Gert W. Munthe, Chairman of the Board, and Øystein Rekdal, PhD, CEO of Lytix Biopharma. Photo: Håvar Haug

Lytix Biopharma signs licensing agreement

Our member Lytix Biopharma has entered into a milestone agreement with Verrica Pharmaceuticals to license the company’s lead drug candidate against skin cancer.

The Norwegian start-up Lytix Biopharma from Tromsø has reached a new milestone. The company has licensed its lead drug candidate LTX-315 against skin cancer to the dermatology therapeutics company Verrica Pharmaceuticals. Verrica Pharmaceuticals will develop and commercialize LTX-315 for dermatologic oncology indications.

The drug is a first-in-class oncolytic peptide-based immunotherapy. Immunotherapy is a type of cancer treatment that mobilises the patient’s own immune system to fight cancer. Peptides are short chains of between two and fifty amino acids that can have many different sources or functions. Peptides hold great potential for both cancer therapy and diagnostics, through the development of anticancer peptides, use of peptides for drug delivery, and cancer targeting.

Clinical studies have shown that the drug LTX-315 from Lytix Biopharma has the ability to kill human cancer cells and induce a specific anti-cancer immune response when injected locally into tumours.

“We are pleased to enter into this collaboration with Verrica, which has significant expertise within the field of dermatology” said Øystein Rekdal, CEO of Lytix Biopharma. “Our lead drug candidate, LTX-315, has shown very promising efficacy and safety signals in cancer patients during Phase I/II studies and we are excited that this partnership with Verrica will expand the applications for LTX-315”

The agreement entitles Lytix Biopharma to up-front payment, contingent regulatory milestones based on achievement of specified development goals, and sales milestones, with aggregate payments of more than $110M, as well as tiered royalty payments in the double-digit teens once Verrica successfully commercializes LTX-315 in dermatologic oncology indications.

Lytix Biopharma and Oslo Cancer Cluster

Lytix Biopharma has been a part of the innovation environment in Oslo Cancer Cluster Innovation Park since the building opened in 2015, utilising both offices and laboratory for research and development.

Oslo Cancer Cluster Incubator has offered the company its services in both private and shared laboratory spaces. In addition, Lytix Biopharma has been active in the animal laboratories at The Norwegian Radium Hospital (a part of Oslo University Hospital), which is located right next to the Incubator.

The researchers in Lytix Biopharma have gained their PhDs in the Incubator, in collaboration with its innovation environment. One of the company’s former researchers is now the laboratory manager in the Incubator.

“This shows how the innovation environments enrich one another in a positive sense, by sharing access to different services and thanks to the power of our geographic location,” said Bjørn Klem, general manager of Oslo Cancer Cluster Incubator.

Lytix Biopharma recently moved out of the Incubator after finishing their main project earlier this year and remains a member of Oslo Cancer Cluster.

Oslo Cancer Cluster Incubator is financed by SIVA, the Norwegian national infrastructure for innovation, consisting of incubators, business gardens, catapult centres, innovation enterprises, innovation centres and industrial real estate.

Sign up for our monthly newsletter to see the latest news and events

New member: Hemispherian

Image of Oslo Cancer Cluster Innovation Park

In this article series, we will introduce the new members of our oncology cluster.

Our newest member Hemispherian is developing a better treatment option for patients with aggressive brain cancer.

Glioblastoma multiforme is one of the most aggressive types of cancer that begins within the brain. Current treatment options are limited to surgery, radiotherapy and chemotherapy, the median overall survival after diagnosis is only 15 months and is highly dependent on the success of the surgery.

A Norwegian company called Hemispherian is advancing a new method to treat glioblastoma multiforme. The molecules the company is developing are called GLIX1 and GLIX5. They target a mechanism that is unique to cancer cells and does not affect normal healthy cells. The molecules are highly toxic to cancer cells and have minimal side effects.

We talked to Adam Robertson, Chief Scientific Officer in Hemispherian, to find out more about the company and the research.

How is Hemispherian involved in health and cancer?

“We are advancing first-in-class therapeutics for the indication with the greatest unmet need in oncology — glioblastoma multiforme. Patients diagnosed with glioblastoma multiforme have dismal outcomes. Overall survival is measured in months with quality of life deteriorating rapidly. It is Hemispherian’s mission to provide superior treatment options.” Adam Robertson, Chief Scientific Officer, Hemispherian.

Why did Hemispherian become a member of Oslo Cancer Cluster?

“As a company focusing on developing cancer treatments Oslo Cancer Cluster is a natural fit for us. We are interested in Oslo Cancer Cluster’s extensive experience in the field and hope to benefit from advice and to make valuable contacts through Oslo Cancer Cluster’s network.” Adam Robertson, Chief Scientific Officer, Hemispherian.

Researcher Anette Weyergang shows the PCI technology to Norwegian Prime Minister Erna Solberg.

Grants awarded for PDT/PCI research

Erna Solberg visits PCI Biotech

Radforsk has granted seven research projects a total amount of MNOK 1,25 to further develop exciting research projects within photodynamic treatment and photochemical internalization.

Radforsk is an evergreen investor focusing on companies that develop cancer treatments.

“Radforsk has ploughed NOK 200 million of its profit back into cancer research at Oslo University Hospital. Of these, NOK 25 million, have gone to research in PDT/PCI. This year we grant seven projects a total of NOK 1,25 million,” says Jónas Einarsson, CEO of Radforsk.

Radforsk had received a total of seven applications by the deadline on 1 March. All projects were allocated funding.

The applications have been assessed by external experts.

The researchers who have received funding for PDT/PCI research in 2020 are:

  • Anette Weyergang is granted NOK 300 000 to the project: “Photochemical Internalization: Development of a novel tumor-specific protein toxin to defeat aggressive and resistant cancers”
  • Beáta Grallert is granted NOK 100 000 for the project: “Cancer-specific bioluminescence-PDT”
  • Judith Jing Wen Wong is granted NOK 100 000 to the project “Light-enhanced targeting of immunosuppressive tumor cells”
  • Kirsten Sandvig and Tore Geir Iversen are granted NOK 200.000 to the project “Drug-loaded Photosensitizer-Chitoscan Nanoparticles for cominatorial Chemo- and Photodynamic cancer therapy”
  • Mouldy Sioud is granted NOK 200.00 to the project “Antibody- and peptide-targeted photodynamic therapy to kill cancer cells”
  • Qian Peng and Henry Hirschberg are granted NOK 50 500 to the project “Improved therapy of brain tumors by PDT induced anti-tumor immune responses”
  • Qian Peng is granted 300 000 to the project “Photopheresis of patients with Crohn’s disease using 5-aminolevulinic acid”

Read about the projects that were funded in 2019 here.

FACTS

PDT/PCI

Cancer research in the field of photodynamic therapy and photochemical internalisation studies the use of light in direct cancer treatment in combination with drugs, or to deliver drugs that can treat cancer to cells or organs.

Radforsk

Since its formation in 1986, Radforsk has generated NOK 600 million in fund assets and channelled NOK 200 million to cancer research, based on a loan of NOK 1 million in equity back in 1986.

During this period, NOK 200 million have found its way back to the researchers whose ideas Radforsk has helped to commercialise.

NOK 25 million have gone to research in photodynamic therapy (PDT) and photochemical internalisation (PCI). In total, NOK 40 million will be awarded to this research.

Rafiq Hasan has been appointed CEO of EXACT Therapeutics, a Norwegian company with a new technology that can enhance the effect of chemotherapy.

Combating cancer with ultrasound

CEO Rafiq Hasan, EXACT Therapeutics

Our member EXACT Therapeutics gains pharma veteran Rafiq Hasan as CEO, reveals company name change and reports strong progress in first clinical trial.

Our member EXACT Therapeutics, formerly known as Phoenix Solutions, is a Norwegian biotech company developing an innovative platform technology that enables precision therapeutic targeting using ultrasound, with an initial focus in oncology.

The method is called Acoustic Cluster Therapy (ACT®) and has potential utility across multiple therapeutic areas. In oncology, the effect of chemotherapy is amplified through biomechanical effects induced by ultrasound insonation of microbubbles transiently trapped in the microvasculature.

In other words, ACT® is a method to enhance the delivery of chemotherapy with greater precision exactly to the target site of action. Patients receive an intravenous injection of ACT® comprising microbubbles and microdroplets, which are activated at the location of the tumour using conventional diagnostic ultrasound. This creates large bubbles that apply transient and controlled pressure to the vascular wall enabling greater extravasation of the co-administered chemotherapeutic. In essence, this means that more chemotherapy is “pumped” into the tumour. The potential is that chemotherapy can achieve greater therapeutic efficacy using standard of care chemotherapy, resulting in better clinical outcomes for patients living with cancer.

Watch the video below to learn more about the technology in detail.

Pharma veteran appointed CEO

EXACT Therapeutics recently appointed Rafiq Hasan as CEO to lead the company on its journey to commercialise ACT. Rafiq Hasan is a seasoned veteran of the pharma business and has held several top positions in Bayer and Novartis.

Dr Hasan commented: “There has been tremendous progress in the last 8 years within the field of microbubbles and sonoporation, driven forward by ACT® and EXACT Therapeutics. Through its targeted delivery, ACT® has the potential to enhance therapeutic efficacy of a multitude of products across numerous therapeutic areas. This exciting science with the potential to have a transformative impact on medicine and patients, and I could not pass up this opportunity to lead EXACT Therapeutics into its next phase. I am impressed with the preclinical data where ACT® shows efficacy across a range of drugs and disease models, whilst the clinical development is already underway with the Royal Marsden Hospital/the Institute of Cancer Research.”

Clinical trial ongoing

EXACT Therapeutics is now reporting strong progress in an ongoing clinical trial, which started at the Royal Marsden Hospital in September 2019. The clinical trial is investigating ACT® in combination with standard of care chemotherapy for treating colorectal and pancreatic cancers.

Watch the video from BBC News of the first patient to test the new treatment.

Visit the original homepage to learn more about EXACT Therapeutics.

Sign up to our monthly newsletter