TFPI Inhibitors – Target Pipeline List

Publisher: La Merie Publishing
Format: Word Table
Product Line:
Target Pipeline List
Product Code: LMTPL032
Release Date: December of 2018

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TFPI Inhibitors – Target Pipeline List

Target: Tissue-factor pathway inhibitor; TFPI; lipoprotein-associated coagulation inhibitor; LACI

This report provides an overview of antibodies targeting TFPI in preclinical or clinical development for treatment of hemophilia with or without inhibitors.

Coagulation factor replacement therapy is still the current standard of care for to the treatment of hemophilia, but its limitations demand novel approaches. Treating haemophilia by restoring thrombin generation may be an effective approach. A promising target for restoring thrombin generation is tissue factor pathway inhibitor (TFPI), a multivalent Kunitz-type serine protease inhibitor that regulates tissue factor-induced coagulation via factor Xa-dependent feedback inhibition of the tissue factor-factor VIIa complex.

Inhibition of TFPI reverts the coagulation process to a more primitive state evolutionarily, whilst regulation by other natural inhibitors is preserved. As well as improving thrombin generation in the range associated with mild haemophilia, anti-TFPI therapies have the advantage of subcutaneous administration. Clinical trials with anti-TFPI antibodies have shown first clinical proof-of-concept and evaluation is ongoing with various molecules in preclinical and clinical stages.

La Merie Publishing offers a low-cost product service providing information about active R&D projects for a given target in the format of Word tables.

The Word document with the Table is delivered by e-mail within 24 hours after receipt of the confirmed order. Usually, delivery time is less than one hour if ordered during European business hours.

The Target Pipeline List in the Word table contains information about:

File: ID no. in proprietary database
Drug name: trade name, INN, drug code(s), trivial name
Target/MoA: mechanism of action
Class of compound: description of type of molecule, formulation, way and mode of administration, application device
Company: originator of molecule and licensee(s) with territories
Category: treatment modalities, i.e. antibody, protein, peptide, RNA, DNA, cells, vaccine, small molecule
Indication: medical indication evaluated in preclinical or clinical study, combination regimens
R&D Phase: from research to market with reference to indication/study
Message: last verified information about project with source and date of information and hyperlink leading to source of information

Research methodology:
Information about R&D projects is identified and retrieved from company publications including, but not limited to, press releases, presentations, website disclosures, SEC publications, regulatory documents, scientific abstracts and full papers, patent applications. Furthermore, public and proprietary databases are used including national and regional clinical trial databases, PubMed.

 


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This Report is NOT a downloadable item but will be delivered via email within 24 h (working days only).

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