logo
#

Latest news with #VRB-103

Verdiva Bio to Present New Data Highlighting Once-Weekly Potential of Its Investigational Oral Obesity Candidates at the ADA 85th Scientific Sessions
Verdiva Bio to Present New Data Highlighting Once-Weekly Potential of Its Investigational Oral Obesity Candidates at the ADA 85th Scientific Sessions

Business Wire

time16 hours ago

  • Business
  • Business Wire

Verdiva Bio to Present New Data Highlighting Once-Weekly Potential of Its Investigational Oral Obesity Candidates at the ADA 85th Scientific Sessions

LONDON & SAN FRANCISCO--(BUSINESS WIRE)--Verdiva Bio Limited ('Verdiva' or 'the Company') a clinical-stage biopharmaceutical company focused on developing innovative therapies for obesity and cardiometabolic disorders, will present new data showcasing the once-weekly potential of Verdiva's investigational oral GLP-1RA and amylin analog peptide candidates at the American Diabetes Association (ADA) 85th Scientific Sessions. 'These presentations underscore the potential value of our compounds as the only once-weekly oral amylin and oral GLP-1 receptor agonist (RA) candidates known to be advancing into clinical studies," said Dr. Mohamed Eid, CMO, Verdiva Bio Share 'Our first data presentation as Verdiva Bio at the prestigious ADA meeting marks a key milestone for our team. These presentations underscore the potential value of our compounds as the only once-weekly oral amylin and oral GLP-1 receptor agonist (RA) candidates known to be advancing into clinical studies,' stated Dr. Mohamed Eid, CMO at Verdiva. 'The early clinical and preclinical data not only show the potential of these compounds individually, but also the additive effect they may have in combination, highlighting the flexibility of our modular portfolio approach. At Verdiva Bio, we are committed to developing convenient, patient-friendly and commercially scalable therapeutic options for obesity, cardiometabolic disorders and related complications. We're excited about the potential of our once-weekly oral peptide candidates to help address this global health challenge.' VRB-101: An investigational once-weekly oral GLP-1 analog This presentation highlights new clinical pharmacokinetic data for VRB-101, an investigational, once-weekly, cAMP-biased oral GLP-1RA formulated with Verdiva's clinically validated, proprietary oral delivery technology T2026. Phase 1 results demonstrated that oral VRB-101 achieved drug levels comparable to, or exceeding, those of currently available once-weekly injectable GLP-1RA therapies. These findings support continued investigation of VRB-101 as a potential once-weekly, scalable oral therapeutic option for both weight reduction and long-term weight maintenance, with the potential to exert potent weight reduction and may improve adherence via a more patient-friendly dosing regimen. Poster Presentation #069 Title: VRB-101 is a potent oral GLP-1 tablet with once-weekly dosing potential Date/Time: June 21, 2025, 12:30–1:30 p.m. Central Time Location: Poster Hall (Hall F1) 068, McCormick Place Convention Center VRB-103: Efficacy of novel once-weekly oral amylin analog as a monotherapy, and in combination with VRB-101 in vivo A second presentation will share novel preclinical data on VRB-103, an investigational potentially once-weekly oral amylin analog, tested alone and in combination with VRB-101. In preclinical models, the rationally designed peptide combination showed an additive effect on body weight reduction. Additionally, co-formulation of these peptides in a single tablet with T2026 maintained comparable plasma exposure for both compounds. These data support continued development of VRB-103 as both a monotherapy and in combination with VRB-101. Poster Presentation #068 Title: Efficacy of a novel oral amylin analog and the development of an oral GLP-1/amylin co-formulated tablet to produce high in vivo plasma exposures Date/Time: June 21, 2025, 12:30–1:30 p.m. Central Time Location: Poster Hall (Hall F1) 068, McCormick Place Convention Center About Verdiva Bio Verdiva Bio is committed to developing next-generation therapies to help people living with obesity, cardiometabolic disorders, and related complications achieve better outcomes via more patient-friendly therapeutic options. Verdiva's most advanced product candidate is VRB-101, an oral GLP-1 peptide in clinical development that has demonstrated potential efficacy in a phase 1 study in Australia, which also confirmed the viability of once-weekly dosing potential. The Company is also developing a portfolio of amylin molecules, including oral and subcutaneous agonists, and other undisclosed programs that offer the potential for enhanced efficacy and improved tolerability. The Verdiva team will harness the emerging science in gut-brain biology and leverage their history of successful drug development to advance novel therapeutic options aiming to transform the lives of millions living with obesity worldwide. For more information, please visit

Biopharma venture financing declines 20.2% YOY in Q1 2025 amid persistent investor caution
Biopharma venture financing declines 20.2% YOY in Q1 2025 amid persistent investor caution

Yahoo

time30-04-2025

  • Business
  • Yahoo

Biopharma venture financing declines 20.2% YOY in Q1 2025 amid persistent investor caution

Biopharmaceutical drug company venture financing witnessed a downturn in Q1 2025, with $6.5bn raised—a 20.2% decline from the $8.1bn raised in Q1 2024, according to GlobalData's Pharma Intelligence Center Deals Database. This suggests that the biopharmaceutical venture financing environment remains challenging, mirroring a similar downturn seen in 2022 and 2023, with investors continuing to favour later-stage companies with clinical data. Following a peak in 2021, biopharmaceutical venture financing witnessed a two-year decline that began in 2022. This downturn was driven by a wave of early-stage biotechs going public with inflated valuations, which led to a decline in investor confidence. Geopolitical challenges, rising inflation, and high interest rates further exacerbated this downturn, creating a more challenging funding environment. Signs of a recovery in biopharmaceutical venture financing emerged in 2024, characterised by an increase in total deal value and larger funding rounds. However, the momentum in venture financing activity was not sustained into Q1 2025, where a downturn was seen relative to Q1 2024, signalling persistent investor caution. Phase III biopharmaceutical companies recorded the highest median deal value at $62.5m, marking a 38.9% increase from $45m in 2021 despite a peak in overall venture financing activity that year (Figure 1). This reflects a shift towards investors committing larger amounts of capital towards companies nearing potential commercialisation—a trend observed since 2024. The largest venture financing deal reported in Q1 2025 was Isomorphic Labs, an AI biotech headquartered in London, which raised $600m. GlobalData's recent State of the Biopharmaceutical Industry 2025 report revealed that healthcare industry professionals ranked AI as the most impactful technology in the pharmaceutical industry. In January 2025, Verdiva Bio—another biotech headquartered in London—received $411m in series A financing towards the clinical development and expansion of its cardiometabolic portfolio. Verdiva Bio's portfolio comprises three drugs with rights outside of greater China and South Korea in-licensed from China-based company Sciwind Biosciences, including a 'Phase II ready' once-weekly oral GLPR agonist, VRB-101, as well as two preclinical amylin receptor agonists: oral VRB-103 and subcutaneous injectable VRB-102. To view further insights into venture financing activity globally in Q1 2025 in the pharma sector, please see our Pharma Venture Capital Investment Trends – Q1 2025 report. "Biopharma venture financing declines 20.2% YOY in Q1 2025 amid persistent investor caution" was originally created and published by Pharmaceutical Technology, a GlobalData owned brand. The information on this site has been included in good faith for general informational purposes only. It is not intended to amount to advice on which you should rely, and we give no representation, warranty or guarantee, whether express or implied as to its accuracy or completeness. You must obtain professional or specialist advice before taking, or refraining from, any action on the basis of the content on our site. Sign in to access your portfolio

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store