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Curtana

Patented small molecule therapeutics that target cancer stem cells for the treatment of glioblastoma and other brain cancers

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 Curtana project word cloud

Explore the words cloud of the Curtana project. It provides you a very rough idea of what is the project "Curtana" about.

instrumental    indicate    feasibility    over    care    inhibiting    accounting    tumours    little    cancers    relative    drive    expansion    small    patients    cure    primary    rates    crosses    centre    expressed    deadliest    reduce    standard    bioavailable    malignant    14    found    therapies    investors    potent    ovarian    olig2    most    drugs    ct    killing    drug    rate    68       index    survival    people    80    median    worldwide    cytotoxic    orally    lung    curtana    answer    nervous    13    clinical    bulk    improvement    treatment    radiosensitiser    tolerated    179    gliomas    killer    cancer    identification    compound    blood    die    transcription    molecule    diagnosed    central    kills    biggest    conventional    approval    diagnoses    endometrial    trials    tumour    ineffective    offers    therapeutic    glioblastoma    stem    tumorigenesis    brain    benefit    marketing    aggressive    too    cells    255    months    45    barrier    hope    progression   

Project "Curtana" data sheet

The following table provides information about the project.

Coordinator
CURTANA PHARMA LTD 

Organization address
address: 72 GREAT SUFFOLK STREET
city: LONDON
postcode: SE1 0BL
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website http://www.curtanapharma.com/
 Total cost 71˙429 €
 EC max contribution 50˙000 € (70%)
 Programme 1. H2020-EU.3.1.3. (Treating and managing disease)
 Code Call H2020-SMEINST-1-2016-2017
 Funding Scheme SME-1
 Starting year 2017
 Duration (year-month-day) from 2017-02-01   to  2017-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CURTANA PHARMA LTD UK (LONDON) coordinator 50˙000.00

Map

 Project objective

Over 45,000 people die each year in Europe – and 255,000 worldwide – from cancers of the brain and central nervous system. Gliomas are the biggest killer, accounting for a third of all diagnoses and 80% of primary malignant brain tumours. Among these glioblastoma is the most common, most aggressive and deadliest. Standard of care treatment offers little hope for patients diagnosed with gliomas: there is no cure, the median survival is 14.6 months and the 2-year survival rate is 13.5%. Conventional therapies can reduce tumour bulk, but they are ineffective at killing the cancer stem cells that drive tumour progression. Curtana may have found the answer. Its novel approach targets a transcription factor, Olig2, which is instrumental in tumorigenesis, tumour expansion and survival. By inhibiting Olig2, Curtana’s small molecule compound, CT-179, kills cancer stem cells. Pre-clinical results show CT-179 to be cytotoxic in selected tumours, a potent radiosensitiser, orally bioavailable and well tolerated; it also crosses the blood-brain barrier and has a high therapeutic index relative to conventional cancer drugs. Most importantly, it increases survival rates (in early studies, median improvement was 68%). Results indicate it may have benefit for other cancers too – any in which Olig2 is highly expressed, including all gliomas and other cancers such as lung, ovarian and endometrial. The Phase 1 project will address the feasibility of carrying out the further pre-clinical and clinical studies required before Curtana can apply for drug marketing approval. This will include identification of clinical partners for multi-centre trials that would be carried out in Europe in Phase 2, as well as potential investors.

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The information about "CURTANA" are provided by the European Opendata Portal: CORDIS opendata.

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