Biotech firm with obesity ambitions: We aim for an agreement within a few years

The Danish-founded biotech company Pila Pharma looks to secure a partnership or acquisition within the next few years. The short-term goal is to advance the development of a promising new drug candidate for the treatment of obesity and diabetes.

Pila Pharma, listed on the Nasdaq First North stock exchange in Stockholm, has set a clear strategy for the future: Within a few years, the company aims to be acquired by or partner with an industry player capable of furthering and realizing its research in obesity and other metabolic diseases using TRPV1 inhibitors. The goal is to ensure that Pila Pharma’s potential new weight-loss pill reaches the market as quickly as possible.

– We have a promising drug candidate with a completely different side effect profile compared to other treatments currently in development or on the market. Our ambition is to progress the candidate over the next few years and then hand it over to a larger player who can take it to the next level. The global market is in dire need of effective obesity treatments, particularly scalable pill-based solutions, and we believe we could have a role to play in this development, says CEO Gustav H. Gram, adding:

– Since our founders’ discovery in 1999 and the company’s founding in 2014, we have made significant progress and gathered data that suggests we are on the right track. The next major step is to establish proof of concept for weight loss. We are the only company working with this specific type of molecule—TRPV1 inhibitors—as a novel therapeutic approach to treating obesity and other metabolic diseases. If we succeed, I firmly believe we will emerge as a strong and attractive candidate for partnership or acquisition.

A Scalable Pill Solution with a Different Side Effect Profile

Pila Pharma was founded by former Novo Nordisk researcher Dorte X. Gram, who was the first researcher to identify the molecule that later became semaglutide—the active ingredient in Novo Nordisk’s blockbuster drugs Ozempic and Wegovy.

During her tenure at Novo Nordisk, she also discovered— blocking the TRPV1 receptor— could be a potential new mechanism for treating metabolic diseases. With the rise of GLP-1 treatments, Pila Pharma is entering a highly competitive market where unique advantages will determine success.

– In our research and development efforts, we are focused on generating clinical data on the safety and efficacy of XEN-D0501 for treating obesity and related conditions such as diabetes. Patients, physicians, and the industry are all seeking effective weight-loss treatments without common side effects such as nausea, vomiting, and diarrhea. If we can achieve this with an oral solution that can be scaled to meet market demand, we envision a future where more patients have better access to sustainable weight management options, says Dorte X. Gram. She elaborates:

– Approximately one-third of patients worldwide who use GLP-1 medications for severe obesity—such as Wegovy—discontinue treatment prematurely due to side effects, cost, and availability issues. If we can offer a scalable pill alternative based on small molecules, it will significantly improve accessibility and help patients adhere to their treatment plans.

A Major Opportunity for Pill-Based Obesity Treatments

Professor Jens Juul Holst from the Department of Biomedical Sciences at the University of Copenhagen was among the first to discover the GLP-1 hormone in 1986, which plays a key role in stimulating insulin secretion from the pancreas. Today, GLP-1 receptor agonists are used to treat type 2 diabetes and severe obesity.

He sees significant potential for pill-based obesity treatments in certain markets.

– In some parts of the world, injection-based treatments pose a challenge, making a pill a far more attractive option. This is particularly true in Asian and African markets, where needle phobia is widespread, creating an enormous market opportunity. This factor is highly relevant to pharmaceutical companies, many of which avoid investing in injectable drugs due to economic considerations, says Jens Juul Holst.

He also predicts that pricing will play a decisive role in the future:

– With several new drugs on the horizon, if they deliver on their promises, small-molecule pills are poised to become a major success. One key reason is that they can be sold at a significantly lower price point compared to biologic drugs, which require more complex manufacturing, says Jens Juul Holst.

The core asset of Pila Pharma is its TRPV1 inhibitor, XEN-D0501 – an orally administered tablet currently in Phase 2 clinical development. At the end of 2024, the company announced its engagement with regulatory authorities to define the optimal approach for its next clinical trial in obesity and diabetes.

Biotech Company secures multi-million investment to revolutionize the Market for sustainable aroma with a groundbreaking new technology

EvodiaBio has raised an investment of 7 million euros from both foreign and Danish investment funds, including EIFO and The March Group. The new capital will be used for both commercialization and expansion.

It is a new groundbreaking and sustainable method to produce natural aroma that form the cornerstone of EvodiaBio’s technology. It can improve the taste of non-alcoholic beer while reducing the use of natural resources and CO2 emissions.

With extra capital backing, the company aims to become a global leader in sustainable aroma development for the food industry and beyond.

“We are incredibly proud to have achieved this milestone. This funding round is an important step towards our vision of revolutionizing the food industry with sustainable and innovative solutions. With support from our investors and our strong team, we are ready to take EvodiaBio to new heights and make a significant impact on the global stage,” says Camilla Fenneberg, CEO of EvodiaBio

Natural and sustainable aromas through Precision Fermentation

Hops are one of the key ingredients that give beer its great taste, but like many of nature’s other resources, the aromatic plant is threatened by climate change. Production is declining, and quality is deteriorating. EvodiaBio has developed a technology using yeast and precision fermentation to produce sustainable aromas that create the taste of hops.

These aromas are initially launched for the beer industry, where they can improve the taste of non-alcoholic beer and partially replace aromatic hops, which are currently threatened by climate change.

High interest from breweries

The company is experiencing high interest from breweries, and the possibilities extend beyond non-alcoholic products. With fresh capital, commercialization and expansion can be accelerated, and in the long term, EvodiaBio aims to improve the taste of various types of beverages and other food products.

Behind the ambitious Danish startup stands a strong board with prominent profiles such as Flemming Besenbacher, former Chairman of Carlsberg, Andreas Fibig, former CEO of IFF, and Anne Cabotin, former SVP at Symrise.

“I am pleased that we have now completed an oversubscribed up-round enabling us to continue our journey to make non-alcoholic beer taste great and reinvent the aroma industry by providing new sustainable solutions. A big thanks go out to our existing and new investors for their confidence in EvodiaBio and belief in our journey ahead.” says Chairman of the Board Jarne Elleholm.

EvodiaBio, founded just three years ago, is supported by a strong international syndicate of investors consisting of Nordic Foodtech VC, the German flavor house Symrise, PINC – the venture arm of Paulig, Thia Ventures VC, Newtree Impact, Ananke Ventures Limited, EIFO, and The March Group.

EvodiaBio received early-stage financial support of 2 million euros from the Danish BioInnovation Institute, founded by the Novo Nordisk Foundation. The state investment fund sees great potential in companies working towards green transition.

“We are pleased to support the continued development of the Danish biosolutions ecosystem, which stands strong internationally. It is crucial that we contribute with risk-tolerant capital so that advanced research from universities can be commercialized and support the green transition, which EvodiaBio can pave the way for. We see great potential in their innovative product, which the strong team behind the company can take far, and we are pleased with the support from international investors,” says Johan Bitsch Nielsen, Investment Manager, Green Transition, EIFO.

Poolbeg Pharma signs AI deal with OneThree Biotech to identify new drug targets and treatments for RSV

Poolbeg Pharma (AIM: POLB, ‘Poolbeg’ or the ‘Company’) a clinical stage infectious disease pharmaceutical company with a capital light clinical model, has signed an agreement with OneThree Biotech, Inc. a biology-driven artificial intelligence (‘AI’) company, to identify new drug targets and treatments for Respiratory Syncytial Virus (‘RSV’).

 Under the terms of the transaction and as aligned with Poolbeg’s strategy, OneThree Biotech’s state-of-the-art AI analysis tools will identify drug assets which target immune-response pathways, have a higher probability of clinical success and have the potential to prevent and / or treat infectious diseases. The analysis will prioritise drugs with existing Phase I safety data, reducing spend and risk, which can feed into Poolbeg’s rapid, capital light clinical development strategy and its expanding pipeline of assets. The analysis is expected to commence in Q1 2022 with preliminary outputs from this work expected in H2 2022.

OneThree Biotech is a clinically validated AI company with a proven technology platform which integrates chemical, biological, and clinical data with cutting-edge computational tools to answer complex questions surrounding disease biology and drug discovery. The team at OneThree will work closely with Poolbeg’s scientific team to build a tailored AI analysis model which can leverage the unique insights of human challenge trial data to identify disease-relevant cell signalling pathways which could lead to novel drug targets. OneThree will receive milestone payments based on candidate development and royalties on the sale of products derived from this partnership.

The Company believe that this partnership with OneThree Biotech is the first time that AI analysis has been undertaken on RSV human challenge trial data and samples to identify new drug targets. The unique nature of human challenge trials to produce disease progression data with high precision is expected to revolutionise the insights generated from this analysis. Poolbeg’s lead asset POLB 001, which is progressing towards its first human challenge trial in June 2022, was identified using such disease progression data. However, by utilising AI the Company aims to identify more targets, quicker and more cost efficiently than previously possible without this technology. 

Poolbeg entered a partnership with Eurofins Genomics in October 2021 to complete RNA sequencing of Poolbeg’s RSV disease progression samples from human challenge trials. This work was a key step in Poolbeg advancing its AI analysis programme. This RSV discovery dataset has been specifically designed for incorporation into OneThree’s AI platform. The data sets within this project will leverage up to 140Gb of biological data per subject spread over baseline healthy measurements and the course of infection which is expected to unveil unprecedented insights.

RSV is a contagious virus that affects the respiratory tract of children and at-risk older adults; in severe cases, it can cause pneumonia and other life-threatening breathing difficulties. RSV is a significant public health threat affecting an estimated 50-million people annually, leading to 4 million global hospitalisations and up to 74,500 in-hospital deaths in children under the age of 5 years. An estimated 45% of these cases and deaths occur in new-born infants under the age of 6 months.

Jeremy Skillington, PhD, CEO of Poolbeg Pharma, said:

“OneThree Biotech’s AI analysis tools will allow us to break new ground in data-driven drug discovery, by allowing us to evaluate and interrogate human challenge trial data like never before. This is a key part of our growth strategy, as we’ll be able to identify and develop drugs in a more time and cost effective manner, compared with the traditional biotech model. It will enable us to identify potential new treatments which have a higher probability of clinical success and which can feed into our rapidly expanding pipeline in-line with our capital light model.

This will be the first time that AI tools will be used to analyse RSV human challenge trial disease progression data, which illustrates the significance of this deal as well as Poolbeg’s innovative model. We look forward to updating the market on the outputs from this cutting-edge AI analysis in due course.”

Neel S. Madhukar, PhD, co-founder and CEO of OneThree Biotech, said:

“At OneThree our mission has always been to unlock new therapeutic opportunities by understanding biology on a deeper level. The ability to combine our AI platform with the data and expertise from Poolbeg Pharma will enable just that, and create an opportunity to make meaningful progress in the treatment of infectious diseases.”

 

Brad Pryde, co-founder and COO of OneThree Biotech, concluded:

 

“We have been impressed with Poolbeg Pharma’s clear dedication towards using technology and data to create efficiencies in drug discovery and development. We’re excited to demonstrate the strength of this partnership as future developments arise.”