The company is called NaDeNo and is well underway with the development of a new cure for cancers that have spread to the peritoneal cavity. It is a spin-off from SINTEF, where the technology was developed over a period of more than ten years within nanomedicine research.
The work from which NaDeNo has evolved started in 2012. Initial research at SINTEF yielded promising results, and now both the technology and its patents are being spun off from the research institute and into a separate company.
The technology makes it possible to embed large volumes of an active cancer drug in nanoparticle carriers. These carriers are then injected into the peritoneal cavity, enabling the drug to be evenly distributed and thus delivered to all the tumours developed in the peritoneum.
Delivering a large dose the tumours
Experiments using mice and rats demonstrate that the nanoparticles accumulate preferentially in the tumours, thus releasing a much greater proportion of the drug to cancer cells than they do to healthy cells.
“A solid foundation created by research carried out at SINTEF has enabled progress within the development of this technology”, says Ýrr Mørch, Chief Technology Officer (CTO) and co-founder at NaDeNo. “If we get the results we’re hoping for, the technology may represent a significant step forward, not only for the future treatment of peritoneal cancer, but also for other illnesses”, he says.
However, in order to make the technology accessible to cancer patients, it first has to be tested thoroughly and then manufactured at larger scales. It must be both safe and effective.
“We’re now getting ready to start pre-clinical trials”, says Mørch. “This phase will take some years, during which we will carry out a number of animal studies using standardised methods. We have to test the product thoroughly and also demonstrate that the drug is safe and can be manufactured with appropriate medical purity”, he says.
“The human body is composed mostly of water. Drugs that are poorly soluble in water are thus difficult to transport to the correct location in the body in sufficient doses to enable them to work for long enough to have their full effect without causing serious side effects.
The company will then apply to carry out clinical trials on cancer patients.
“Nanoparticles are now being manufactured at laboratory scale at SINTEF, but we have to show that we can produce these at an industrial scale”, says Mørch. “This must be carried out by specialist manufacturers, but to do this we have to go overseas”, he says. “A lot of research remains to be completed before the technology can be applied on cancer patients. We are still at an early phase”, he says.
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Results from experiments on a variety of tumours in mice have shown that just one injection of the new drug was sufficient to remove a targeted tumour. Stock photo: Shutterstock
Difficult to treat peritoneal cancer
Peritoneal cancer is difficult to discover and to treat. It often arises as a result of the spread of cancer cells from other organs such as the ovaries or digestive tract. It gives few symptoms and is often discovered too late. Survival prognoses are usually poor.
Current treatment approaches are yet to be standardised, and they tend to be life-extending rather than curative.
Patients who gets this diagnosis are commonly treated by surgical removal of all visible cancer tissue followed by chemotherapy that is administered either locally, or to the entire body via the blood. The problem with this approach is that the drug either has too short recidence time in the peritoneal cavity, or fails to reach the cavity and the cancer cells.
“This is due to a barrier that exists between the blood and the peritoneum”, says Annbjørg Falck, who is CEO and co-founder of NaDeNo.
In order for the drug to work effectively it has to be soluble in water. However, many chemotherapeutic treatments involve small-molecule drugs that are poorly soluble in water. Such treatments are thus difficult to deliver targeted at tumour sites.
Small particles with an enormous surface area
NaDeNo is aiming to address this by encapsulating the drug in tiny nanoparticle carriers. The nanoparticles are injected directly into the peritoneal cavity in a solution that ensures that they are distributed uniformly and reach all the tumours in the peritoneum. They then release the drug at the tumour sites.
“This drug is poorly soluble in water when it is ‘naked’ but becomes highly soluble when embedded in the nanocapsules developed by SINTEF”, says Mørch. “The capsules help the drug to reach the correct location. When the particles degrade in the body the drug is released”, she says.
Cabazitaxel is very powerful and exhibits less resistance development than other comparable cytotoxins. A new and optimised delivery method will thus enable many more patients to benefit from this effective drug.
In experiments with mice and rats, the researchers have observed that the nanoparticles accumulate in the tumours located in the peritoneum. This enables a greater proportion of the drug to reach the cancer cells and less is wasted on the healthy cells.
“The uniform distribution of the drug throughout the peritoneal cavity, combined with the longer residence time, demonstrates that the animals appear to tolerate the drug better when this delivery system is used”, says Mørch.
There are also other benefits.
“The size of the nanoparticles means that they have a large surface area in relation to their volume”, he says. “As many as 10¹² particles are contained in every millilitre of solution – literally billions of particles. This makes an enormous surface area available for interaction between the particles and their surroundings, and not least for attachment to the various cells and tissues in the human body”, says Mørch.
This enables the nanoparticles to deliver large amounts of the drug to the tumours.
NaDeNo is developing a technology by which small-molecule drugs that are normally difficult to deliver to body organs are embeded in tiny nanoparticle carriers. After injection, the nanoparticles carry the drug effectively to its target where the particles are degraded, gradually releasing the drug at the correct location. Diagram: SINTEF/NaDeNo
An effective anti-cancer cytotoxin
The product currently being developed by NaDeNo can thus be described as a nanotechnological platform for the encapsulation of non-water soluble (hydrophobic) drugs in nanoparticle carriers. There is currently great demand for the effective delivery of such drugs.
“If we succeed with our first product, it will enable us to offer a delivery technology that can benefit companies in both the pharmaceutical and biotechnology sectors”, says Mørch.
The cytotoxin that the company is using is called cabazitaxel. It is very effective, but current methods of delivery also cause major side effects.
“Cabazitaxel is currently used only for the treatment of prostate cancer”, says Annbjørg Falck. “The active component is highly toxic and is poorly soluble in water. For this reason, there are limits on how much of the drug can be administered without causing serious side effects”, she says.
The poor water solubility of cabazitaxel makes it difficult to develop nanoparticle delivery systems for the drug. NaDeNo thus has to demonstrate that embedding the drug in nanoparticles offers better efficacy compared to current treatments for patients suffering from cancer metastasis to the peritoneal cavity.
“Cabazitaxel is very powerful and exhibits less resistance development than other comparable cytotoxins”, says Falck. “A new and optimised delivery method will thus enable many more patients to benefit from this effective drug”, she says.
Diagram showing the anti-cancer cytotoxin cabazitaxel (in red) encapsulated in nanoparticle carriers. The material used to make the capsule (in green) is a degradable synthetic polymer. The same material is used to close wounds, since it will gradually degrad in the body. Diagram: SINTEF/NaDeNo
Multiple applications
Up until now, SINTEF’s development of its nanoparticle technology has been carried out in close collaboration with the Norwegian Radium Hospital in Oslo, with expertise in peritoneal cancer treatments.
This collaboration has provided NaDeNo’s first development candidate with a key clinical foundation and has enabled the company to obtain access to representative mouse models of human cancers, with very promising results.
“The Radium Hospital treats patients suffering from metastasis to the peritoneal cavity according to high international standards”, says Mørch. “The method is called hyperthermic intraperitoneal chemotherapy (HIPEC), where all visible tumour tissue is surgically removed from the cavity prior to local treatment with heated chemotherapy. In some cases, better efficacy is achieved by this methode. However, the treatment is very strenuous for the patients, who are very ill. The cytotoxin has a short residence time in the peritoneum and distributes rapidly to other parts of the body.
Kjersti Flatmark is a Professor and Senior Consultant in gastrosurgery at the Norwegian Radium Hospital and speaks very positively about the collaboration with NaDeNo and SINTEF.
“Metastasis to the peritoneum is difficult to treat and comes with a very poor prognosis. Unfortunately, our current treatment approaches very rarely cure our patients, so it is clearly a need for better treatment options. It has been exciting to be part of this collaborative effort, firstly with SINTEF and now with NaDeNo. Up to now we have focused on the development and testing of the technology in model systems, and are hoping that in the long term, the delivery of cytotoxins in nanoparticle carriers will contribute towards better treatment efficacy, enabling many more patients to enjoy a full recovery”, she says.
Initially, NaDeNo is focusing on a group comprising 37,000 patients annually in Europe and the USA. The company also has ambitions to apply the technology to a greater number of patients.
“If the first drug delivery system works, this will be a good indication that we have a technology that can be used for the treatment of many types of cancer that are currently difficult to treat”, says Mørch.
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Eyes on the market
SINTEF’s know-how in the design and characterisation of delivery platforms has made it an attractive partner both in Norway and across the world. From 2015 to 2020, SINTEF participated in the EU-funded European Nanomedicine Characterization Laboratory (EU-NCL) together with six European partners and the US National Cancer Institute (NCI).
In August 2022, NaDeNo’s first development candidate was accepted by the NCI as a promising nanomedicine. The NCI carries out a standardised preclinical test program free of charge, where the aim is to accelerate the development of nanomedicines that have the potential to treat patients with life-threatening diseases for which there is currently a pressing medical demand to find a cure.
“Inclusion in one of the NCI’s preclinical test programs is a key milestone for us, and offers valuable recognition of our development programme”, says Annbjørg Falck. The criteria for inclusion are quite strict, so this demonstrates that the work carried out by SINTEF over many years is of a high international standard”, she says.
Heidi Johnsen is a research manager for the team at SINTEF that participated in the development of the NaDeNo technology platform, and is optimistic for the future of the spin-off company.
“At SINTEF we work towards developing technology for a better society and I am proud of what we have achieved so far. We will continue to do the best we can in terms of effective collaboration to ensure that NaDeNo is successful with its product development”, she says.
“Our current strategy is to secure sound future investment with the aim of bringing our first product to the market and to patients, while at the same time continuing to develop our technological platform”, says Falck. “In this connection, we also want to forge links with partners in the biotechnology and pharmaceutical sectors that are looking for new and better ways of delivering poorly water-soluble drugs”, she concludes.
Facts about the company NaDeNo:
NaDeNo was founded in 2022 as a spin-off company from SINTEF. Its objective is to bring new nanomedicines to patients and to offer its drug delivery system to pharmaceutical and biotechnology companies.
The company’s current management team is composed of CEO and co-founder Annbjørg Eide Falck, who has an MBA and a master’s degree in pharmacy, and CTO and co-founder Ýrr Mørch, who has a PhD in biotechnology from NTNU and is one of the inventors of the technology.
The company’s key future milestones include the technical transfer and upscaling of its production processes to the status of ‘Good Manufacturing Practices (GMP)’, completion of the formal pre-clinical phase, and launch of the first clinical trials in cancer patients. The key partners who will help to achieve these milestones are SINTEF and the NCI Nanotechnology Characterization Laboratory (NCI-NCL) in the USA. The company also works closely with the Norwegian Radium Hospital in Oslo.
NaDeNo has recently completed its first round of capital raising. It has attracted financing from Norwegian investors both in Trondheim and elsewhere who have extensive experience of investing in SINTEF spin-offs. The company has also recently been granted an IPN (Innovation for Business) project funding by the Research Council of Norway. This is an important milestone that will enable the company to continue with its research, as well as the development of both its technology platform and innovative nanomedicines in close collaboration with SINTEF. Moreover, NaDeNo will continue to work to obtain additional ‘soft funding’ linked to the first product in its product portfolio.
