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BLMs 4 TB SIGNED

Beta-lactams for Tuberculosis Treatment

Total Cost €

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EC-Contrib. €

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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.

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

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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