

Pre-revenue biotech company. Business model is primarily based on partnership - attracting partnerships and buyers for sevuparin by creating product value through clinical research. Product value created through robust clinical data with value-building milestones to enable further value build with a partner that already has presence in the therapy area and its market. Target product approval/NDA around 2028/2029.

modustx.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 components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Modus Therapeutics is developing sevuparin, a proprietary polysaccharide (heparinoid) drug candidate with multimodal anti-inflammatory, anti-adhesive, and anti-aggregate effects. The company is conducting clinical development of sevuparin in IV and subcutaneous formulations as a potential treatment for sepsis/septic shock, severe malaria, anemia related to chronic kidney disease, and sickle cell disease. As a pre-revenue biotech, Modus plans to create product value through clinical milestones and commercialize via partnerships with established pharmaceutical companies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Plasma hepcidin reduced to 30-50% of baseline in healthy volunteers at clinically safe dose levels with peak effect between 6-24 hours
+2 more records
Product overview1 text field

Modus Therapeutics is a Swedish biotechnology company developing sevuparin, a proprietary polysaccharide drug candidate, as a potential treatment for several major healthcare conditions including sepsis/septic shock, severe malaria, and anemia related to chronic inflammation such as chronic kidney disease. The company operates as a single-product biotech with two formulation approaches: an IV formulation for in-patient hospital administration and a subcutaneous formulation for ambulatory and home care use. Sevuparin has a multimodal mechanism of action including anti-inflammatory, anti-adhesive, and anti-aggregate effects. The drug has been approved for clinical research in both the US and Europe and has been administered to over 200 healthy volunteers and patients in clinical trials.

Product and service1 record
1Sevuparin (IV formulation)
Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-06-11
Description

Clinical research collaboration with Professor Kathryn Maitland's team to evaluate sevuparin's effect in patients with severe malaria. The project is conducted in collaboration with KEMRI-Wellcome Trust Programme in Kilifi, Kenya. Imperial College is conducting the first clinical trial out of their specialized site in Kenya.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Longstanding collaboration with University of Brescia for evaluating sevuparin's potential in disorders with high levels of hepcidin such as anemia in chronic kidney disease and chronic inflammation disorders.

Strategic tierMinorTypeImplementation/ SI/ Consulting Partner
Description

Full-service contract clinical development organization with specialist expertise in orphan drug development. Co-development partner for the global Phase 2 study in sickle cell disease.

Strategic tierMinorTypeOthers
Description

Certified Adviser for Nasdaq First North Growth Market. Provides regulatory and market advice required for listing compliance.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Inotrem is a French clinical-stage biotech developing nangibotide (TREM-1 inhibitor) for septic shock. Both companies are developing novel therapeutics for sepsis/septic shock with similar partnership-driven business models and similar clinical stage.

TypeDirect peer
Description

AM-Pharma is a Dutch clinical-stage biotech developing recombinant human alkaline phosphatase for sepsis-associated acute kidney injury. Similar to Modus, AM-Pharma targets the sepsis inflammatory pathway and operates with a similar biotech business model.

TypeDirect peer
Description

Adrenomed is a German biotech developing adrecizumab, a monoclonal antibody targeting adrenomedullin for septic shock. Direct peer in the septic shock indication with similar clinical-stage development and biomarker-driven approach.

TypeDirect peer
Description

InflaRx is a German-US clinical-stage biotech developing vilobelimab, an anti-C5a monoclonal antibody for inflammatory conditions including sepsis. Comparable as a clinical-stage inflammation biotech targeting complement/inflammatory pathways.

TypeDirect peer
Description

Agios Pharmaceuticals develops mitapivat for sickle cell disease and other hemolytic anemias. Directly comparable in SCD therapeutic development with overlapping mechanism on red blood cell function and similar indication overlap to sevuparin.

TypeDirect peer
Description

GBT developed Oxbryta (voxelotor) for sickle cell disease and was acquired by Pfizer for $5.4B in 2022. Direct competitor in the SCD therapeutic market with an approved product addressing similar vaso-occlusive mechanisms.

TypeDirect peer
Description

Emmaus Life Sciences commercializes Endari (L-glutamine), an FDA-approved treatment for sickle cell disease. Directly comparable as an SCD-focused company targeting vaso-occlusive complications and acute complications.

TypeDirect peer
Description

Akebia Therapeutics developed vadadustat, an oral HIF-PH inhibitor for anemia of chronic kidney disease. Direct competitor in the CKD-anemia therapeutic space with similar patient population focus and mechanism targeting erythropoiesis.

TypeDirect peer
Description

FibroGen developed roxadustat, an HIF-PH inhibitor approved in multiple geographies for CKD-anemia. Comparable peer with similar therapeutic focus on anemia in CKD patients, addressing the hepcidin-mediated iron restriction pathway.

TypeBroad incumbent
Description

Vertex Pharmaceuticals co-developed Casgevy (exa-cel) with CRISPR Therapeutics, the first FDA-approved CRISPR gene therapy for sickle cell disease. Broader incumbent competing in SCD space with a curative gene therapy approach versus Modus's symptomatic sevuparin approach.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 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

Segment4 records

Each record includes

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

Ideal customer profile1 record

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
Profiles5 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 rounds7 records

Each record includes

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

Investors6 records

Each record includes

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

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

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

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

Modus Therapeutics

Biopharmaceutical Drug Developmentmodustx.com

Modus Therapeutics is a Swedish clinical-stage biotech developing sevuparin, a proprietary non-anticoagulant heparinoid with anti-inflammatory properties, for sepsis, chronic kidney disease with anemia, severe malaria, and sickle cell disease, operating on a pre-revenue licensing/partnership business model.

What Modus Therapeutics does

Modus Therapeutics Holding AB (publ) is a Swedish clinical-stage biotechnology company developing sevuparin, a proprietary polysaccharide heparinoid drug candidate, for conditions characterized by severe systemic inflammation and iron dysregulation. The company was founded around 2018, listed on Nasdaq First North Growth Market (ticker MODTX) in July 2021, and is headquartered in Stockholm with 1-10 employees. Sevuparin's mechanism of action is multimodal: anti-inflammatory, anti-adhesive, and anti-aggregate effects, with markedly attenuated anticoagulant activity that enables several-fold higher dosing than standard heparinoids without bleeding risk. The compound has been administered to over 200 healthy volunteers and patients and can suppress hepcidin to 30-50% of baseline. Two formulations are in development: an IV formulation for in-patient administration and a subcutaneous formulation for ambulatory/home care.

The company's clinical pipeline has been repeatedly repositioned. A Phase 2 study in sickle cell disease completed in May 2019 did not show meaningful benefit in the total study population, prompting a strategic pivot in March 2021 under CEO John Öhd toward sepsis/septic shock as the lead indication. Subsequent programs have expanded into chronic kidney disease with anemia (Phase 2a enrolling 50-60 patients in Italy, first patient dosed December 2025) and severe malaria (in collaboration with Imperial College London and KEMRI-Wellcome Trust in Kenya, supported by Wellcome). Sevuparin has received FDA IND acceptance for sickle cell disease and FDA Rare Pediatric Disease Designation for pediatric SCD, and has been approved for clinical research in both the US and Europe.

Modus operates a partnership-focused business model and is pre-revenue. The stated strategy is to create product value through clinical milestones and ultimately license sevuparin to pharmaceutical partners with established market presence, with a target product approval/NDA around 2028/2029. Karolinska Development AB is the majority shareholder at 55.7% as of December 31, 2025, and has provided multiple bridge financings (SEK 7.0M in 2023, SEK 11.5M in 2022, SEK 5.0M in 2024, SEK 5.0M in 2025). A fully secured SEK 28.3 million rights issue in June 2025 extended cash runway through 2026.

Modus Therapeutics firmographics

Firmographics
Name
Modus Therapeutics
Legal name
Modus Therapeutics Holding AB (publ)
Website
https://modustx.com
Company type
Public
Founded year
2018
Operating status
Operating
Headcount range
1–10 employees
Short description
Modus Therapeutics is a Swedish clinical-stage biotech developing sevuparin, a proprietary non-anticoagulant heparinoid with anti-inflammatory properties, for sepsis, chronic kidney disease with anemia, severe malaria, and sickle cell disease, operating on a pre-revenue licensing/partnership business model.
Ownership category
akta.pro rank

Where Modus Therapeutics is headquartered

Location

Headquarters

HQ city
Stockholm
HQ country
Sweden
HQ region
Europe

Offices1 record

Markets served

Modus Therapeutics business model

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

Revenue model

  1. Pharmaceutical Licensing/Royalty Revenue: Pre-revenue biotech company. Business model is primarily based on partnership - attracting partnerships and buyers for sevuparin by creating product value through clinical research. Product value created through robust clinical data with value-building milestones to enable further value build with a partner that already has presence in the therapy area and its market. Target product approval/NDA around 2028/2029.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Modus Therapeutics product offering

Product offering

Core offering

Modus Therapeutics is developing sevuparin, a proprietary polysaccharide (heparinoid) drug candidate with multimodal anti-inflammatory, anti-adhesive, and anti-aggregate effects. The company is conducting clinical development of sevuparin in IV and subcutaneous formulations as a potential treatment for sepsis/septic shock, severe malaria, anemia related to chronic kidney disease, and sickle cell disease. As a pre-revenue biotech, Modus plans to create product value through clinical milestones and commercialize via partnerships with established pharmaceutical companies.

Product overview

Modus Therapeutics is a Swedish biotechnology company developing sevuparin, a proprietary polysaccharide drug candidate, as a potential treatment for several major healthcare conditions including sepsis/septic shock, severe malaria, and anemia related to chronic inflammation such as chronic kidney disease. The company operates as a single-product biotech with two formulation approaches: an IV formulation for in-patient hospital administration and a subcutaneous formulation for ambulatory and home care use. Sevuparin has a multimodal mechanism of action including anti-inflammatory, anti-adhesive, and anti-aggregate effects. The drug has been approved for clinical research in both the US and Europe and has been administered to over 200 healthy volunteers and patients in clinical trials.

Differentiator

Problem solved

Functional benefit

Products and services

  • Sevuparin (IV formulation)

Quantifiable outcome

  • Plasma hepcidin reduced to 30-50% of baseline in healthy volunteers at clinically safe dose levels with peak effect between 6-24 hours
  • +2 more outcomes

Companies that use Modus Therapeutics

Customer profile

Segments4 records

Ideal customer profiles1 record

Modus Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Modus Therapeutics partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Imperial College LondoncoreStrategic or Co-development Partner · 11 June 2021Clinical research collaboration with Professor Kathryn Maitland's team to evaluate sevuparin's effect in patients with severe malaria. The project is conducted in collaboration with KEMRI-Wellcome Trust Programme in Kilifi, Kenya. Imperial College is conducting the first clinical trial out of their specialized site in Kenya.
  • University of BresciacoreStrategic or Co-development PartnerLongstanding collaboration with University of Brescia for evaluating sevuparin's potential in disorders with high levels of hepcidin such as anemia in chronic kidney disease and chronic inflammation disorders.
  • ErgomedminorImplementation/ SI/ Consulting PartnerFull-service contract clinical development organization with specialist expertise in orphan drug development. Co-development partner for the global Phase 2 study in sickle cell disease.
  • Bergs Securities ABminorOthersCertified Adviser for Nasdaq First North Growth Market. Provides regulatory and market advice required for listing compliance.

Scale indicators11 records

Recent moves7 records

Expansion highlights5 records

Modus Therapeutics competitors and assessment

Company assessment

Direct peers

  • Inotrem: Inotrem is a French clinical-stage biotech developing nangibotide (TREM-1 inhibitor) for septic shock. Both companies are developing novel therapeutics for sepsis/septic shock with similar partnership-driven business models and similar clinical stage.
  • AM-Pharma: AM-Pharma is a Dutch clinical-stage biotech developing recombinant human alkaline phosphatase for sepsis-associated acute kidney injury. Similar to Modus, AM-Pharma targets the sepsis inflammatory pathway and operates with a similar biotech business model.
  • Adrenomed: Adrenomed is a German biotech developing adrecizumab, a monoclonal antibody targeting adrenomedullin for septic shock. Direct peer in the septic shock indication with similar clinical-stage development and biomarker-driven approach.
  • InflaRx: InflaRx is a German-US clinical-stage biotech developing vilobelimab, an anti-C5a monoclonal antibody for inflammatory conditions including sepsis. Comparable as a clinical-stage inflammation biotech targeting complement/inflammatory pathways.
  • Agios Pharmaceuticals: Agios Pharmaceuticals develops mitapivat for sickle cell disease and other hemolytic anemias. Directly comparable in SCD therapeutic development with overlapping mechanism on red blood cell function and similar indication overlap to sevuparin.
  • Global Blood Therapeutics (Pfizer): GBT developed Oxbryta (voxelotor) for sickle cell disease and was acquired by Pfizer for $5.4B in 2022. Direct competitor in the SCD therapeutic market with an approved product addressing similar vaso-occlusive mechanisms.
  • Emmaus Life Sciences: Emmaus Life Sciences commercializes Endari (L-glutamine), an FDA-approved treatment for sickle cell disease. Directly comparable as an SCD-focused company targeting vaso-occlusive complications and acute complications.
  • Akebia Therapeutics: Akebia Therapeutics developed vadadustat, an oral HIF-PH inhibitor for anemia of chronic kidney disease. Direct competitor in the CKD-anemia therapeutic space with similar patient population focus and mechanism targeting erythropoiesis.
  • FibroGen: FibroGen developed roxadustat, an HIF-PH inhibitor approved in multiple geographies for CKD-anemia. Comparable peer with similar therapeutic focus on anemia in CKD patients, addressing the hepcidin-mediated iron restriction pathway.

Broad incumbents

  • Vertex Pharmaceuticals: Vertex Pharmaceuticals co-developed Casgevy (exa-cel) with CRISPR Therapeutics, the first FDA-approved CRISPR gene therapy for sickle cell disease. Broader incumbent competing in SCD space with a curative gene therapy approach versus Modus's symptomatic sevuparin approach.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Modus Therapeutics social profiles

Digital presence

Modus Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Modus Therapeutics leadership team

Management profile

Number of profiles

Profiles5 records

Modus Therapeutics funding detail

Funding detail

Funding overview

Funding rounds7 records

Investors6 records

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

Modus Therapeutics 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 Modus Therapeutics

What does Modus Therapeutics do?

Modus Therapeutics is developing sevuparin, a proprietary polysaccharide (heparinoid) drug candidate with multimodal anti-inflammatory, anti-adhesive, and anti-aggregate effects. The company is conducting clinical development of sevuparin in IV and subcutaneous formulations as a potential treatment for sepsis/septic shock, severe malaria, anemia related to chronic kidney disease, and sickle cell disease. As a pre-revenue biotech, Modus plans to create product value through clinical milestones and commercialize via partnerships with established pharmaceutical companies.

Is Modus Therapeutics a public or private company?

Modus Therapeutics is a public company. It is classified as public and is currently operating.

When was Modus Therapeutics founded?

Modus Therapeutics was founded in 2018. It employs 1 to 10 people.

Where is Modus Therapeutics based?

Modus Therapeutics is headquartered in Stockholm, Sweden, in the Europe region.

How does Modus Therapeutics make money?

One revenue line is on record: pharmaceutical Licensing/Royalty Revenue.

Who are Modus Therapeutics's main competitors?

Direct peers on record are Inotrem, AM-Pharma, Adrenomed, InflaRx, Agios Pharmaceuticals, Global Blood Therapeutics (Pfizer), Emmaus Life Sciences, Akebia Therapeutics and FibroGen. Vertex Pharmaceuticals is listed as a broad incumbent.

Does Modus Therapeutics have an API?

No public API is recorded for Modus Therapeutics.

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Live signals
TradingViewKDventures portfolio company Modus Therapeutics temporarily pauses enrollment in Phase 2a study of sevuparin in chronic kidney disease with anemiaModus Therapeutics temporarily paused enrollment in its Phase 2a study of sevuparin for chronic kidney disease with anemia after a serious adverse event was reported as a SUSAR. The pause is precautionary, not regulatory, and may shift the proof-of-concept readout to the first quarter of 2027. The company is evaluating data to determine next steps.The future of tradingModus Therapeutics pauses enrollment in Phase IIa sevuparin trial after serious adverse eventModus Therapeutics paused enrollment in Part 2 of its Phase IIa sevuparin trial for chronic kidney disease with anemia after a serious adverse event, with no causal link established. The pause was not regulator-imposed, and proof-of-concept results are now expected in the first quarter of 2027, versus around the turn of 2026/2027 previously.TradingViewModus Therapeutics Holding AB (publ) (MODTX) Pauses Phase IIa Enrollment After SUSARModus Therapeutics paused enrollment in Part 2 of its Phase IIa sevuparin CKD anemia study after a reported SUSAR. The voluntary pause shifts the proof-of-concept readout to Q1 2027, with cash expected to fund operations into Q2 2027.YahooKarolinska Development's portfolio company Modus Therapeutics initiates dosing in phase 2a study in patients with chronic kidney disease with anemiaKarolinska Development's portfolio company Modus Therapeutics has dosed the first patient in the phase 2a clinical study of sevuparin for treating chronic kidney disease with anemia. The study, conducted in Italy with 50-60 patients, will evaluate repeated dosing safety and clinically relevant efficacy outcomes including effects on hemoglobin and hepcidin levels. This milestone follows regulatory approval and aligns with the company's previously communicated development schedule, marking continued progress in the clinical program.PharmiWeb.comFirst Patient Dosed in Part 2 of Modus Therapeutics’ Phase IIa Study in Chronic Kidney Disease with AnemiaModus Therapeutics Holding AB announced on December 10, 2025, that the first patient has been dosed in Part 2 of its ongoing Phase IIa clinical study evaluating sevuparin for the treatment of Chronic Kidney Disease with anemia. Part 2 represents the proof-of-concept phase following completion of Part 1 in Q2 2025, with the study focusing on repeated-dose safety and efficacy outcomes including hemoglobin and hepcidin levels across 50-60 patients. The trial is being conducted at two nephrology centers in Italy in collaboration with CRO Latis S.r.l.GlobeNewswireKarolinska Development's portfolio company Modus Therapeutics initiates dosing in phase 2a study in patients with chronic kidney disease with anemiaKarolinska Development announced that its portfolio company Modus Therapeutics has initiated dosing in the second part of a phase 2a clinical study evaluating sevuparin as a treatment for chronic kidney disease with anemia in Italy. The study will enroll 50–60 patients and evaluate repeated dosing safety and efficacy, including effects on hemoglobin and hepcidin biomarkers, building on positive results from the first part completed in July which showed sevuparin was well tolerated. Karolinska Development holds 54% direct and 1% indirect ownership in Modus Therapeutics, which is listed on Nasdaq First North Growth Market.PharmaTimesModus Therapeutics advances sevuparin study in chronic kidney disease with anemiaModus Therapeutics Holding AB has dosed the first patient in Part 2 of its ongoing Phase 2a clinical study evaluating sevuparin for the treatment of chronic kidney disease with anemia, following completion of Part 1 earlier in 2025. Part 2 focuses on repeated-dose evaluation, examining safety and outcomes including hemoglobin and hepcidin levels in patients with advanced CKD and anemia, with the study expected to enroll 50–60 patients across both parts. Sevuparin is an investigational heparinoid designed to address unmet medical needs in CKD with anemia and potentially other chronic inflammatory conditions.GlobeNewswireInterim Report - January-September 2025Karolinska Development AB published its Q3 2025 interim report, reporting a net loss of SEK 66.8 million for the quarter and a net loss of SEK 154.3 million for the period. The portfolio's fair value fell to SEK 1,346.7 million, down SEK 38.2 million from the previous quarter, mainly due to Umecrine Cognition and Modus Therapeutics.GlobeNewswireInterim Report - January-September 2025Karolinska Development AB published its interim report for January-September 2025 on November 14, 2025, reporting a net loss of SEK -66.8 million for Q3 2025, significantly wider than the SEK -10.9 million loss in Q3 2024, driven primarily by a change in fair value of portfolio companies of SEK -65.4 million due to adjustments in Umecrine Cognition's market value and a decline in Modus Therapeutics' share price. The portfolio fair value decreased to SEK 1,346.7 million at end of September 2025 from SEK 1,384.9 million at end of June 2025. Multiple portfolio companies reported clinical and funding milestones during the period, including Modus Therapeutics completing patient enrollment for its sevuparin Phase 2a study and BOOST Pharma raising SEK 34 million and presenting positive two-year follow-up data from its BT-101 cell therapy trial.GlobeNewswireKarolinska Development's portfolio company Modus Therapeutics receives approval for second part of phase 2 study in chronic kidney disease with anemiaModus Therapeutics received regulatory approval to initiate the second part of its phase 2 study with sevuparin for chronic kidney disease with anemia, to be started in Q4 2025. The study will evaluate three doses of sevuparin based on single-dose data from the initial part, which showed good tolerability.