has decided to embark on the path of fine-tuning and developing rhNGF in its formulation for clinical use, at its own biotech facility in L’Aquila. and in Naples, where there are the laboratories of Drug Discovery and Technology Formulation, within a long-term collaboration with CNR. Italian excellence: the Dompé Hub in L’Aquila. Dompé has concentrated its manufacturing and research and development activities at its L’Aquila hub.

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Home Research and Innovation Our research. At this point we move on to formu,ation second phase of packaging in boxes, wrapping and pallets. This site uses third party cookies. You are going to leave this site.

Therefore these two amino acid changes have no influence on the final active ingredient rhNGFwhich is identical to the naturally secreted human protein.

Our research

We suggest you to update it for free by following one of the these links, choosing the browser you prefer: For information, including how to forrmulation the cookies, click here.

Radhakrishnan and Dr B.

Do you want to be redirected to the mobile version? There are seven packaging lines in total for synthetic pharmaceutical products: The pro-sequence is further cleaved during the production process by enzymatic hydrolysis.

In the downstream process the proNGF is first checked for its correct three-dimensional structure folding phase and then purified.

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Informultaion drug designations in the E. DrugsOrganic ChemistryFda. Reparixin is the first of a new class of low-molecular-weight inhibitors that is selectively capable of modulating the activity of the receptor through an allosteric mechanism of action. Click here to learn more.

LAquila hub | Dompé

By continuing to use this web site, you are consenting to the use of cookies. In the turnover was million is focused both on the development of pharmaceuticals for formulatiin needs as yet unfulfilled, in the areas of ophthalmology, oncology, diabetes and organ transplant, as well as in the creation of innovative industrialisation processes of these.

The intervention concerned the creation of new areasconsisting of a four-storey building dedicated to the production process of coated granules, a three-storey building for packaging and a new warehouse.

The production process for granules includes an initial phase of dispensing weighing of the raw materials active ingredient and excipients. The areas of activity are: Cenegermin August 23, 9: Join 2, other followers. From Italy to the world: Primary packaging — in a controlled air environment — in which the pharmaceutical product is inserted into the individual stick, packet formulwtion container.

Regarded as among dompr world’s foremost experts on corneal diseases, he was appointed Adjunct Assistant Professor of Biology at Temple University of Philadelphia. Do you want to be redirected to the mobile version?

L’Aquila hub

The chemokine CXCL8 plays a key role in the recruitment and activation of dkmpe neutrophils in post-ischemia reperfusion injury after organ transplantion. Dlmpe suggest you to update it for free by following one of the these links, choosing the browser you prefer: In the first study, only patients with the disease in one eye were enrolled, while in the second study, patients with the disease in both eyes were treated in both eyes bilaterally.

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He has earned a PhD in the research of the regenerative role of NGF in ocular degenerative syndromes. Provide answers to unresolved health-related questions in order to meet the needs of patients worldwide.

Our research | Dompé

Clinical studies are dpmpe developed in cooperation with the above counterparts to ensure the highest level of safety to their participants, operating dome full compliance with the scientific and ethical standards that govern clinical research and sharing the results of the research conducted with the scientific community, regulatory authorities and institutions. Another noteworthy activity concerns the joint participation of programmes of international research, such as those related to the Horizon call.

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The facility thus has the capacity to develop, transfer and validate most of the analytical methods needed for issuing GMPs and characterising biomolecules.