MUMBAI, August 10, 2011 /PRNewswire/ --
- Revamilast is a PDE4 inhibitor, under development for Asthma, Rheumatoid Arthritis and other inflammatory disorders
- The molecule successfully completed pre-clinical trials and Phase I studies
- Phase I studies on healthy volunteers were carried out mainly in the UK
- Glenmark has initiated global Phase IIb studies for both indications in Europe and Asia
- Huge unmet medical need as globally they are over 300 million Asthma patients and over 20 million Rheumatoid Arthritis patients
Glenmark Pharmaceuticals today announced that its Novel Chemical Entity "Revamilast" (GRC 4039) has initiated Phase IIb human dose range finding trials globally. Revamilast is an orally active, potent and selective inhibitor of phosphodiesterase 4 (PDE 4) that is currently being developed by Glenmark for the treatment of chronic inflammatory disorders such as Asthma, Rheumatoid Arthritis (RA) and other inflammatory diseases. The Phase IIb studies that will be carried out will help establish the efficacy and safety of the molecule and will also provide dose range finding data for Revamilast.
Dr. Steffen Stuerzebecher, President & Chief Medical Officer, Glenmark Pharmaceuticals Ltd said "The clinical trials and the animal studies data for Revamilast are promising for both indications i.e. Asthma and Rheumatoid Arthritis. There is a huge unmet need for both these chronic medical conditions globally. For Glenmark, this is a significant development as we have built on more than a decade of experience in the PDE 4 space to progress an exciting molecule to Phase II human trials."
In Phase I studies carried out mainly in the United Kingdom, nearly 150 healthy volunteers have been dosed and no Serious Adverse Events have been noted. The pharmacodynamic evaluation in healthy human volunteers treated with Revamilast suggests a good ex-vivo inhibition of the inflammatory marker TNF- with maximum inhibition upto 93%. Based on these results and animal model data, it is expected that Revamilast would be beneficial in a variety of inflammatory disorders. Additionally, Revamilast does not appear to be metabolized to carcinogenic metabolites (ADCP N-oxide and ADCP N-oxide epoxide); and plasma samples from a Phase 1 study analyzed for such metabolites of Revamilast, showed no levels were detected in human plasma.
With the completion of several Phase I studies, Glenmark has initiated a global Phase IIb trial for Revamilast in patients with Asthma. Glenmark has already received approval from respective authorities in the UK, Poland, India and Czech Republic to conduct Phase IIb studies. Regulatory submissions have also been completed in Russia. The primary objective of this 12-week, double blind, placebo controlled, dose range finding study is to evaluate the effects of Revamilast at three doses on lung function (FEV1) in nearly 450 patients with chronic persistent Asthma.
Glenmark has also initiated another global Phase IIb trial with Revamilast in patients with Rheumatoid Arthritis. Glenmark has already received approval from the MHRA, UK, India, Poland and the Philippines to conduct Phase IIb studies for Rheumatoid Arthritis. Regulatory submissions have also been completed in Sri Lanka. The objective is to determine the efficacy of three doses of Revamilast compared to placebo in the treatment of more than 400 patients with active Rheumatoid Arthritis who showed an inadequate response to methotrexate.
In parallel to these two clinical studies, Glenmark is also conducting various other clinical and non-clinical studies to ensure timely entry into Phase III trials. Glenmark intends to initiate Phase III trials for at least one indication in the second half of FY 2012-13
PDE4 inhibitors (Impact on Asthma and RA)
PDE 4 inhibitors represent class of therapeutic agents with a unique mechanism of action for the treatment of a range of chronic inflammatory disorders including COPD, asthma, rheumatoid arthritis, IBD and psoriasis. This mechanism of action of PDE4 inhibitors would be useful in treating chronic inflammatory conditions such as RA and asthma. Many manifestations of RA are significantly influenced by the effects of pro-inflammatory cytokines (e.g., TNF, IL-1, IL-6). In asthma, there remains a need for the development of novel anti-inflammatory therapies that are at least equally effective and possess a superior safety profile in comparison to corticosteroids.
PDE 4 inhibitors relax smooth muscles and attenuate the inflammatory response to a wide variety of stimuli and in particular suppress many cytokines, including TNF- production in mononuclear cells. Therefore, PDE 4 inhibitors present a novel treatment opportunity for a range of chronic inflammatory diseases.
A first-in-class PDE 4 inhibitor, Roflumilast, has recently been approved in the European Union and in Mar'2011, Forest Laboratories Inc. and Nycomed A/S have received US FDA approval for Roflumilast to treat symptoms associated with severe chronic obstructive pulmonary disease (COPD).
Globally there are over 300 million asthma patients and over 20 million patients have RA. The current RA market is estimated at USD 26 billion and the Asthma market is estimated at USD 30 bn
About Glenmark Pharmaceuticals Ltd
Glenmark Pharmaceuticals Ltd. (GPL) is a research-driven, global, integrated pharmaceutical company headquartered at Mumbai, India. It is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity). Glenmark has eight molecules in various stages of clinical development and is primarily focused in the areas of Inflammation [asthma/COPD, rheumatoid arthritis etc.] Pain [neuropathic pain and inflammatory pain] and Oncology[Luekemias/Lymphomas]. The company has a significant presence in branded generics markets across emerging economies including India. GPL along with its subsidiary has twelve manufacturing facilities in four countries and has five R&D centres.
For further information, please contact:
Glenmark, Mumbai, India Tel: [+91-22]40189919
Email : email@example.com
SOURCE Glenmark Pharmaceuticals Ltd.