Our international Work

Oslo Cancer Cluster aims to enhance the visibility of oncology innovation made in Norway by being a significant partner for international clusters, global biopharma companies and academic centres.

– Our goal is to support our members in their effort to attract international partners, investments and successful academia-industry collaborations, says International Advisor Jutta Heix.

Heix is responsible for the cluster’s international initiatives, cluster network and partnering activities.

– Back in 2008, Oslo Cancer Cluster was not visible internationally, and few people knew about oncology innovation in Norway. We began to seek out partners and actively approach international pharma companies and other clusters offering relevant synergies, says Heix.


Building relationships abroad

The relationships thrive on joint initiatives. These include invitations to Norway with tailored programmes, where potential collaboration partners can meet academic teams, start-ups and biotechs. Oslo Cancer Cluster has also joined forces with other hubs and clusters internationally.

One such collaboration is the International Cancer Cluster Showcase (ICCS) at the global biotechnology gathering BIO International Convention in the US. In 2017, it is arranged for the 6th time, with European and North American partners, including the Massachusetts Technology Transfer Center, The Oncopole in Québec, The Wistar Institute in Philadelphia, Medicen in Paris and BioCat in Catalonia.

– This year the ICCS will showcase 24 innovative oncology companies from nine international innovation hubs and clusters. Three of our member companies in Oslo Cancer Cluster will use the opportunity to pitch their products and ideas to a global oncology audience, says Heix.

Jutta Heix is Oslo Cancer Cluster’s international advisor.


European and Nordic arenas
Meeting places are important in Europe too, with BIO-Europe, BIO-Europe Spring and Nordic Life Science Days at the top of the list. Oslo Cancer Cluster is the oncology partner at the Nordic Life Science Days. As a region, the Nordic countries are of international importance in the field of cancer research and innovation, especially in precision medicine, and Oslo Cancer Cluster participates in advancing Nordic collaboration.

Oslo Cancer Cluster also engages in more cancer specific European events. One example is the Association for Cancer Immunotherapy Meeting (CIMT), which is the largest European meeting in the field of cancer immunotherapy, also known as immuno-oncology.

– Many of our members are active in the field of immuno-oncology, so for a couple of years we have organized an event called CIMT Endeavour with German partners. The aim here is to discuss and promote translational research and innovation in immuno-oncology, says Heix.


Hot topics

Cancer immunotherapy has had a major impact on cancer treatment and global research and development in the cancer field. The concept took off with the approval of the first immune-checkpoint inhibitor, called Ipilimumab, in 2011. It offered a ground breaking new treatment for melanoma. In 2013, Science Magazine defined cancer immunotherapy as the breakthrough of the year. Since then, immunotherapy has been dominating the agenda of oncology meetings.

Other hot research and development topics are precision medicine and the increased digitization of the health sector. Oslo Cancer Cluster incorporates these topics in the international work, and aims to expand the services it provides for its members. The cluster recently got funding from Innovation Norway to do this, by adding an EU-advisor to the team.

– We want to increase our members’ involvement in EU’s research and innovation programme Horizon 2020. The new EU-advisor will help our members identify relevant funding schemes, find partners and prepare the applications, says Heix.

This initiative has already started to show some results. In the spring of 2017, Oslo Cancer Cluster member OncoImmunity AS won a prestigious Horizon 2020 SME Instrument grant, tailored for small and medium sized enterprises (SMEs). This grant targets innovative businesses with international ambitions — such as the bioinformatics company OncoImmunity.

 

New meeting places
– Member needs are important for us, as it is for clusters in general. Our network is for the benefit of our members. A good way of leveraging the network, is by creating relevant initiatives and new meeting places – to keep things moving forward, says Heix.

Oslo Cancer Cluster has new international initiatives coming up. One is in immuno-oncology, bringing Norwegian biotechs to the well-established research communities on the US East coast. The biotechs will get training and support, and will meet academic medical centres and biopharma companies in Boston and other cities. This initiative is supported by Innovation Norway’s Global Growth programme.

Another new initiative takes on academic innovation. More good ideas from academia should make it into patents, start-ups and investment opportunities for industry partners.

– Stanford University has a programme called SPARK. We are working with Norwegian partners, including The University of Oslo Life Science and The Norwegian Inflammation Network (NORIN), on implementing a Norwegian SPARK-programme. This will be part of the global SPARK-network, and we are already building a European node together with Berlin and Finland, Jutta Heix says.

OncoImmunity AS wins the EU SME Instrument grant

The bioinformatics company OncoImmunity AS was ranked fourth out of 250 applicants for this prestigious grant.

250 companies submitted proposals to the same topic call as OncoImmunity AS. Only six projects were funded.

We applied for the SME instrument grant as it represents an ideal vehicle for funding groundbreaking and innovative projects with a strong commercial focus. The call matched our ambition to position OncoImmunity as the leading supplier of neoantigen identification software in the personalised cancer vaccine market”, says Dr. Richard Stratford, Chief Executive Officer and Co-founder of OncoImmunity.


Personalised cancer vaccines
Neoantigen identification software facilitates effective patient selection for cancer immunotherapy, by identifying optimal immunogenic mutations (known as neoantigens). OncoImmunity develops proprietary machine-learning software for personalised cancer immunotherapy.

This solution also guides the design of neoantigen-based personalised cancer vaccines and cell therapies, and enables bespoke products to be developed faster.

The SME Instrument gives us the opportunity to further refine and optimise our machine-learning framework to facilitate personalised cancer vaccine design. This opportunity will help us establish the requisite quality assurance systems, certifications, and clinical validation with our partners, to get our software accredited as an in vitro diagnostic device”, says Dr. Richard Stratford.

In vitro diagnostics are tests that can detect diseases, conditions, or infections.

Dr. Richard Stratford is Chief Executive Officer and Co-founder of OncoImmunity, member of Oslo Cancer Cluster and part of the Oslo Cancer Cluster Incubator.


Hard to get
Horizon 2020’s SME Instrument is tailored for small and medium sized enterprises (SMEs). It targets innovative businesses with international ambitions — such as OncoImmunity.

“The SME instrument is an acid test; companies that pass the test are well suited to make their business global. It also represents a vital step on the way to building a world-class health industry in Norway”, says Mona Skaret, Head of Growth Companies and Clusters in Innovation Norway.

The SME Instrument has two application phases. Phase one awards the winning company 50 000 Euros based on an innovative project idea. Phase two is the actual implementation of the main project. In this phase, the applicant may receive between 1 and 2,5 million Euros.

The support from the SME instrument is proof that small, innovative Norwegian companies are able to succeed in the EU”, says Mona Skaret.

You can read more about the Horizon 2020 SME Instrument in Norwegian at the Enterprise Europe Network in Norway.

 

Thinking of applying?
Oslo Cancer Cluster helps its member companies with this kind of applications through the EU Advisor Program and close collaboration with Innovayt and Innovation Norway.

The SME Instrument is looking for high growth and highly innovative SMEs with global ambitions. They are developing innovative technologies that have the potential to disrupt the established value networks and existing markets.

Companies applying for the SME Instrument must meet the requirements set by the programme. Please see the SME Instrument website for more information.

Kick-Off: Call for Proposals for PERMIDES

The first call for proposals for the PERMIDES project is opening on March 15th. We urge all small and medium sized biopharma-companies working to take the step into the digital era, to apply for funding up to 60 000 Euros.

 

D.B.R.K Gupta Udatha, project manager for PERMIDES, is very happy to kick off the first call for proposals. He wants to help you succeed in this call for proposal by defining the essentials:

‘In your proposals, you should address the innovation barriers and challenges that you experience in the area of personalised medicine. It should be challenges that somehow can be solved by digitalisation’, says Udatha.

 

Developing novel personalised medicine
The voucher funding scheme of PERMIDES is aimed at small and medium sized enterprises (SMEs) from the biopharmaceutical sector developing novel personalised medicine products and solutions (e.g. biotech/medtech companies, diagnostics companies, CROs, biobank companies, bioinformatic companies).

‘To be eligible for funding, project teams must consist of one biopharma SME as the main applicant or beneficiary. In addition, there must be at least one IT SME as a service provider. Potential team partners in the project can be found via the PERMIDES platform, which offers a matchmaking of companies from the biopharmaceutical and IT sectors’, says Udatha.

 

Get more information:

 

Contact:

Jutta Heix, International Advisor
D.B.R.K Gupta Udatha, Project Manager PERMIDES

 

Kronikk i Aftenposten: De nordiske landene kan gjøre noe resten av verden drømmer om

De nordiske landene bør samarbeide mer for å utvikle bedre kreftbehandlinger. Sammen kan Norden bli et globalt forsknings- og testsenter for nye kreftbehandlinger og -medisiner. Det kan gi store gevinster for kreftpasienter i hele verden. Denne kronikken sto på trykk i Aftenposten torsdag 9. mars.

Ketil Widerberg, daglig leder i Oslo Cancer Cluster, skrev kronikken samme uke som The Economist, Forskningsrådet og Oslo Cancer Cluster arrangerte den nordiske konferansen War on Cancer Nordics i Oslo. De nordiske landene ønsker å lede an i kampen mot kreft. Nå er det på tide at infrastrukturer og lovverk legges til rette for det.


Norden kan vise vei i kampen mot kreft. For vi har noe de andre – selv ikke USA – har


Design, TV-serier og nå: kreft
Nordisk design er verdenskjent, og nordisk film har gjennom TV-serier som Broen etablert en ny sjanger i underholdningsindustrien. På 1990-tallet endret Nokia og Ericsson hvordan vi brukte mobiltelefonen. Slike fremskritt setter Norden på det internasjonale kartet og skaper arbeidsplasser. Nå er tiden inne for liknende fremskritt i kampen mot kreft. Vi har gode forutsetninger, men er vi vårt ansvar bevisst?

Vi har fremragende kreftforskning, for eksempel innen immunterapi for kreft, fotodynamisk teknologi og radioaktive legemidler (radiofarmaka). På disse områdene gjør både nordiske forskere og bioteknologifirmaer det godt internasjonalt. Hver for seg er de nordiske landene små, men samlet har de over 26 millioner innbyggere, og er et interessant marked for forskning, bioteknologi- og legemiddelselskaper.


Norden har unike fortrinn
Norden har flere forutsetninger for å lykkes. Først og fremst har alle nordiske borgere et unikt personnummer. Dette mangler faktisk i mange andre land, som USA. Personnummer har gjort det mulig for nordiske myndigheter å samle unike helsedata. I over 60 år har de nordiske landene samlet helse- og kreftdata i biobanker og registre og bygd verdensledende helsesystemer. Den nordiske befolkningen har dessuten et stort digitalt liv, og samfunnet har generell tillit til forskning.

De nordiske landene kan bruke disse felles fortrinnene til å gjøre noe resten av verden drømmer om: bruke offentlige helsedata for å se hvilken lovende medisin som virker på hver enkelt pasient. Slik kan legemiddelet godkjennes og tas i bruk før de tradisjonelle tidkrevende og kostbare delene av klinisk utprøving blir satt i gang. Tiden det tar fra et kreftlegemiddel blir patentert til det blir godkjent til bruk vil bli kortere, og pasienten vil kunne få behandlingen flere år tidligere. Samfunnet vil kunne spare millioner. Norden bør være seg sitt ansvar bevisst og gå i bresjen for raskere utvikling av ny kreftbehandling. Vi har ikke råd til å vente.


Ny viten gir bedre behandling
Kreft er en av vår tids store samfunnsutfordringer. Hvert år dør 8 millioner mennesker av kreft i verden og 14 millioner av oss får en kreftdiagnose. Det er mange, og antallet vil øke. Ifølge Verdens helseorganisasjon vil det øke med hele 70 prosent de neste 20 årene.

Heldigvis øker også forståelsen av hvor komplekse sykdommene som vi kaller kreft er. Vi vet at det finnes over 200 kreftsykdommer, og vi vet at kreft påvirkes blant annet av genetiske faktorer. I tillegg har vi nå forstått at immunsystemet spiller en viktige rolle i utviklingen av ulike kreftsykdommer og at vi kan påvirke immunsystemet til å spille på lag med kroppen mot kreften. Økt kunnskap om hva kreft egentlig er gir oss bedre forutsetninger for å vinne kampen mot kreft. Men med ny viten følger også en ny dynamikk for hvordan behandling skal utvikles, kategoriseres og tilbys pasienter.


Tid for politisk vilje
Digitalisering av kreftforskning gir rask fremgang i mange land. Store globale teknologifirmaer som Microsoft, IBM og Google satser nå på helse, og spesifikt kreft. Med kunstig intelligens kan kreftforskere simulere, teste hypoteser og samle og korrelere data som ikke var mulig for kun få år siden. Norden har unike helsedatabaser, og vi kan bygge opp kompetanse sammen med globale selskaper på samme måte som Norge bygde opp oljeindustrien på 1970-tallet. Da inviterte Norge inn store internasjonale selskaper som utviklet oljeindustrien under statlig styring. Dette krevde samarbeid og tilrettelegging fra det offentlige.

En satsing på et nordisk kreftsamarbeid krever også offentlig tilrettelegging. Myndighetene og offentlige instanser må åpne for at forskere kan få bruke helsedataene vi allerede har. I Norden har vi strukturen som gjør det mulig å nå raskere fram med ny forskning. Vi kan hjelpe pasienter ved å godkjenne og ta i bruk legemidler før de tradisjonelle tidkrevende og dyre siste kliniske studiene settes i gang. Både USA og EU har forsøkt, men med begrenset hell, blant annet fordi de mangler personnummer og har fragmenterte helsesystemer. Der har de politisk vilje, men mangler strukturene.


Et globalt testsenter
Nordiske helsevesen samler inn stadig mer data fra befolkningen. Nå kan slike helsedata brukes til å utvikle medisiner raskere. Det vil stille nye krav til rapportering, sikkerhet og formål med bruk av helsedata. Det vil kreve en åpen og innovativ holdning både fra offentlige og private aktører. Dette er ikke risikofritt, men gevinsten for samfunnet og for den enkelte pasient som overlever takket være raskere og bedre behandling, vil være betydelig.

Norden har en unik mulighet til å være et globalt testsenter for utvikling av nye legemidler som utnytter den offentlige digitale infrastrukturen. Google endret hvordan vi bruker internettet. Vi gikk fra AltaVista til Google, og så oss aldri tilbake. Norden har alle forutsetninger for å lede an i digitaliseringen innen helse. Det kan være med på å endre livet til de 14 millionene nye menneskene som får kreft hvert år.

Ketil Widerberg, daglig leder i Oslo Cancer Cluster

Targovax to present at upcoming conferences

Oslo, Norway, 6 March 2017: Targovax ASA (“Targovax” or “the Company”; OSE: TRVX), a clinical stage company focused on developing immuno-oncology therapies to target, primarily, treatment-resistant solid tumors, announces that members of its senior management will present at the following life sciences and investor conferences:

 

10th European Life Science CEO Forum (hosted by Sachs Associates)
Date: 7 March 2017
Venue: Hilton Zurich Airport Hotel, Zurich, Switzerland

Panel discussion time: 11:10 CET – Advances in Immuno-Oncology Therapeutics Panel

– Magnus Jäderberg (CMO)

Presentation time: 12:25 CET

– Øystein Soug (CEO)

 

Redeye – Fight Cancer Seminar
Date: 10 March 2017
Venue: Redeye, Stockholm, Sweden

Presentation time: 10:50 CET

Participants: Øystein Soug (CEO)

 

11th Annual BIO-Equity Spring 2017 Conference
Date: 20-22 March 2017
Venue: CCIB Convention Centre in Barcelona, Spain

Participants: Øystein Soug (CEO) and Peter Skorpil (VP Business Development)

 

The presentations will be available to download at www.targovax.com following these events.

 

For further information, please contact:

Renate Birkeli, Investor Relations

Phone: +47 922 61 624

Email: renate.birkeli@targovax.com

 

Media and IR enquires:

Jan Petter Stiff – Crux Advisers (Norway)

Phone: +47 995 13 891

Email: stiff@crux.no

 

Julia Phillips/Simon Conway – FTI Consulting (International)

Phone: +44 20 3727 1000

Email: Targovax@fticonsulting.com

 

About Targovax

Arming the patient’s immune system to fight cancer

Targovax is a clinical stage company focused on developing and commercializing novel immuno-oncology therapies to target, primarily, treatment-resistant solid tumors. Immuno-oncology is currently one of the fastest growing therapeutic fields in medicine.

The Company’s development pipeline is based on two novel proprietary platforms:

The first platform, ONCOS, uses oncolytic viruses, an emerging class of biological therapy. ONCOS exclusively uses an adenovirus that has been engineered to be a tumor-targeted immune activator. The platform has the potential to generate therapies with superior efficacy and safety compared to the first approved oncolytic virus therapy, Imlygic®, launched by Amgen. We continue to expect key proof of concept data for this platform in 2017 from a clinical study of lead program ONCOS-102 in patients with refractory malignant melanoma.

The second platform, TG-Peptides (TGP), solely targets tumors that express mutated forms of the RAS protein. Mutations to this protein are common in many cancers and are known to drive aggressive disease progression and treatment resistance. There is a high unmet medical need for therapies that are effective against tumors that express these mutations.  The TGP platform’s therapeutic potential stems from its ability to enable a patient’s immune system to identify and then destroy tumors bearing any RAS mutations. In early 2017, key proof of concept data for the TGP platform from a clinical study of TG01 in resected pancreatic cancer patients showed encouraging overall survival and will determine plans for the future clinical development of this platform.

Targovax’s development pipeline has three novel therapeutic candidates in clinical development covering six indications. Already promising safety and tolerability data and early signs of clinical response have been demonstrated.

Both platforms are protected by an extensive portfolio of IP and know-how and have the potential to yield multiple product candidates in a cost-effective manner. We have a number in early stages of development in addition to the three outlined above.

In July, 2016 the Company listed its shares on Oslo Axess.

This information is subject to the disclosure requirements pursuant to section 5-12 of the Norwegian Securities Trading Act.

The Economist & Oslo Cancer Cluster: War on Cancer Nordics

Oslo Cancer Cluster is proud to be partner of The Economist Events War On Cancer Nordics.

The War on Cancer Nordics 2017 in Oslo will gather leaders in oncology from the Nordic region and beyond, to discuss the region’s primary challenges in cancer care and control. The event will bring together policy makers, NGOs, academia, research and health care professionals, patient groups and cancer control institutes with private sector business leaders.

 

Questions we will answer

  • How much does cancer cost the Nordic countries per year both in terms of treatment costs and its impact on the labour market?
  • Would a unified Nordic oncology framework be desirable? 
  • What can be learnt from countries that have made more progress in prevention initiatives? 
  • How could research in immuno-oncology be scaled across the region to improve outcomes for patients? 
  • What role will new technologies play in shaking up cancer care, from prevention, through diagnosis, to treatment and to optimise symptoms and quality of life?

 

Founding sponsor: The Research Council og Norway and silver sponsor: Roche

Dehns is now member of the Oslo Cancer Cluster

Dehns Patent and Trade Mark Attorneys recently joined the Oslo Cancer Cluster.

Dehns is one of Europe’s largest firms of patent and trade mark attorneys and has a 40 year history of working with Norwegian organisations such as: Dynal, Inven2,Lytix Biopharma, Nextera, NMBU, NTNU, Nycomed, PCI Biotech and Photocure.

As members, our aim is to advise and help protect the other members needs regarding innovations and intellectual property (IP) around cancer research, diagnosis and treatment.

With experts in this field, many of whom also have PhDs, we can help you build and manage your IP portfolio and strategy, including providing advice on the patentability of inventions, draft and file patent applications, represent you in opposition and other contentious proceedings, as well as advise on academia-industry collaborations and licensing agreements.

www.dehns.com

 

Single-dose Betalutin® shows promising efficacy

Nordic Nanovector ASA presented the updated results from its ongoing Lymrit 37-01 Phase 1/2 clinical trial of Betalutin® (177Lu-satetraxetan-lilotomab) in subjects with relapsed non-Hodgkin lymphoma (NHL) at the 58th Annual American Society of Hematology (ASH) meeting (San Diego, CA, USA).

 

The updated data confirm Betalutin®’s promising efficacy and favourable safety profile as a single agent in 38 relapsed NHL patients, having failed multiple prior regimens and being eligible for assessments. The results, based on the data cut-off date of 31 October 2016, were presented by the study’s Principal Investigator Dr. Arne Kolstad from the Department of Oncology at the Oslo University Hospital, Radiumhospitalet.

Key conclusions:

• In the 35 patients evaluable for efficacy, the Overall Response Rate (ORR) was 63%, with 29% Complete Responses (CR)

• The 21 evaluable patients in the study who received Betalutin® at the dose of 15 MBq/kg with 40 mg/m2 lilotomab pre-dosing had an ORR of 62% and a CR of 38%; of these, the 16 patients enrolled in the Phase 2 expansion of Arm 1, had an ORR of 69% and a CR of 38%

• Durable responses have been observed with a median duration of response of 20.7 months for all patients in Arm 1

• Betalutin® is well tolerated, with a predictable and manageable safety profile: most adverse events are haematological in nature, and all have been transient and reversible

• No dose-limiting toxicity (DLT) was reported in Arm 4 (15 MBq/kg Betalutin® plus 100 mg/m2 lilotomab pre-dosing) and this regimen demonstrated lower bone marrow toxicity than Arm 1, 2 and 3. Arm 4 is now enrolling patients to evaluate the higher dosing regimen of 20 MBq/kg Betalutin® plus 100 mg/m2 lilotomab.

The Lymrit 37-01 study is a Phase 1/2 open label, dose escalation study investigating the optimal lilotomab pre-dosing and Betalutin® regimen in patients with relapsed NHL. Data from 38 patients are presented.

Dr. Arne Kolstad, MD commented -The results we are presenting today are very encouraging and continue to highlight the potential of Betalutin® to provide a new treatment option for NHL patients. These patients, particularly those who fail standard CD20-targeted immunotherapy and/or are too frail to receive chemotherapy, are desperately in need of alternative therapies that work through different and complementary mechanisms and are well tolerated. Betalutin® is showing exciting promise in an increasing number of NHL patients and we look forward to the results from future studies that will hopefully confirm its attractive profile.

Dr. Lisa Rojkjaer, MD Nordic Nanovector’s Chief Medical Officer, commented -These new data confirm the promising results for Betalutin®, including durable responses in a number of patients, which were presented earlier this year at the AACR meeting, and continue to demonstrate an encouraging clinical profile as a single agent for treating patients with relapsed NHL. The results also support escalating to a higher dosing regimen in the final stages of this Phase 1/2 study that will allow us to decide an optimal dosing regimen for the pivotal Phase 2 study, PARADIGME, expected in Q1 2017.

The poster (abstract 1780) was presented on Saturday, 3 December 2016 between 5:30PM–7:30PM Pacific Standard Time (Oslo: Sunday 4 December, 2:30AM–4:30AM CET) and is available at: http://www.nordicnanovector.com/product-info/scientific-posters.

 

 

About Nordic Nanovector
Nordic Nanovector is a biotech company focusing on the development and commercialisation of novel targeted therapeutics in haematology and oncology. The Company’s lead clinical-stage product opportunity is Betalutin®, the first in a new class of Antibody-Radionuclide-Conjugates (ARC) designed to improve upon and complement current options for the treatment of non-Hodgkin Lymphoma (NHL). NHL is an indication with substantial unmet medical need and orphan drug opportunities, representing a growing market worth over $12 billion by 2018.

Betalutin® comprises a tumour-seeking anti-CD37 antibody, lilotomab (previously referred to as HH1), conjugated to a low intensity radionuclide (lutetium-177). The preliminary data has shown promising efficacy and safety profile in an ongoing Phase 1/2 study in a difficult-to-treat NHL patient population. The Company is aiming at developing Betalutin® for the treatment of major types of NHL with first regulatory submission anticipated in 1H 2019.

Nordic Nanovector intends to retain marketing rights and to actively participate in the commercialisation of Betalutin® in core markets, while exploring potential distribution agreements in selected geographies. The Company is committed to developing its ARC pipeline to treat multiple selected cancer indications.

Further information about the Company can be found at www.nordicnanovector.com

This information is subject to the disclose requirements pursuant to section 5-12 of the Norwegian Securities Trading Act.

Photocure with good results

Oslo Cancer Cluster member Photocure ASA is a specialty pharmaceutical company focused on photodynamic technologies in cancer and dermatology. They reported a revenue growth of 17 % to NOK 31.6 million in the third quarter of 2016 (Q3 2015: NOK 27.0) for the Hexvix/Cysview commercial franchise and a corresponding EBITDA of NOK 8.0 million.

Watch full presentation here.

 

About:
Photocure, the world leader in photodynamic technology, is a Norwegian based specialty pharmaceutical company. They develop and commercialize highly selective and effective solutions in several disease areas such as bladder cancer, HPV and precancerous lesions of the cervix and acne.

Photocure currently have one product on the market: Hexvix®/Cysview® (The brand name is Cysview in the US and Hexvix in the rest of the world).

The Photocure Technology® is uniquely selective, targeting affected areas without impact to non-affected areas. This allows for non-invasive procedures that improve quality of life.

For more information on Photocure.

Cancer Crosslinks 2017

Det er med stor glede vi inviterer onkologer, hematologer og forskere til det niende Cancer Crosslinks i vår egen Oslo Cancer Cluster Innovasjonspark.

Cancer Crosslinks er den årlige møteplassen for onkologer og hematologer. I 2017 går Cancer Crosslinks av stabelen 26. januar. Vi har delt inn dagen i tre faglige sesjoner som alle presenterer relevante, tverrfaglige temaer med stor klinisk relevans:

• Sesjon 1 “Cancer and Inflammation – new insights and their clinical impact”
• Sesjon 2 “Today’s cancer treatment: how individualized can it be?”
• Sesjon 3 “Classical endpoints vs. Real-world evidence – need to rethink?”

Vi er veldig stolt over å presentere internasjonale toppforelesere fra både Europa og USA som sammen med nasjonale eksperter vil gi innsikt i et fagfelt i rivende utvikling. Åpningssesjonen er med Professor Jerome Galon fra INSERM som blant annet står bak Immunoscore, som er ny metode for rutinemessig klinisk vurdering av prognosen til kreftpasienter. Vi ser også veldig fram til å høre Professor William G. Wierda fra MD Anderson snakke om hvor persontilpasset behandlingen av blodkreft kan gjøres i dag.

Vi håper møtet vil stimulere til tverrfaglig diskusjon og samarbeid “fra laboratorium til sykeseng”.
Presentasjonene vil foregå på engelsk.

Om du har problemer med å registrere deg elektronisk, scann inn svarslippen og send den på mail til jh@oslocancercluster.no. På grunn av stor interesse for Cancer Crosslinks, kan firmaer kun stille med to personer. Kaare Norum Auditorium har plass til 290 deltagere. Møtet vil også bli strømmet direkte.

  • Dersom du trenger fly eller togbillett, ta kontakt med vårt byrå Berg-Hansen på e-mail: bestilling@berg-hansen.no eller på telefonnummer: 08050. Vennligst oppgi kode “OCC”, belastes Oslo Cancer Cluster. Booking vil åpne torsdag 1. desember 2016.

Møtet arrangeres i samarbeid med Bristol-Myers Squibb og AbbVie Norge. Arrangementet er i samsvar med retningslinjene som er inngått mellom Legeforeningen og Legemiddelindustriforeningen. Denne invitasjonen er også sendt til administrasjonen og/eller avdelingsansvarlig, i henhold til sykehusets interne regler.