Lost Password? No account yet? Register

Advertisement

New Media Advertisement
Glenmark files IND application with US FDA for GBR 500 molecule phase-I trials PDF Print E-mail
User Rating: / 0
PoorBest 
Article Index
Glenmark files IND application with US FDA for GBR 500 molecule phase-I trials
Page 2

Glenmark Pharmaceuticals Ltd. (India) has filed its molecule GBR 500 for phase-I trials with the US FDA.  The filing of this crucial IND (Investigational New Drug Application) signifies the successful completion of a substantial number of pre-clinical studies for its humanized biologic molecule.

GBR 500, a monoclonal antibody, is an antagonist of the VLA-2 (Alpha2 ?eta1) integrin. Since VLA - 2 mediates interaction of cells relevant for the inflammatory process with the extracellular matrix, it has the potential to be a broadly applicable anti-inflammatory compound. Glenmark intends to initially develop GBR 500 for MS (Multiple Sclerosis).

Glenmark expects to complete phase-I trials for GBR 500 in this financial year immediately followed by several proof of concept phase-IIA studies in patients with multiple sclerosis and another common human inflammatory disease. In addition to the essential safety, tolerability and pharmacokinetics testing in phase-I, this study will also evaluate a number of relevant pharmacodynamic inflammatory parameters. These include validated models of inflammatory response in blood and skin, particularly involving T-lymphocytes and neutrophils which are relevant to a number of common inflammatory disorders.

Glenn Saldanha, managing director & CEO, commented, "This is a significant development for the organization. We are excited about the progress made by GBR 500 and glad to have completed all requirements for filing the IND for phase-I trials. The first molecule is always the toughest and it has been a tremendous learning experience for the organization. We would now be able to implement relevant learnings to our other biologic molecule which should hasten the discovery process for biologics in the pre-clinical stage."

Dr Michael Buschle, president-Biologics, Glenmark Switzerland said, "We are excited about the progress we have made with this antibody. We have now a complete preclinical data package at hand to present to the FDA. We are very much looking forward to bringing this molecule into the clinic."

GBR 500, a monoclonal antibody, is a potential first in class compound being initially developed for MS (Multiple Sclerosis). It is an antagonist of the VLA-2 (?2ß1) integrin. VLA-2 mediates interactions of cells with the extracellular matrix. Integrin-mediated cell migration is required for the recruitment of immune cells to sites of inflammation, and Glenmark intends to develop GBR 500 as a modulator of inflammation. The market for MS alone is around USD 7 billion.

Glenmark's other biologic molecule, GBR 600, which is in the pre-clinical stage of development is also a monoclonal antibody directed against a validated key target in the thrombus-forming cascade. GBR 600 is under development at Glenmark's Biologics Research Centre in Switzerland. GBR 600 is being developed for the treatment of acute coronary syndrome and cerebral thrombosis.


 
< Prev   Next >

Retailing

Kmart Pharmacy has launch of the American Fare Dollar Program, which offers pharmacy customers a choice of 10 over-the-counter (OTC) medications from Kmart's proprietary American Fare brand for only…     Readmore

Image

Outsourcing

The pharmaceutical manufacturers in the United States have attacked the proposed pharma policy of India saying that it would contravene the stated goal of liberalizing the sector, and sought some…     Readmore

Image

Homeopathy

The Homeopatic manufacturing units must fulfill the conditions stated by the government of India under 67-G     Readmore

FDA

Invitrogen Corporation, a provider of essential life science technologies for research, production and diagnostics,  has received U.S. Food and Drug Administration (FDA) premarket approval (PMA) for its SPOT-Light(R) HER2…     Readmore

Biotechnology

Attractive incentives and tax soaps offered by the Malaysian government for the biotech and research based companies is luring some major Indian pharmaceutical players to set up units in…     Readmore

Nanotechnology

The UK Royal Commission has issued a report on the spread of nanomaterials, stating that “urgent action [is] needed on testing and regulation”. In its report the Commission found…     Readmore

Packaging

Bilcare Research has launched a product to help check the menace of counterfeit drugs. The product has a label with a unique bar code made out of nanotechnology and…     Readmore