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BLMs 4 TB SIGNED

Beta-lactams for Tuberculosis Treatment

Total Cost €

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EC-Contrib. €

0

Partnership

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 BLMs 4 TB project word cloud

Explore the words cloud of the BLMs 4 TB project. It provides you a very rough idea of what is the project "BLMs 4 TB" about.

clinical    renewed    infections    deadly    glaxosmithkline    gsk    last    arose    treatments    barros    microscopy    track    mathematical    transcriptomic    iacute    longer    pharmacokinetic    questions    24    techniques    trial    ram    resistance    head    life    first    treatment    modeling    patients    pursued    trials    anti    subset    outcome    bacterial    poor    antibiotics    disease    decades    generation    lactams    adherence    pk    urgently    report    cephalosporins    resistant    combo    point    mdr    agents    garc    quality    leads    carbapenem    carbapenems    drug    optimal    unclear    prevent    proteomic    time    inform    oacute    xdr    dosage    unpleasant    therapies    months    extensively    answer    led    tb    family    meropenem    specificities    dr    linked    undergo    killing    safest    never    50    positive    iia    pd    therapy    administration    market    microbiology    dim    infectious    molecular    validated    frequency    severe    strains    treat    relapse    data    lapse    takes    beneficiary    outcomes    cephems    ineffective    blm    pharmacodynamics    prospects    hope    infected    record    regarded    beta    shorten    tuberculosis    worldwide    blms    virtually    discontinued   

Project "BLMs 4 TB" data sheet

The following table provides information about the project.

Coordinator
FUNDACION AGENCIA ARAGONESA PARA LA INVESTIGACION Y EL DESARROLLO 

Organization address
address: PASEO MARIA AGUSTIN 36 EDIFICIO PIGNATELLI PTA 30 PL 2
city: ZARAGOZA
postcode: 50004
website: www.araid.es

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 Spain [ES]
 Total cost 170˙121 €
 EC max contribution 170˙121 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-SE
 Starting year 2018
 Duration (year-month-day) from 2018-04-01   to  2020-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACION AGENCIA ARAGONESA PARA LA INVESTIGACION Y EL DESARROLLO ES (ZARAGOZA) coordinator 170˙121.00

Map

 Project objective

Tuberculosis (TB) is the most deadly infectious disease worldwide. TB therapy takes 6 months with unpleasant side effects that leads to poor adherence and the development of drug resistance. Patients infected with multi (MDR) or extensively (XDR) drug resistant strains must undergo longer treatments (up to 24 months) associated with even severe side effects and only 30-50% positive treatment outcomes. New treatments are urgently needed.

Beta-lactams (BLMs) are the safest antibiotics in the market with a long track record of clinical use to treat bacterial infections. They were, however, traditionally regarded as ineffective for TB therapy to the point that research was virtually discontinued for the last three decades. A renewed interest recently arose after a report of Phase IIa clinical trial validated the potential of meropenem (a carbapenem). This study was led by Dr. Barros, Head TB unit GlaxoSmithKline (GSK) (the beneficiary of this proposal). In addition, Dr. Ramón-García (the applicant) just identified first-generation cephalosporins (cephems), a subset of the BLM family never pursued for TB therapy, as potential anti-TB agents. Promoting BLM development is the best immediate hope for TB patients that currently have very dim life prospects.

Carbapenems and cephems have different anti-bacterial killing properties, pharmacokinetic (PK) and pharmacodynamics (PD) parameters. These specificities affect therapy design for an optimal clinical outcome. Although promising, it is still unclear how BLMs should be included in new combo therapies (i.e. dosage, duration and frequency of administration) to shorten the duration of TB therapy, prevent relapse and treat M(X)DR-TB.

To answer these questions, I will use time-lapse microscopy linked to mathematical PK/PD modeling, transcriptomic and proteomic studies and clinical microbiology techniques to provide high quality molecular and PK/PD pre-clinical data to inform the design of future BLM TB clinical trials.

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The information about "BLMS 4 TB" are provided by the European Opendata Portal: CORDIS opendata.

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