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Carmot Therapeutics

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uuid00008i4

Namestring
Carmot Therapeutics
Legal namestring
Carmot Therapeutics
Websiteurl
carmot.us
Company typeenum
Private
Founded yearint
2008
Descriptiontext

Carmot Therapeutics was a privately-held, clinical-stage biotechnology company headquartered in Berkeley, California, developing therapeutics for metabolic diseases with primary focus on obesity and diabetes. The company leveraged its proprietary Chemotype Evolution discovery platform to identify novel gut hormone-based drug candidates, with particular expertise in biased GLP-1 and GIP receptor agonist design intended to minimize β-arrestin recruitment and reduce receptor desensitization for prolonged pharmacological activity. Founded in 2008, Carmot operated with a lean headcount of 11–50 employees and was incorporated in Delaware.

Carmot's pipeline comprised three clinical-stage assets: CT-388/RG6640, a once-weekly subcutaneous injectable dual GLP-1/GIP receptor agonist in Phase 1b trials for obesity and type 2 diabetes; CT-868/RG6641, a GLP-1/GIP receptor agonist in Phase 2 trials for overweight/obesity and type 1 diabetes; and CT-996/RG6652, a once-daily oral small molecule GLP-1 receptor agonist in Phase 1 trials for obesity and type 2 diabetes. Each candidate was engineered with biased signaling properties to optimize cAMP-mediated efficacy while limiting receptor internalization. CT-388 Phase 2 results showed approximately 23 percentage points greater body weight loss versus placebo at 48 weeks.

As a pre-commercial R&D-stage biotech, Carmot generated no product revenue; its business model was venture-funded clinical development with monetization through strategic exit. The company raised approximately $310M across its Series D ($160M, July 2022, led by The Column Group) and Series E ($150M, May 2023, led by Deep Track Capital), following earlier rounds including a $47M Series C (September 2020, led by Amgen Ventures). In December 2023, Roche entered a definitive merger agreement to acquire Carmot for $2.7 billion, with the transaction closing in January 2024, integrating Carmot's pipeline and Chemotype Evolution platform into Roche's metabolic and obesity strategy targeting a market projected to exceed $100 billion annually.

Short descriptiontext

Carmot Therapeutics was a Berkeley-based, clinical-stage biotechnology company developing a portfolio of biased GLP-1/GIP dual agonists and an oral GLP-1 small molecule for obesity and diabetes using its proprietary Chemotype Evolution discovery platform. Acquired by Roche for $2.7 billion in December 2023.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBerkeley, United States
HQ citystring
Berkeley
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
metabolic disease therapeutics, GLP-1 receptor agonists, obesity drug development, diabetes treatment pipeline, incretin receptor modulators
Industry2 codes
1Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity)
CodeHLAIAAAEPrimaryYes
2Therapeutic Peptides & Protein/Peptide Biologics
CodeHLAAAAAHPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Metabolic Disease Therapeutics
Social media profiles2 records
Cost components3 values
Personnel, Technology or R&D, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1CT-388
Description

Once-weekly subcutaneous injectable, dual GLP-1/GIP receptor agonist being developed for the treatment of obesity and type 2 diabetes.

gene.com
+2 more records
Core offering1 text field

Carmot Therapeutics is a clinical-stage biotechnology company that discovers and develops therapeutics for metabolic diseases, with a focus on obesity and type 2 diabetes. Its core offerings are three clinical-stage drug candidates — CT-388, CT-868, and CT-996 — built on the company's proprietary Chemotype Evolution discovery platform and biased-signaling approach to GLP-1 and GIP receptor agonism.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Roche's CT-388 showed approximately 23 percentage points more body weight loss than placebo after 48 weeks in Phase 2 trials
Product overview1 text field

Carmot Therapeutics is a biotechnology company developing a portfolio of metabolic disease therapies focused on gut hormone modulation. The company's pipeline consists of three clinical-stage drug candidates: CT-868/RG6641 (GLP-1/GIP Receptor Agonist, Phase 2) for overweight/obesity and type 1 diabetes; CT-388/RG6640 (once-weekly GLP-1/GIP injectable, Phase 1b) for obesity and type 2 diabetes; and CT-996/RG6652 (once-daily oral GLP-1 agonist, Phase 1) for obesity and type 2 diabetes. These assets leverage dual incretin receptor modulation and biased signaling technology to optimize therapeutic efficacy while minimizing receptor desensitization. The company was acquired by Roche in December 2023 for $2.7 billion.

Product and service3 records
1CT-388 (RG6640)
CategoryMetabolic disease therapeutics — dual incretin receptor agonist
Description

CT-388 is a clinical-stage injectable peptide dual agonist of the GLP-1 and GIP receptors, developed for the treatment of obesity and type 2 diabetes. Following Roche's acquisition of Carmot, the asset is referred to as RG6640.

2CT-868 (RG6641)
CategoryMetabolic disease therapeutics — dual incretin receptor agonist
Description

CT-868 is a clinical-stage injectable dual GLP-1/GIP receptor agonist being developed for metabolic diseases including obesity and diabetes. Renamed RG6641 under Roche following the acquisition.

3CT-996 (RG6652)
CategoryMetabolic disease therapeutics — oral GLP-1 receptor agonist
Description

CT-996 is a clinical-stage oral small-molecule GLP-1 receptor agonist for the treatment of obesity and type 2 diabetes. Renamed RG6652 under Roche following the acquisition, it represents a non-injectable incretin option in the pipeline.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2023-12-04
Description

Roche acquired Carmot Therapeutics for $2.7 billion in December 2023, gaining access to three clinical-stage assets with best-in-class potential in obesity and diabetes (CT-388, CT-868, CT-996) and the Chemotype Evolution discovery platform. This acquisition positioned Roche to enter the metabolic and obesity market projected to exceed $100 billion annually.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers8 records
TypeBroad incumbent
Description

Eli Lilly markets tirzepatide (Mounjaro/Zepbound), the leading GLP-1/GIP dual agonist in obesity and type 2 diabetes, directly competing with Carmot's CT-388 and CT-868 mechanism and setting the efficacy bar Carmot's biased-agonist design must surpass.

TypeBroad incumbent
Description

Novo Nordisk markets semaglutide (Ozempic/Wegovy) and is developing next-generation incretin therapies; it is the dominant incumbent in the GLP-1 obesity/diabetes market that Carmot's pipeline is targeting.

TypeDirect peer
Description

Viking Therapeutics is a clinical-stage biotech developing VK2735, a dual GLP-1/GIP receptor agonist for obesity, directly competing with Carmot's CT-388 in the dual-incretin class with overlapping mechanism and patient population.

TypeDirect peer
Description

Structure Therapeutics is developing oral small-molecule GLP-1 receptor agonists (e.g., GSBR-1290), directly competing with Carmot's CT-996 in the oral GLP-1 space targeting obesity and type 2 diabetes.

TypeDirect peer
Description

Zealand Pharma develops peptide therapeutics for metabolic diseases, including petrelintide (amylin analog) and other incretin-based candidates, competing in the same obesity/metabolic disease space as Carmot's GLP-1/GIP portfolio.

TypeBroad incumbent
Description

Amgen is developing MariTide (maridebart cafraglutide), a GLP-1/GIP receptor agonist for obesity, positioning it as a direct competitor to Carmot's CT-388 in the dual-incretin class.

TypeBroad incumbent
Description

Pfizer is advancing oral GLP-1 candidates (e.g., danuglipron) for obesity and diabetes, directly competing with Carmot's CT-996 in the oral GLP-1 market segment.

TypeEmerging player
Description

Altimmune is developing pemvidutide, a GLP-1/glucagon dual agonist for obesity, representing an emerging competitor in the next-generation incretin space where Carmot's platform also operates.

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 risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment1 record

Each record includes

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

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

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 rounds8 records

Each record includes

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

Investors14 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 →

Carmot Therapeutics

Metabolic Disease Therapeuticscarmot.us

Carmot Therapeutics was a Berkeley-based, clinical-stage biotechnology company developing a portfolio of biased GLP-1/GIP dual agonists and an oral GLP-1 small molecule for obesity and diabetes using its proprietary Chemotype Evolution discovery platform. Acquired by Roche for $2.7 billion in December 2023.

What Carmot Therapeutics does

Carmot Therapeutics was a privately-held, clinical-stage biotechnology company headquartered in Berkeley, California, developing therapeutics for metabolic diseases with primary focus on obesity and diabetes. The company leveraged its proprietary Chemotype Evolution discovery platform to identify novel gut hormone-based drug candidates, with particular expertise in biased GLP-1 and GIP receptor agonist design intended to minimize β-arrestin recruitment and reduce receptor desensitization for prolonged pharmacological activity. Founded in 2008, Carmot operated with a lean headcount of 11–50 employees and was incorporated in Delaware.

Carmot's pipeline comprised three clinical-stage assets: CT-388/RG6640, a once-weekly subcutaneous injectable dual GLP-1/GIP receptor agonist in Phase 1b trials for obesity and type 2 diabetes; CT-868/RG6641, a GLP-1/GIP receptor agonist in Phase 2 trials for overweight/obesity and type 1 diabetes; and CT-996/RG6652, a once-daily oral small molecule GLP-1 receptor agonist in Phase 1 trials for obesity and type 2 diabetes. Each candidate was engineered with biased signaling properties to optimize cAMP-mediated efficacy while limiting receptor internalization. CT-388 Phase 2 results showed approximately 23 percentage points greater body weight loss versus placebo at 48 weeks.

As a pre-commercial R&D-stage biotech, Carmot generated no product revenue; its business model was venture-funded clinical development with monetization through strategic exit. The company raised approximately $310M across its Series D ($160M, July 2022, led by The Column Group) and Series E ($150M, May 2023, led by Deep Track Capital), following earlier rounds including a $47M Series C (September 2020, led by Amgen Ventures). In December 2023, Roche entered a definitive merger agreement to acquire Carmot for $2.7 billion, with the transaction closing in January 2024, integrating Carmot's pipeline and Chemotype Evolution platform into Roche's metabolic and obesity strategy targeting a market projected to exceed $100 billion annually.

Carmot Therapeutics firmographics

Firmographics
Name
Carmot Therapeutics
Legal name
Carmot Therapeutics
Website
https://carmot.us
Company type
Private
Founded year
2008
Operating status
Acquired
Headcount range
11–50 employees
Short description
Carmot Therapeutics was a Berkeley-based, clinical-stage biotechnology company developing a portfolio of biased GLP-1/GIP dual agonists and an oral GLP-1 small molecule for obesity and diabetes using its proprietary Chemotype Evolution discovery platform. Acquired by Roche for $2.7 billion in December 2023.
Ownership category
akta.pro rank

Carmot Therapeutics industry classification

Industry
Product category
Metabolic Disease Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity) (HLAIAAAE)
akta.pro secondary industry
Therapeutic Peptides & Protein/Peptide Biologics (HLAAAAAH)

Keywords

  • Metabolic disease therapeutics
  • GLP-1 receptor agonists
  • Obesity drug development
  • Diabetes treatment pipeline
  • Incretin receptor modulators

Where Carmot Therapeutics is headquartered

Location

Headquarters

HQ city
Berkeley
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Carmot Therapeutics business model

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

Carmot Therapeutics product offering

Product offering

Core offering

Carmot Therapeutics is a clinical-stage biotechnology company that discovers and develops therapeutics for metabolic diseases, with a focus on obesity and type 2 diabetes. Its core offerings are three clinical-stage drug candidates — CT-388, CT-868, and CT-996 — built on the company's proprietary Chemotype Evolution discovery platform and biased-signaling approach to GLP-1 and GIP receptor agonism.

Product overview

Carmot Therapeutics is a biotechnology company developing a portfolio of metabolic disease therapies focused on gut hormone modulation. The company's pipeline consists of three clinical-stage drug candidates: CT-868/RG6641 (GLP-1/GIP Receptor Agonist, Phase 2) for overweight/obesity and type 1 diabetes; CT-388/RG6640 (once-weekly GLP-1/GIP injectable, Phase 1b) for obesity and type 2 diabetes; and CT-996/RG6652 (once-daily oral GLP-1 agonist, Phase 1) for obesity and type 2 diabetes. These assets leverage dual incretin receptor modulation and biased signaling technology to optimize therapeutic efficacy while minimizing receptor desensitization. The company was acquired by Roche in December 2023 for $2.7 billion.

Differentiator

Problem solved

Functional benefit

Brands

  • CT-388: Once-weekly subcutaneous injectable, dual GLP-1/GIP receptor agonist being developed for the treatment of obesity and type 2 diabetes.
  • CT-868
  • CT-996

Products and services

  • CT-388 (RG6640) CT-388 is a clinical-stage injectable peptide dual agonist of the GLP-1 and GIP receptors, developed for the treatment of obesity and type 2 diabetes. Following Roche's acquisition of Carmot, the asset is referred to as RG6640.
  • CT-868 (RG6641) CT-868 is a clinical-stage injectable dual GLP-1/GIP receptor agonist being developed for metabolic diseases including obesity and diabetes. Renamed RG6641 under Roche following the acquisition.
  • CT-996 (RG6652) CT-996 is a clinical-stage oral small-molecule GLP-1 receptor agonist for the treatment of obesity and type 2 diabetes. Renamed RG6652 under Roche following the acquisition, it represents a non-injectable incretin option in the pipeline.

Quantifiable outcome

  • Roche's CT-388 showed approximately 23 percentage points more body weight loss than placebo after 48 weeks in Phase 2 trials

Companies that use Carmot Therapeutics

Customer profile

Segments1 record

Ideal customer profiles2 records

Carmot 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

Carmot Therapeutics partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • RocheflagshipStrategic or Co-development Partner · 4 December 2023Roche acquired Carmot Therapeutics for $2.7 billion in December 2023, gaining access to three clinical-stage assets with best-in-class potential in obesity and diabetes (CT-388, CT-868, CT-996) and the Chemotype Evolution discovery platform. This acquisition positioned Roche to enter the metabolic and obesity market projected to exceed $100 billion annually.

Scale indicators3 records

Recent moves6 records

Expansion highlights4 records

Carmot Therapeutics competitors and assessment

Company assessment

Broad incumbents

  • Eli Lilly: Eli Lilly markets tirzepatide (Mounjaro/Zepbound), the leading GLP-1/GIP dual agonist in obesity and type 2 diabetes, directly competing with Carmot's CT-388 and CT-868 mechanism and setting the efficacy bar Carmot's biased-agonist design must surpass.
  • Novo Nordisk: Novo Nordisk markets semaglutide (Ozempic/Wegovy) and is developing next-generation incretin therapies; it is the dominant incumbent in the GLP-1 obesity/diabetes market that Carmot's pipeline is targeting.
  • Amgen: Amgen is developing MariTide (maridebart cafraglutide), a GLP-1/GIP receptor agonist for obesity, positioning it as a direct competitor to Carmot's CT-388 in the dual-incretin class.
  • Pfizer: Pfizer is advancing oral GLP-1 candidates (e.g., danuglipron) for obesity and diabetes, directly competing with Carmot's CT-996 in the oral GLP-1 market segment.

Direct peers

  • Viking Therapeutics: Viking Therapeutics is a clinical-stage biotech developing VK2735, a dual GLP-1/GIP receptor agonist for obesity, directly competing with Carmot's CT-388 in the dual-incretin class with overlapping mechanism and patient population.
  • Structure Therapeutics: Structure Therapeutics is developing oral small-molecule GLP-1 receptor agonists (e.g., GSBR-1290), directly competing with Carmot's CT-996 in the oral GLP-1 space targeting obesity and type 2 diabetes.
  • Zealand Pharma: Zealand Pharma develops peptide therapeutics for metabolic diseases, including petrelintide (amylin analog) and other incretin-based candidates, competing in the same obesity/metabolic disease space as Carmot's GLP-1/GIP portfolio.

Emerging players

  • Altimmune: Altimmune is developing pemvidutide, a GLP-1/glucagon dual agonist for obesity, representing an emerging competitor in the next-generation incretin space where Carmot's platform also operates.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks5 records

Key highlights7 records

Customer concentration

Carmot Therapeutics social profiles

Digital presence

Carmot Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Carmot Therapeutics leadership team

Management profile

Number of profiles

Profiles1 record

Carmot Therapeutics funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors14 records

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

Carmot 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 Carmot Therapeutics

What does Carmot Therapeutics do?

Carmot Therapeutics is a clinical-stage biotechnology company that discovers and develops therapeutics for metabolic diseases, with a focus on obesity and type 2 diabetes. Its core offerings are three clinical-stage drug candidates — CT-388, CT-868, and CT-996 — built on the company's proprietary Chemotype Evolution discovery platform and biased-signaling approach to GLP-1 and GIP receptor agonism.

Is Carmot Therapeutics a public or private company?

Carmot Therapeutics is a private company. It is classified as corporate owned and is currently acquired.

When was Carmot Therapeutics founded?

Carmot Therapeutics was founded in 2008. It employs 11 to 50 people.

Where is Carmot Therapeutics based?

Carmot Therapeutics is headquartered in Berkeley, United States, in the North America region.

Who are Carmot Therapeutics's main competitors?

Broad incumbents on record are Eli Lilly, Novo Nordisk, Amgen and Pfizer. Direct peers are Viking Therapeutics, Structure Therapeutics and Zealand Pharma. Altimmune is listed as an emerging player.

Does Carmot Therapeutics have an API?

No public API is recorded for Carmot Therapeutics.

What industry is Carmot Therapeutics in?

Carmot Therapeutics's product category is Metabolic Disease Therapeutics. Its primary akta.pro industry code is HLAIAAAE, Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity), with a secondary code of HLAAAAAH, Therapeutic Peptides & Protein/Peptide Biologics. Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
Clinical Trials ArenaRoche’s acquired GLP-1/GIP normalises blood sugar in Phase II trialRoche's enicepatide met primary endpoints in a Phase II trial, normalizing blood sugar and reducing weight in type 2 diabetes patients. The 24mg dose lowered HbA1c by 2.65% and yielded 15.5% mean weight loss at 48 weeks. Roche plans Phase III trials in H1 2027.pharmaphorumRoche, Viking, and Syntis showcase obesity drug candidatesRoche, Viking Therapeutics, and Syntis reported new weight-loss drug candidates. Roche's enicepatide showed 15.5% weight loss and 2.65% HbA1c reduction at 24 mg; Viking's VK2735 achieved 17.7% weight loss at 21 weeks; Syntis's SYNT-101 was well tolerated with hormone changes. All companies plan further studies.SWI swissinfo.chRoche obesity shot reduced body weight by 15.5% in trialRoche's enicepatide shot cut body weight by 15.5% and HbA1c by 2.65% in a mid-stage trial of overweight or obese type-2 diabetes patients. The data is competitive with rivals, but Roche needs placebo-adjusted data and Phase 3 replication. Roche plans late-stage trials and expects approval by 2030.BusinessinsiderRoche logra una pérdida de peso del 15,5% con su nueva inyección contra la obesidadRoche's enicepatide injection reduced body weight by 15.5% and HbA1c by 2.65% in a phase 2b trial of type 2 diabetes patients. The company plans phase 3 trials in the first half of 2027, targeting a 2030 approval and $4 billion in sales.Labiotech.euRoche's strategy to reinvent its pipelineRoche is reinventing its pipeline with bets on obesity, IBD, and allogeneic cell therapy, including a $7.1 billion acquisition of Telavant and a $2.7 billion deal for Carmot. Its obesity lead CT-388 showed 22.5% weight loss in phase 2, but phase 3 trials face competition from Lilly and Novo Nordisk. Roche also faces Merck's earlier phase 3 results in IBD.GlobeNewswireGLP-1 Receptor Agonist Market Report 2026The GLP-1 receptor agonist market is projected to grow from $14.83 billion in 2026 to $18.32 billion by 2030 at a CAGR of 5.4%, driven by rising diabetes prevalence, obesity rates, and expanded approvals for cardiovascular risk reduction. Notable recent industry activity includes Roche's $2.7 billion acquisition of Carmot Therapeutics and Mitsubishi Tanabe Pharma Corporation's launch of Mounjaro as the first sustained-release dual GLP-1/GIP receptor agonist, reflecting intensifying competition among players including Novo Nordisk, Eli Lilly, and Sanofi. North America currently leads the market while Asia-Pacific is expected to be the fastest-growing region, with tariffs cited as a factor affecting pricing and supply chain diversification.openPR.comOutlook for the Type 2 Diabetes Market: Major Segments, Strategic Developments, and Leading CompaniesThe type 2 diabetes market is projected to reach $78.67 billion by 2030, growing at a compound annual growth rate of 9.1%, driven by rising demand for weight management therapies, personalized treatment plans, and digital therapeutic platforms. In January 2024, Roche Group acquired Carmot Therapeutics, gaining access to clinical and pre-clinical research assets and an innovative metabolism-focused discovery platform. In June 2024, AstraZeneca received U.S. FDA approval to expand its drug Farxiga for use in pediatric type 2 diabetes patients aged 10 years and older.openPR.comKey Companies Leading Innovation and Growth in the Type 2 Diabetes MarketThe global type 2 diabetes market is projected to reach $78.67 billion by 2030, growing at a compound annual growth rate of 9.1%, driven by increasing demand for weight management therapies, personalized treatment plans, and digital therapeutic platforms. In January 2024, Switzerland-based Roche Group acquired Carmot Therapeutics, gaining access to its R&D pipeline and the Chemotype Evolution discovery platform focused on obesity and diabetes treatments. In June 2024, UK-based AstraZeneca received U.S. FDA approval to expand its drug Farxiga for use in pediatric patients aged 10 years and older with type 2 diabetes.Phirda辉瑞和罗氏打起来了Pfizer and Roche are competing in the weight-loss drug market, with Pfizer acquiring Metsera and Roche developing Petrelintide. Pfizer's Ecnoglutide achieved 15.4% average weight loss in a Phase 3 trial, while Roche's Petrelintide showed 10.7% loss in a Phase 2 trial. Both companies aim to challenge Lilly and Novo Nordisk's dominance.BenzingaRoche's Obesity Drug Helps Almost 87% People Lose At Least 10% Weight - ROCHE HOLDING LTD S/ADR by RocheRoche Holdings AG released positive Phase 2 trial data showing its experimental obesity drug CT-388 achieved a placebo-adjusted weight loss of 22.5% over 48 weeks, with 87% of participants losing at least 10% of their body weight. The therapy, acquired through Roche's 2023 purchase of Carmot Therapeutics, has been designated a fast-track asset with Phase 3 trials expected to begin this quarter. The drug is positioned as a key component in Roche's strategy to compete with Eli Lilly and Novo Nordisk in the lucrative weight-loss drug market.