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Keros Therapeutics

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uuid00026pz

Namestring
Keros Therapeutics
Legal namestring
Keros Therapeutics, Inc.
Websiteurl
kerostx.com
Company typeenum
Public
Founded yearint
2015
Descriptiontext

Keros Therapeutics is a clinical-stage biopharmaceutical company founded in 2015 and headquartered in Lexington, Massachusetts, that develops novel therapeutics modulating the transforming growth factor-beta (TGF-β) superfamily signaling pathway. The company's pipeline centers on two investigational candidates: elritercept (KER-050), an activin receptor type IIA fusion protein targeting ineffective hematopoiesis in myelodysplastic syndromes (MDS) and myelofibrosis; and rinvatercept (KER-065), a selective activin receptor ligand trap designed to address neuromuscular disorders including Duchenne muscular dystrophy (DMD) and amyotrophic lateral sclerosis (ALS). Both candidates are designed to address multiple pathophysiologies simultaneously — affecting muscle, bone, fat, fibrosis, and blood cell lineages — based on deep expertise in the TGF-β superfamily, which encompasses more than 30 ligands and 12 receptors.

Keros operates a traditional pharma commercialization model, advancing candidates through clinical trials and seeking regulatory approvals, with global commercialization of elritercept (excluding mainland China, Hong Kong, and Macau) licensed to Takeda Pharmaceuticals under an agreement signed in December 2024 and effective January 2025. The company generates nominal revenue from this license (Q1 2026 revenue of approximately $0.39M) while incurring ongoing R&D expenses, and funds operations through equity financing — including a $140M public offering in January 2024 — supplemented by a $375M capital return program announced in October 2025 that returned cash to shareholders. The company has 101-250 employees and is led by founder/CEO Jasbir Seehra, with a board chaired by former BioMarin CEO Jean-Jacques Bienaimé.

The company's target patient populations include 60,000-170,000 MDS patients in the US, 16,000-18,500 myelofibrosis patients in the US, and approximately 1 in 3,500 male births worldwide affected by DMD, representing rare disease markets with significant unmet medical need and potential for orphan drug exclusivity. Distribution is currently restricted to clinical trial sites for ongoing Phase 2 and Phase 3 studies, with future commercial distribution expected through traditional pharmaceutical channels via the Takeda partnership for elritercept.

Short descriptiontext

Keros Therapeutics is a clinical-stage biopharmaceutical company developing TGF-β-modulating therapeutics for hematological disorders (MDS, myelofibrosis) and neuromuscular diseases (DMD, ALS), with elritercept licensed to Takeda for global commercialization.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersLexington, United States
HQ citystring
Lexington
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage biopharmaceuticals, TGF-beta therapeutics, hematology drug development, neuromuscular disorder treatments, activin receptor fusion proteins
Industry1 code
1Genetic & Genomic Rare Disease Therapeutics
CodeHLAIAIAAPrimaryYes
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Clinical-stage biopharmaceuticals
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1License Agreement Revenue
TypeLicensing Royalties
Description

Keros receives revenue from its exclusive license agreement with Takeda Pharmaceuticals U.S.A., Inc. for elritercept. The agreement was signed in December 2024 and became effective January 2025, granting Takeda rights to develop, manufacture and commercialize elritercept worldwide outside mainland China, Hong Kong and Macau. Keros may receive milestone payments and royalties on net sales.

globenewswire.com
2Pharmaceutical Product Sales
TypeOne Time License
Description

Pre-revenue clinical-stage company. Future revenue will come from commercialization of approved therapeutics following successful clinical development and regulatory approval.

defenseworld.net
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

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

Keros Therapeutics is a clinical-stage biopharmaceutical company that discovers, develops, and commercializes novel therapeutics targeting the transforming growth factor-beta (TGF-β) superfamily signaling pathway. Its lead product candidates are elritercept (KER-050), an ActRIIA fusion protein for hematological disorders such as myelodysplastic syndromes (MDS) and myelofibrosis, and rinvatercept (KER-065), a selective activin receptor ligand trap for neuromuscular disorders including Duchenne muscular dystrophy (DMD) and amyotrophic lateral sclerosis (ALS). Elritercept has been licensed to Takeda for global commercialization outside mainland China, Hong Kong, and Macau.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Phase 1 trial of KER-065 showed it was generally well-tolerated with no serious adverse events or dose-limiting toxicities reported
+2 more records
Product and service2 records
1Elritercept (KER-050)
CategoryBiopharmaceutical therapeutics
Description

Investigational activin receptor type IIA (ActRIIA) fusion protein designed to inhibit select TGF-β ligands including activin A. Being developed for treatment of ineffective hematopoiesis in myelodysplastic syndromes (MDS) and myelofibrosis (MF). Has potential to increase red blood cell and platelet production while improving bone health. Licensed to Takeda for global commercialization outside mainland China, Hong Kong and Macau.

2Rinvatercept (KER-065)
CategoryBiopharmaceutical therapeutics
Description

Investigational selective activin receptor ligand trap designed to inhibit biological effects of myostatin and activin A. Targets neuromuscular disorders including Duchenne muscular dystrophy (DMD) and ALS. Designed to increase skeletal muscle regeneration, muscle size and strength, reduce body fat, reduce skeletal muscle fibrosis, and increase bone strength.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
1Sean M. Healey & AMG Center for ALS (Massachusetts General Hospital)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-09
Description

Collaboration for design of Phase 2 clinical trial evaluating rinvatercept in patients with amyotrophic lateral sclerosis (ALS) within the Healey ALS MyMatch program. This biomarker-driven personalized trial initiative matches ALS patient subgroups to experimental therapies based on genetic and biofluid markers.

biospace.com
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2024-12-01
Description

Exclusive license agreement for elritercept (KER-050) granted to Takeda to further develop, manufacture and commercialize worldwide outside mainland China, Hong Kong and Macau. Agreement became effective January 2025. This partnership leverages Takeda's global commercial infrastructure for hematology products.

Strategic tierMinorTypeOthers
Description

Patient advocacy organization for MDS patients, listed as a patient resource on Keros website.

4The MDS Foundation
Strategic tierMinorTypeOthers
Description

Patient advocacy organization supporting MDS patients, listed as a patient resource on Keros website.

kerostx.com
Strategic tierMinorTypeOthers
Description

Patient advocacy organization for myeloproliferative neoplasms including myelofibrosis, listed as a patient resource on Keros website.

Strategic tierMinorTypeOthers
Description

Patient advocacy organization for Duchenne muscular dystrophy, listed as a patient resource on Keros website.

Strategic tierMinorTypeOthers
Description

International patient advocacy network for neuromuscular diseases, listed as a patient resource on Keros website.

Recent move10 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Founded by Keros CEO Jasbir Seehra, Acceleron pioneered the activin receptor ligand-trap approach (luspatercept/Reblozyl, sotatercept) and was acquired by Merck for ~$11.5B. Closest platform analog and direct precedent for the value of Keros' TGF-β assets.

TypeBroad incumbent
Description

Markets Reblozyl (luspatercept), an activin receptor Fc fusion approved in lower-risk MDS — the most direct competitive and mechanistic overlap with elritercept. BMS sets the benchmark Keros must beat in MDS.

TypeDirect peer
Description

Clinical-stage biotech developing apitegromab, a myostatin-activating antibody for SMA — directly targets the same TGF-β / myostatin axis Keros is pursuing with KER-065 in DMD and ALS.

TypeDirect peer
Description

Established DMD franchise (Elevidys gene therapy, EXONDYS 51, VYONDYS 53). Defines the competitive standard and pricing precedent for any DMD therapy including KER-065.

TypeDirect peer
Description

Developed and commercialized the first DMD therapy (drisapersen program) and operates a rare-hematology/rare-disease commercial platform. Keros Chairman Jean-Jacques Bienaime is BioMarin's former CEO/Chair.

TypeEmerging player
Description

Late-stage biotech with imetelstat approved in lower-risk MDS — competing for the same prescriber base as elritercept in MDS, making it a relevant adjacent competitor in Keros' core indication.

TypeEmerging player
Description

Clinical-stage rare-disease biotech (roxadustat, pamrevlumab) with comparable size, clinical-stage profile and rare-disease focus. Useful comparator for Keros' market cap and burn dynamics.

TypeEmerging player
Description

Clinical-stage hematology biotech focused on rare anemias and disorders of ineffective erythropoiesis — overlapping therapeutic area with Keros' elritercept MDS/MF program.

TypeEmerging player
Description

Antisense oligonucleotide platform with neuromuscular programs (e.g., tofersen in SOD1-ALS). Direct overlap with Keros' ALS strategy via the Healey MyMatch program.

TypeEmerging player
Description

Rare hematology biotech with pipeline assets targeting complement-mediated and bleeding disorders. Comparable clinical-stage rare-hematology profile to Keros' elritercept franchise.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 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 highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

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

Segment4 records

Each record includes

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

Ideal customer profile3 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
Profiles12 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 rounds5 records

Each record includes

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

Investors10 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 →

Keros Therapeutics

Clinical-stage biopharmaceuticalskerostx.com

Keros Therapeutics is a clinical-stage biopharmaceutical company developing TGF-β-modulating therapeutics for hematological disorders (MDS, myelofibrosis) and neuromuscular diseases (DMD, ALS), with elritercept licensed to Takeda for global commercialization.

What Keros Therapeutics does

Keros Therapeutics is a clinical-stage biopharmaceutical company founded in 2015 and headquartered in Lexington, Massachusetts, that develops novel therapeutics modulating the transforming growth factor-beta (TGF-β) superfamily signaling pathway. The company's pipeline centers on two investigational candidates: elritercept (KER-050), an activin receptor type IIA fusion protein targeting ineffective hematopoiesis in myelodysplastic syndromes (MDS) and myelofibrosis; and rinvatercept (KER-065), a selective activin receptor ligand trap designed to address neuromuscular disorders including Duchenne muscular dystrophy (DMD) and amyotrophic lateral sclerosis (ALS). Both candidates are designed to address multiple pathophysiologies simultaneously — affecting muscle, bone, fat, fibrosis, and blood cell lineages — based on deep expertise in the TGF-β superfamily, which encompasses more than 30 ligands and 12 receptors.

Keros operates a traditional pharma commercialization model, advancing candidates through clinical trials and seeking regulatory approvals, with global commercialization of elritercept (excluding mainland China, Hong Kong, and Macau) licensed to Takeda Pharmaceuticals under an agreement signed in December 2024 and effective January 2025. The company generates nominal revenue from this license (Q1 2026 revenue of approximately $0.39M) while incurring ongoing R&D expenses, and funds operations through equity financing — including a $140M public offering in January 2024 — supplemented by a $375M capital return program announced in October 2025 that returned cash to shareholders. The company has 101-250 employees and is led by founder/CEO Jasbir Seehra, with a board chaired by former BioMarin CEO Jean-Jacques Bienaimé.

The company's target patient populations include 60,000-170,000 MDS patients in the US, 16,000-18,500 myelofibrosis patients in the US, and approximately 1 in 3,500 male births worldwide affected by DMD, representing rare disease markets with significant unmet medical need and potential for orphan drug exclusivity. Distribution is currently restricted to clinical trial sites for ongoing Phase 2 and Phase 3 studies, with future commercial distribution expected through traditional pharmaceutical channels via the Takeda partnership for elritercept.

Keros Therapeutics firmographics

Firmographics
Name
Keros Therapeutics
Legal name
Keros Therapeutics, Inc.
Website
https://kerostx.com
Company type
Public
Founded year
2015
Operating status
Operating
Headcount range
101–250 employees
Short description
Keros Therapeutics is a clinical-stage biopharmaceutical company developing TGF-β-modulating therapeutics for hematological disorders (MDS, myelofibrosis) and neuromuscular diseases (DMD, ALS), with elritercept licensed to Takeda for global commercialization.
Ownership category
akta.pro rank

Keros Therapeutics industry classification

Industry
Product category
Clinical-stage biopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Genetic & Genomic Rare Disease Therapeutics (HLAIAIAA)

Keywords

  • Clinical-stage biopharmaceuticals
  • TGF-beta therapeutics
  • Hematology drug development
  • Neuromuscular disorder treatments
  • Activin receptor fusion proteins

Where Keros Therapeutics is headquartered

Location

Headquarters

HQ city
Lexington
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Keros 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. License Agreement Revenue: Keros receives revenue from its exclusive license agreement with Takeda Pharmaceuticals U.S.A., Inc. for elritercept. The agreement was signed in December 2024 and became effective January 2025, granting Takeda rights to develop, manufacture and commercialize elritercept worldwide outside mainland China, Hong Kong and Macau. Keros may receive milestone payments and royalties on net sales.
  2. Pharmaceutical Product Sales: Pre-revenue clinical-stage company. Future revenue will come from commercialization of approved therapeutics following successful clinical development and regulatory approval.

Go-to-market motion2 records

Distribution channels2 records

Marketing channels4 records

Keros Therapeutics product offering

Product offering

Core offering

Keros Therapeutics is a clinical-stage biopharmaceutical company that discovers, develops, and commercializes novel therapeutics targeting the transforming growth factor-beta (TGF-β) superfamily signaling pathway. Its lead product candidates are elritercept (KER-050), an ActRIIA fusion protein for hematological disorders such as myelodysplastic syndromes (MDS) and myelofibrosis, and rinvatercept (KER-065), a selective activin receptor ligand trap for neuromuscular disorders including Duchenne muscular dystrophy (DMD) and amyotrophic lateral sclerosis (ALS). Elritercept has been licensed to Takeda for global commercialization outside mainland China, Hong Kong, and Macau.

Differentiator

Problem solved

Functional benefit

Products and services

  • Elritercept (KER-050) Investigational activin receptor type IIA (ActRIIA) fusion protein designed to inhibit select TGF-β ligands including activin A. Being developed for treatment of ineffective hematopoiesis in myelodysplastic syndromes (MDS) and myelofibrosis (MF). Has potential to increase red blood cell and platelet production while improving bone health. Licensed to Takeda for global commercialization outside mainland China, Hong Kong and Macau.
  • Rinvatercept (KER-065) Investigational selective activin receptor ligand trap designed to inhibit biological effects of myostatin and activin A. Targets neuromuscular disorders including Duchenne muscular dystrophy (DMD) and ALS. Designed to increase skeletal muscle regeneration, muscle size and strength, reduce body fat, reduce skeletal muscle fibrosis, and increase bone strength.

Quantifiable outcome

  • Phase 1 trial of KER-065 showed it was generally well-tolerated with no serious adverse events or dose-limiting toxicities reported
  • +2 more outcomes

Companies that use Keros Therapeutics

Customer profile

Named customers4 records

Segments4 records

Ideal customer profiles3 records

Keros Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Keros Therapeutics partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and minor.

  • Sean M. Healey & AMG Center for ALS (Massachusetts General Hospital)coreStrategic or Co-development Partner · 9 March 2026Collaboration for design of Phase 2 clinical trial evaluating rinvatercept in patients with amyotrophic lateral sclerosis (ALS) within the Healey ALS MyMatch program. This biomarker-driven personalized trial initiative matches ALS patient subgroups to experimental therapies based on genetic and biofluid markers.
  • Takeda Pharmaceuticals U.S.A., Inc.coreOEM/ Whitelabel/ Licensing Partner · 1 December 2024Exclusive license agreement for elritercept (KER-050) granted to Takeda to further develop, manufacture and commercialize worldwide outside mainland China, Hong Kong and Macau. Agreement became effective January 2025. This partnership leverages Takeda's global commercial infrastructure for hematology products.
  • Aplastic Anemia & MDS International FoundationminorOthersPatient advocacy organization for MDS patients, listed as a patient resource on Keros website.
  • The MDS FoundationminorOthersPatient advocacy organization supporting MDS patients, listed as a patient resource on Keros website.
  • MPN Research FoundationminorOthersPatient advocacy organization for myeloproliferative neoplasms including myelofibrosis, listed as a patient resource on Keros website.
  • Parent Project Muscular DystrophyminorOthersPatient advocacy organization for Duchenne muscular dystrophy, listed as a patient resource on Keros website.
  • Treat-NMD Neuromuscular NetworkminorOthersInternational patient advocacy network for neuromuscular diseases, listed as a patient resource on Keros website.

Scale indicators11 records

Recent moves10 records

Expansion highlights4 records

Keros Therapeutics competitors and assessment

Company assessment

Direct peers

  • Acceleron Pharma: Founded by Keros CEO Jasbir Seehra, Acceleron pioneered the activin receptor ligand-trap approach (luspatercept/Reblozyl, sotatercept) and was acquired by Merck for ~$11.5B. Closest platform analog and direct precedent for the value of Keros' TGF-β assets.
  • Scholar Rock: Clinical-stage biotech developing apitegromab, a myostatin-activating antibody for SMA — directly targets the same TGF-β / myostatin axis Keros is pursuing with KER-065 in DMD and ALS.
  • Sarepta Therapeutics: Established DMD franchise (Elevidys gene therapy, EXONDYS 51, VYONDYS 53). Defines the competitive standard and pricing precedent for any DMD therapy including KER-065.
  • BioMarin Pharmaceutical: Developed and commercialized the first DMD therapy (drisapersen program) and operates a rare-hematology/rare-disease commercial platform. Keros Chairman Jean-Jacques Bienaime is BioMarin's former CEO/Chair.

Broad incumbents

  • Bristol Myers Squibb: Markets Reblozyl (luspatercept), an activin receptor Fc fusion approved in lower-risk MDS — the most direct competitive and mechanistic overlap with elritercept. BMS sets the benchmark Keros must beat in MDS.

Emerging players

  • Geron Corporation: Late-stage biotech with imetelstat approved in lower-risk MDS — competing for the same prescriber base as elritercept in MDS, making it a relevant adjacent competitor in Keros' core indication.
  • FibroGen: Clinical-stage rare-disease biotech (roxadustat, pamrevlumab) with comparable size, clinical-stage profile and rare-disease focus. Useful comparator for Keros' market cap and burn dynamics.
  • Disc Medicine: Clinical-stage hematology biotech focused on rare anemias and disorders of ineffective erythropoiesis — overlapping therapeutic area with Keros' elritercept MDS/MF program.
  • Ionis Pharmaceuticals: Antisense oligonucleotide platform with neuromuscular programs (e.g., tofersen in SOD1-ALS). Direct overlap with Keros' ALS strategy via the Healey MyMatch program.
  • Catalyst Biosciences: Rare hematology biotech with pipeline assets targeting complement-mediated and bleeding disorders. Comparable clinical-stage rare-hematology profile to Keros' elritercept franchise.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Keros Therapeutics social profiles

Digital presence

Keros Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Keros Therapeutics leadership team

Management profile

Number of profiles

Profiles12 records

Keros Therapeutics funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors10 records

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

Keros 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 Keros Therapeutics

What does Keros Therapeutics do?

Keros Therapeutics is a clinical-stage biopharmaceutical company that discovers, develops, and commercializes novel therapeutics targeting the transforming growth factor-beta (TGF-β) superfamily signaling pathway. Its lead product candidates are elritercept (KER-050), an ActRIIA fusion protein for hematological disorders such as myelodysplastic syndromes (MDS) and myelofibrosis, and rinvatercept (KER-065), a selective activin receptor ligand trap for neuromuscular disorders including Duchenne muscular dystrophy (DMD) and amyotrophic lateral sclerosis (ALS). Elritercept has been licensed to Takeda for global commercialization outside mainland China, Hong Kong, and Macau.

Is Keros Therapeutics a public or private company?

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

When was Keros Therapeutics founded?

Keros Therapeutics was founded in 2015. It employs 101 to 250 people.

Where is Keros Therapeutics based?

Keros Therapeutics is headquartered in Lexington, United States, in the North America region.

How does Keros Therapeutics make money?

Two revenue lines are on record. License Agreement Revenue is the primary driver. The others are pharmaceutical Product Sales.

Who are Keros Therapeutics's main competitors?

Direct peers on record are Acceleron Pharma, Scholar Rock, Sarepta Therapeutics and BioMarin Pharmaceutical. Bristol Myers Squibb is listed as a broad incumbent. Emerging players are Geron Corporation, FibroGen, Disc Medicine, Ionis Pharmaceuticals and Catalyst Biosciences.

Does Keros Therapeutics have an API?

No public API is recorded for Keros Therapeutics.

What industry is Keros Therapeutics in?

Keros Therapeutics's product category is Clinical-stage biopharmaceuticals. Its primary akta.pro industry code is HLAIAIAA, Genetic & Genomic Rare Disease Therapeutics. Its NAICS code is 541714 and its SIC code is 2836.

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Live signals
Markets DailyReviewing Upstream Bio (NASDAQ:UPB) and Keros Therapeutics (NASDAQ:KROS)Upstream Bio beats Keros Therapeutics on 7 of 13 factors, including higher revenue and a lower price-to-earnings ratio. Analysts rate Upstream Bio more favorably with a higher consensus target price, implying greater upside.MarketBeatKeros Therapeutics (NASDAQ:KROS) Raised to "Sell" at Wall Street ZenWall Street Zen upgraded Keros Therapeutics from a strong sell to a sell rating. The company's consensus rating is Hold with an average target price of $20.50, and it reported a loss of $1.45 per share for the quarter. The board approved a $5 million stock buyback program.American Banking and Market NewsReviewing Upstream Bio (NASDAQ:UPB) & Keros Therapeutics (NASDAQ:KROS)Keros Therapeutics and Upstream Bio are compared on profitability, institutional ownership, and analyst ratings. Upstream Bio beats Keros on 7 of 13 factors, with a higher consensus price target and upside. Analysts favor Upstream Bio, citing its stronger rating and higher probable upside.American Banking and Market NewsMacroGenics (NASDAQ:MGNX) & Keros Therapeutics (NASDAQ:KROS) Head-To-Head SurveyKeros Therapeutics and MacroGenics are compared on profitability, earnings, risk, institutional ownership, valuation, and analyst ratings. Keros has higher revenue and earnings, a stronger consensus rating, and a higher upside target, while MacroGenics trades at a lower price-to-earnings ratio.Markets DailyKeros Therapeutics, Inc. (NASDAQ:KROS) Stock Has Consensus Target Price of $20.50 According to AnalystsAnalysts rate Keros Therapeutics a Hold with a $20.50 target price. Insider Lorena Raquel Lerner sold 3,568 shares at $10.29, and the company authorized a $5M share repurchase. The stock opened at $11.26 after missing Q2 earnings estimates.Markets DailyKeros Therapeutics (NASDAQ:KROS) vs. MacroGenics (NASDAQ:MGNX) Financial AnalysisKeros Therapeutics and MacroGenics are compared on analyst ratings, profitability, and valuation. Keros has a stronger consensus rating and higher upside, but MacroGenics is more profitable and cheaper. Keros's lead product KER-050 targets cytopenias, while MacroGenics's MARGENZA treats HER2-positive breast cancer.American Banking and Market NewsKeros Therapeutics, Inc. (NASDAQ:KROS) Receives Average Rating of “Hold” from BrokeragesKeros Therapeutics shares received an average 'Hold' rating from nine brokerages, with a one-year target price of $20.50. The company missed its Q2 earnings estimate with a loss of $1.45 per share, and its board initiated a $5 million stock repurchase plan. Analysts forecast a fiscal-year loss of $5.27 per share.BioSpaceKeros Therapeutics Announces the First Patient Dosing in the Phase 2 Clinical Trial Evaluating Rinvatercept in DMDKeros Therapeutics announced the first patient was dosed in its Phase 2 clinical trial of rinvatercept for Duchenne muscular dystrophy. The open-label trial assesses safety and tolerability in late-ambulatory and early non-ambulatory patients, with initial data expected in the first half of 2027.Markets DailyKeros Therapeutics (NASDAQ:KROS) to Buyback $5.00 million in Outstanding StockKeros Therapeutics' board approved a $5.00 million share repurchase program on September 9th, authorizing up to 2.3% of shares. Analysts have a consensus 'Hold' rating with an average price target of $20.50, and the stock traded at $11.31.BioSpaceKeros Therapeutics Announces $5 Million Share Repurchase AuthorizationKeros Therapeutics' board approved a $5 million share repurchase program after receiving a $20 million development milestone from Takeda for elritercept. The repurchase follows the first patient dosing in the ELRiSE MDS trial. The program is discretionary and may be modified or discontinued.