Developer docs
API playgroundTry for free, no card

Search company profiles

Verdiva Bio

Full company profile

uuid000061a

Namestring
Verdiva Bio
Legal namestring
Verdiva Bio Limited
Websiteurl
verdivabio.com
Company typeenum
Private
Founded yearint
2025
Descriptiontext

Verdiva Bio is a clinical-stage biopharmaceutical company headquartered in London, UK, focused on developing rationally engineered peptide therapies for obesity and cardiometabolic diseases. The company was launched in January 2025 with a $410M+ Series A financing — reported as the largest UK/EU Series A at the time — led by Forbion with participation from General Atlantic, RA Capital, OrbiMed, Logos, Lilly Asia Ventures, and LYFE Capital. Its pipeline is anchored by VRB-101 (oral ecnoglutide), a GLP-1 analog being evaluated in the EVOLVE-2 Phase 2b trial in adults with obesity, and is broadened by VRB-102 (injectable amylin), VRB-103 (oral amylin), and VRB-104 (a GLP-1/amylin co-agonist).

The company's core technology combines licensed global rights (ex-Greater China) to ecnoglutide from Sciwind Biosciences with its proprietary T2026 oral absorption enhancer, which is designed to enable oral delivery of peptide therapeutics that are otherwise limited to injectable administration. This positions Verdiva to compete in the rapidly growing obesity therapeutics market, where current standard-of-care options (e.g., semaglutide, tirzepatide) are predominantly injectable. The Sciwind licensing agreement, valued at up to $2.4B in milestones plus royalties, provides a non-dilutive capital pathway and a parallel development track in China while Verdiva executes US- and ex-China-focused clinical development.

Verdiva Bio is pre-revenue with no approved or marketed products. Its business model is centered on advancing its pipeline through clinical development toward either commercialization or future partnership/transaction events, with near-term value creation driven by clinical readouts (notably the EVOLVE-2 Phase 2b data) and pipeline progression. Leadership is led by CEO Khurem Farooq, whose prior companies Aiolos Bio and Gyroscope Therapeutics were both acquired by large pharmaceutical companies, and the broader team draws from Genentech, GSK, and Novo Nordisk. The company was named to the 2025 Fierce Biotech Fierce 15 list, reflecting third-party recognition in a highly competitive therapeutic category.

Short descriptiontext

Verdiva Bio is a clinical-stage UK biopharmaceutical company developing rationally engineered oral and injectable peptide therapies for obesity and cardiometabolic disease, with lead asset VRB-101 (oral ecnoglutide) in Phase 2 and a broader amylin pipeline enabled by its proprietary T2026 oral absorption enhancer.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLondon, United Kingdom
HQ citystring
London
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Keyword5 values
obesity therapeutics, cardiometabolic drug development, peptide drug candidates, GLP-1 receptor agonists, clinical-stage biopharmaceutical
Industry2 codes
1Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity)
CodeHLAIAAAEPrimaryYes
2Cardiology & Vascular Specialty Pharmaceuticals
CodeHLAIACAGPrimaryNo
NAICS code2 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Cardiometabolic Biopharmaceuticals
Social media profiles1 record
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model2 records
1Pre-revenue Clinical Development
TypeLicensing Royalties
Description

Clinical-stage biotech company with no products currently approved or marketed. No recurring revenue. Future revenue expected from out-licensing arrangements and/or commercialization of cardiometabolic pipeline assets.

verdivabio.com
2Licensing Agreement with Sciwind Biosciences
TypeLicensing Royalties
Description

Global licensing agreement with Sciwind Biosciences valued at up to $2.4 billion for worldwide development of ecnoglutide and amylin candidates (VRB-101, VRB-103, VRB-104). Includes upfront, milestones, and potential royalties.

springernature.com
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

Verdiva Bio is a clinical-stage biopharmaceutical company developing rationally engineered peptide drug candidates for obesity and related cardiometabolic diseases. Its pipeline centers on oral and injectable once-weekly therapies, anchored by lead program VRB-101 (oral ecnoglutide, a cAMP-biased GLP-1 peptide analog in Phase 2) and an amylin-based portfolio (VRB-103, VRB-102, VRB-104), enabled by the proprietary T2026 oral absorption enhancer.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Verdiva Bio is a clinical-stage cardiometabolic biopharmaceutical company developing a portfolio of rationally engineered peptide drug candidates for obesity and related metabolic diseases, rather than a single unified product. The portfolio is anchored by the lead oral GLP-1 program VRB-101 (an oral formulation of ecnoglutide, a cAMP-biased GLP-1 peptide analog, in Phase 2 development using the proprietary oral absorption enhancer T2026) and expanded by an amylin franchise comprising the oral selective amylin analog VRB-103, the injectable amylin analog VRB-102 (intended for co-formulation with incretins such as VRB-101), and the unimolecular GLP-1/amylin co-agonist VRB-104. The named products are organized as distinct monotherapy and combination product candidates (for example, the once-weekly oral combination VRB-101 + VRB-103 and the injectable combination VRB-101 + VRB-102) that share common peptide-engineering and formulation science to enable both oral and injectable once-weekly dosing formats.

Product and service5 records
1VRB-101 (Oral Ecnoglutide)
CategoryLead pipeline candidate (oral GLP-1 peptide analog)
Description

Oral formulation of ecnoglutide, a cAMP-biased GLP-1 peptide analog in clinical development as a once-weekly treatment of obesity; enabled by the proprietary T2026 oral absorption enhancer and licensed from Sciwind Biosciences for worldwide development.

2VRB-103 (Oral Amylin Analog)
CategoryPipeline candidate (oral amylin analog)
Description

Oral, selective amylin analog in preclinical development as a once-weekly treatment of obesity, designed for use as monotherapy or in combination with oral GLP-1 therapy.

3VRB-101 + VRB-103 (Oral Combination)
CategoryPipeline combination candidate (oral GLP-1 + amylin)
Description

Once-weekly oral combination therapy pairing the GLP-1 analog VRB-101 with the selective amylin analog VRB-103, being evaluated as a once-weekly therapy for the treatment of obesity.

4VRB-101 + VRB-102 (Injectable Combination)
CategoryPipeline combination candidate (injectable GLP-1 + amylin)
Description

Injectable combination in which VRB-102, an amylin analog in preclinical development, is designed for co-formulation with incretins such as VRB-101 and for once-weekly injection to treat obesity.

5VRB-104 (Injectable GLP-1/Amylin Co-agonist)
CategoryPipeline candidate (injectable GLP-1/amylin co-agonist)
Description

Investigational unimolecular GLP-1 plus amylin co-agonist in preclinical development as a once-weekly injectable therapy for obesity; preclinical data showed 14% body weight loss over 14 days in a diet-induced obesity model versus 1% weight gain for vehicle.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biotech developing oral small-molecule and peptide GLP-1 agonists for obesity and cardiometabolic disease, including an oral once-daily GLP-1 in Phase 2. Most directly comparable peer to Verdiva's VRB-101 oral GLP-101 strategy.

TypeDirect peer
Description

Emerging clinical-stage obesity biotech developing oral and injectable peptide-based incretin and amylin analogs. Closely comparable to Verdiva in modality (oral peptides), mechanism (GLP-1/amylin), and obesity focus.

TypeDirect peer
Description

Obesity-focused biotech with a pipeline of injectable and oral GLP-1/amylin-based candidates. Directly comparable to Verdiva's combination amylin strategy and obesity-only positioning.

TypeDirect peer
Description

Clinical-stage biotech developing oral GLP-1 receptor agonists for obesity alongside an oncology pipeline. Closely tied to the Sciwind Biosciences ecosystem (founded by Verdiva CSO Weidong Zhong) and a direct peer in oral GLP-1 development.

TypeEmerging player
Description

China-based originator of ecnoglutide and the amylin candidates in-licensed by Verdiva. Comparable technology platform for oral peptide biologics and a key upstream licensor rather than a direct commercial competitor.

TypeEmerging player
Description

Clinical-stage cardiometabolic biotech developing controlled metabolic accelerators (HU6) for obesity and related metabolic disease. Comparable as a focused cardiometabolic/obesity clinical-stage peer with novel mechanism positioning.

TypeBroad incumbent
Description

Dominant incumbent in obesity and cardiometabolic with Mounjaro/Zepbound (tirzepatide), retatrutide, and oral orforglipron in late-stage development. Defines the competitive benchmark Verdiva must beat on efficacy, tolerability, and convenience.

TypeBroad incumbent
Description

Global incumbent in obesity and diabetes with Wegovy/Ozempic (semaglutide) and an advancing oral semaglutide program. Sets the standard of care against which Verdiva's VRB-101 oral GLP-1 will be evaluated.

TypeBroad incumbent
Description

Major pharmaceutical incumbent that re-entered the obesity space with danuglipron and has actively pursued oral GLP-1 development. Represents one of the strategic-acquisition or partnership counterparties Verdiva may eventually face.

TypeBroad incumbent
Description

Large pharmaceutical incumbent with a cardiometabolic franchise spanning diabetes, kidney, and obesity (including a survodutide collaboration with Zealand Pharma). Relevant incumbent peer and a potential strategic partner given CMO Mohamed Eid's prior tenure there.

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 risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 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 rounds1 record

Each record includes

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

Investors7 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 →

Verdiva Bio

Cardiometabolic Biopharmaceuticalsverdivabio.com

Verdiva Bio is a clinical-stage UK biopharmaceutical company developing rationally engineered oral and injectable peptide therapies for obesity and cardiometabolic disease, with lead asset VRB-101 (oral ecnoglutide) in Phase 2 and a broader amylin pipeline enabled by its proprietary T2026 oral absorption enhancer.

What Verdiva Bio does

Verdiva Bio is a clinical-stage biopharmaceutical company headquartered in London, UK, focused on developing rationally engineered peptide therapies for obesity and cardiometabolic diseases. The company was launched in January 2025 with a $410M+ Series A financing — reported as the largest UK/EU Series A at the time — led by Forbion with participation from General Atlantic, RA Capital, OrbiMed, Logos, Lilly Asia Ventures, and LYFE Capital. Its pipeline is anchored by VRB-101 (oral ecnoglutide), a GLP-1 analog being evaluated in the EVOLVE-2 Phase 2b trial in adults with obesity, and is broadened by VRB-102 (injectable amylin), VRB-103 (oral amylin), and VRB-104 (a GLP-1/amylin co-agonist).

The company's core technology combines licensed global rights (ex-Greater China) to ecnoglutide from Sciwind Biosciences with its proprietary T2026 oral absorption enhancer, which is designed to enable oral delivery of peptide therapeutics that are otherwise limited to injectable administration. This positions Verdiva to compete in the rapidly growing obesity therapeutics market, where current standard-of-care options (e.g., semaglutide, tirzepatide) are predominantly injectable. The Sciwind licensing agreement, valued at up to $2.4B in milestones plus royalties, provides a non-dilutive capital pathway and a parallel development track in China while Verdiva executes US- and ex-China-focused clinical development.

Verdiva Bio is pre-revenue with no approved or marketed products. Its business model is centered on advancing its pipeline through clinical development toward either commercialization or future partnership/transaction events, with near-term value creation driven by clinical readouts (notably the EVOLVE-2 Phase 2b data) and pipeline progression. Leadership is led by CEO Khurem Farooq, whose prior companies Aiolos Bio and Gyroscope Therapeutics were both acquired by large pharmaceutical companies, and the broader team draws from Genentech, GSK, and Novo Nordisk. The company was named to the 2025 Fierce Biotech Fierce 15 list, reflecting third-party recognition in a highly competitive therapeutic category.

Verdiva Bio firmographics

Firmographics
Name
Verdiva Bio
Legal name
Verdiva Bio Limited
Website
https://verdivabio.com
Company type
Private
Founded year
2025
Operating status
Operating
Headcount range
11–50 employees
Short description
Verdiva Bio is a clinical-stage UK biopharmaceutical company developing rationally engineered oral and injectable peptide therapies for obesity and cardiometabolic disease, with lead asset VRB-101 (oral ecnoglutide) in Phase 2 and a broader amylin pipeline enabled by its proprietary T2026 oral absorption enhancer.
Ownership category
akta.pro rank

Verdiva Bio industry classification

Industry
Product category
Cardiometabolic Biopharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (3254), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity) (HLAIAAAE)
akta.pro secondary industry
Cardiology & Vascular Specialty Pharmaceuticals (HLAIACAG)

Keywords

  • Obesity therapeutics
  • Cardiometabolic drug development
  • Peptide drug candidates
  • GLP-1 receptor agonists
  • Clinical-stage biopharmaceutical

Where Verdiva Bio is headquartered

Location

Headquarters

HQ city
London
HQ country
United Kingdom
HQ region
Europe

Markets served

Verdiva Bio 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. Pre-revenue Clinical Development: Clinical-stage biotech company with no products currently approved or marketed. No recurring revenue. Future revenue expected from out-licensing arrangements and/or commercialization of cardiometabolic pipeline assets.
  2. Licensing Agreement with Sciwind Biosciences: Global licensing agreement with Sciwind Biosciences valued at up to $2.4 billion for worldwide development of ecnoglutide and amylin candidates (VRB-101, VRB-103, VRB-104). Includes upfront, milestones, and potential royalties.

Go-to-market motion3 records

Verdiva Bio product offering

Product offering

Core offering

Verdiva Bio is a clinical-stage biopharmaceutical company developing rationally engineered peptide drug candidates for obesity and related cardiometabolic diseases. Its pipeline centers on oral and injectable once-weekly therapies, anchored by lead program VRB-101 (oral ecnoglutide, a cAMP-biased GLP-1 peptide analog in Phase 2) and an amylin-based portfolio (VRB-103, VRB-102, VRB-104), enabled by the proprietary T2026 oral absorption enhancer.

Product overview

Verdiva Bio is a clinical-stage cardiometabolic biopharmaceutical company developing a portfolio of rationally engineered peptide drug candidates for obesity and related metabolic diseases, rather than a single unified product. The portfolio is anchored by the lead oral GLP-1 program VRB-101 (an oral formulation of ecnoglutide, a cAMP-biased GLP-1 peptide analog, in Phase 2 development using the proprietary oral absorption enhancer T2026) and expanded by an amylin franchise comprising the oral selective amylin analog VRB-103, the injectable amylin analog VRB-102 (intended for co-formulation with incretins such as VRB-101), and the unimolecular GLP-1/amylin co-agonist VRB-104. The named products are organized as distinct monotherapy and combination product candidates (for example, the once-weekly oral combination VRB-101 + VRB-103 and the injectable combination VRB-101 + VRB-102) that share common peptide-engineering and formulation science to enable both oral and injectable once-weekly dosing formats.

Differentiator

Problem solved

Functional benefit

Products and services

  • VRB-101 (Oral Ecnoglutide) Oral formulation of ecnoglutide, a cAMP-biased GLP-1 peptide analog in clinical development as a once-weekly treatment of obesity; enabled by the proprietary T2026 oral absorption enhancer and licensed from Sciwind Biosciences for worldwide development.
  • VRB-103 (Oral Amylin Analog) Oral, selective amylin analog in preclinical development as a once-weekly treatment of obesity, designed for use as monotherapy or in combination with oral GLP-1 therapy.
  • VRB-101 + VRB-103 (Oral Combination) Once-weekly oral combination therapy pairing the GLP-1 analog VRB-101 with the selective amylin analog VRB-103, being evaluated as a once-weekly therapy for the treatment of obesity.
  • VRB-101 + VRB-102 (Injectable Combination) Injectable combination in which VRB-102, an amylin analog in preclinical development, is designed for co-formulation with incretins such as VRB-101 and for once-weekly injection to treat obesity.
  • VRB-104 (Injectable GLP-1/Amylin Co-agonist) Investigational unimolecular GLP-1 plus amylin co-agonist in preclinical development as a once-weekly injectable therapy for obesity; preclinical data showed 14% body weight loss over 14 days in a diet-induced obesity model versus 1% weight gain for vehicle.

Companies that use Verdiva Bio

Customer profile

Ideal customer profiles2 records

Verdiva Bio technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Verdiva Bio partnerships and signals

Strategic signal

Recent moves6 records

Expansion highlights4 records

Verdiva Bio competitors and assessment

Company assessment

Direct peers

  • Structure Therapeutics: Clinical-stage biotech developing oral small-molecule and peptide GLP-1 agonists for obesity and cardiometabolic disease, including an oral once-daily GLP-1 in Phase 2. Most directly comparable peer to Verdiva's VRB-101 oral GLP-101 strategy.
  • Metsera: Emerging clinical-stage obesity biotech developing oral and injectable peptide-based incretin and amylin analogs. Closely comparable to Verdiva in modality (oral peptides), mechanism (GLP-1/amylin), and obesity focus.
  • Kailera Therapeutics: Obesity-focused biotech with a pipeline of injectable and oral GLP-1/amylin-based candidates. Directly comparable to Verdiva's combination amylin strategy and obesity-only positioning.
  • Terns Pharmaceuticals: Clinical-stage biotech developing oral GLP-1 receptor agonists for obesity alongside an oncology pipeline. Closely tied to the Sciwind Biosciences ecosystem (founded by Verdiva CSO Weidong Zhong) and a direct peer in oral GLP-1 development.

Emerging players

  • Sciwind Biosciences: China-based originator of ecnoglutide and the amylin candidates in-licensed by Verdiva. Comparable technology platform for oral peptide biologics and a key upstream licensor rather than a direct commercial competitor.
  • Rivus Pharmaceuticals: Clinical-stage cardiometabolic biotech developing controlled metabolic accelerators (HU6) for obesity and related metabolic disease. Comparable as a focused cardiometabolic/obesity clinical-stage peer with novel mechanism positioning.

Broad incumbents

  • Eli Lilly: Dominant incumbent in obesity and cardiometabolic with Mounjaro/Zepbound (tirzepatide), retatrutide, and oral orforglipron in late-stage development. Defines the competitive benchmark Verdiva must beat on efficacy, tolerability, and convenience.
  • Novo Nordisk: Global incumbent in obesity and diabetes with Wegovy/Ozempic (semaglutide) and an advancing oral semaglutide program. Sets the standard of care against which Verdiva's VRB-101 oral GLP-1 will be evaluated.
  • Pfizer: Major pharmaceutical incumbent that re-entered the obesity space with danuglipron and has actively pursued oral GLP-1 development. Represents one of the strategic-acquisition or partnership counterparties Verdiva may eventually face.
  • Boehringer Ingelheim: Large pharmaceutical incumbent with a cardiometabolic franchise spanning diabetes, kidney, and obesity (including a survodutide collaboration with Zealand Pharma). Relevant incumbent peer and a potential strategic partner given CMO Mohamed Eid's prior tenure there.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks5 records

Key highlights7 records

Customer concentration

Verdiva Bio social profiles

Digital presence

Verdiva Bio financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Verdiva Bio leadership team

Management profile

Number of profiles

Profiles14 records

Verdiva Bio funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors7 records

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

Verdiva Bio 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 Verdiva Bio

What does Verdiva Bio do?

Verdiva Bio is a clinical-stage biopharmaceutical company developing rationally engineered peptide drug candidates for obesity and related cardiometabolic diseases. Its pipeline centers on oral and injectable once-weekly therapies, anchored by lead program VRB-101 (oral ecnoglutide, a cAMP-biased GLP-1 peptide analog in Phase 2) and an amylin-based portfolio (VRB-103, VRB-102, VRB-104), enabled by the proprietary T2026 oral absorption enhancer.

Is Verdiva Bio a public or private company?

Verdiva Bio is a private company. It is classified as venture growth investor backed and is currently operating.

When was Verdiva Bio founded?

Verdiva Bio was founded in 2025. It employs 11 to 50 people.

Where is Verdiva Bio based?

Verdiva Bio is headquartered in London, United Kingdom, in the Europe region.

How does Verdiva Bio make money?

Two revenue lines are on record. Pre-revenue Clinical Development is the primary driver. The others are licensing Agreement with Sciwind Biosciences.

Who are Verdiva Bio's main competitors?

Direct peers on record are Structure Therapeutics, Metsera, Kailera Therapeutics and Terns Pharmaceuticals. Emerging players are Sciwind Biosciences and Rivus Pharmaceuticals. Broad incumbents are Eli Lilly, Novo Nordisk, Pfizer and Boehringer Ingelheim.

Does Verdiva Bio have an API?

No public API is recorded for Verdiva Bio.

What industry is Verdiva Bio in?

Verdiva Bio's product category is Cardiometabolic Biopharmaceuticals. Its primary akta.pro industry code is HLAIAAAE, Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity), with a secondary code of HLAIACAG, Cardiology & Vascular Specialty Pharmaceuticals. Its NAICS code is 3254 and its SIC code is 2834.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
BioSpaceVerdiva ends mid-stage study of oral GLP-1 amid ‘market evolution’Verdiva Bio ended a Phase 2 study of its oral GLP-1 candidate VRB-101, citing market evolution, with no safety concerns. The study enrolled eight patients, and the biotech will continue developing the drug for other weight loss indications. It also plans to advance VRB-101 as monotherapy or in combination with its amylin assets.FierceBiotechDeep-pocketed Verdiva axes GLP-1 switching trial over ‘market evolution’Verdiva Bio terminated a phase 2 trial of its oral GLP-1 drug VRB-101 after enrolling eight participants, falling short of the 120 originally planned. The company cited market evolution and continues developing VRB-101 as a monotherapy, with Evolve-2 results expected by year-end.Business Wire BlogVerdiva Bio Presents Preclinical Data on VRB-103, a Selective Oral Amylin Peptide Analog, at 62nd EASD Annual MeetingVerdiva Bio presented preclinical data on VRB-103, a selective oral amylin peptide analog, at the EASD Annual Meeting. The data showed high potency and selectivity across amylin receptor subtypes versus comparators. VRB-103 is in Phase 1 as monotherapy and with VRB-101, with initial data anticipated by end of 2026.FinancialContent Business PageVerdiva Bio Initiates Phase 1 Study of VRB-103, a Selective Oral Amylin Peptide Analog With Weekly Dosing PotentialVerdiva Bio has initiated a Phase 1 clinical study with the first patient dosed for VRB-103, a once-weekly selective oral amylin analog being developed for the treatment of overweight and obesity. The randomized, double-blind, placebo-controlled study will evaluate VRB-103 as both monotherapy and in combination with VRB-101 (an oral GLP-1 analog) in healthy patients with elevated BMI, with initial data anticipated by the end of 2026. VRB-103 is described as the first known once-weekly, amylin receptor-selective oral amylin peptide analog currently in clinical development, leveraging Verdiva's proprietary oral peptide delivery platform.BioSpaceVerdiva Bio Initiates Phase 1 Study of VRB-103, a Selective Oral Amylin Peptide Analog With Weekly Dosing PotentialVerdiva Bio initiated a Phase 1 study of VRB-103, a once-weekly oral amylin analog, with the first patient dosed. The study evaluates VRB-103 alone and with VRB-101, with initial data anticipated by end of 2026. VRB-103 is the first known once-weekly oral amylin analog in clinical development.FierceBiotechChutes & Ladders—Biogen R&D vet gets in FormationThis article reports on multiple leadership changes across the biopharmaceutical industry, including Michael Ehlers joining Formation Bio as chief scientific officer and Steve Marso moving to Verdiva Bio as chief medical officer. It also details executive committee reshuffles at Sanofi and new CEO appointments at Mentari Therapeutics and Altesa BioSciences. Other noted moves include personnel changes at Neurocrine Biosciences, Tessera Therapeutics, and several other specialized biotech firms.The Pharma LetterVerdiva strengthens obesity team with former Metsera executivesVerdiva Bio appointed Steve Marso as chief medical officer and Jason Mallory as senior vice president of clinical development, both former Metsera executives. They will lead clinical strategy for Verdiva's once-weekly oral obesity candidates VRB-101 and VRB-103.BioSpaceVerdiva Bio Appoints Cardiometabolic Leader Steve Marso as Chief Medical OfficerVerdiva Bio appointed Steve Marso, M.D., as Chief Medical Officer and Jason Mallory as Senior Vice President Clinical Development, both joining from Metsera. Marso will lead clinical strategy for Verdiva's once-weekly oral obesity treatments, including VRB-103 and VRB-101, with VRB-101 in Phase 2.BioSpaceVerdiva Bio Presents Preclinical Data on Investigational Obesity Drug Candidates at the American Diabetes Association 86th Scientific SessionsVerdiva Bio presented preclinical data for VRB-103 and VRB-104 at the ADA 86th Scientific Sessions. VRB-103 showed high amylin receptor selectivity, while VRB-104 achieved 14% weight loss in an obesity model. VRB-103 is expected to enter the clinic in H2 2026.AijournVerdiva Bio Presents Preclinical Data on Investigational Obesity Drug Candidates at the American Diabetes Association 86th Scientific SessionsVerdiva Bio presented preclinical data on two investigational obesity drug candidates at the American Diabetes Association 86th Scientific Sessions in New Orleans. VRB-103 demonstrated higher potency and selectivity than eloralintide and cagrilintide across all three human amylin receptor subtypes, while VRB-104 achieved 14% body weight loss over 14 days in a diet-induced obesity model compared to 1% weight gain for vehicle. The company expects VRB-103 to enter clinical trials in H2 2026 as monotherapy and in combination with VRB-101, with both candidates licensed from Sciwind Biosciences for worldwide development.