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Virobay and LEO Pharma Initiate a Phase 1 Trial of VBY-891, a Compound Intended for Oral Treatment of Psoriasis
Publish date: Mar 18, 2013
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PR Newswire MENLO PARK, California and BALLERUP, Denmark, March 18, 2013
MENLO PARK, California and BALLERUP, Denmark, March
18, 2013 /PRNewswire/ -- Virobay, Inc. and LEO Pharma A/S today announced that their collaboration on the development of an oral treatment for psoriasis
has reached an important milestone as Virobay has now initiated a Phase 1 clinical trial of VBY-891 - a selective cathepsin
S inhibitor. (Logo: http://photos.prnewswire.com/prnh/20130221/595427
) The first Phase 1 trial of VBY-891 is a double-blind, randomized, placebo-controlled study designed to evaluate the safety,
tolerability, pharmacokinetics and pharmacodynamics of single and multiple escalating doses of VBY-891 in healthy adults. "The initiation of this Phase 1 trial represents a significant development objective for Virobay's collaboration with LEO
Pharma," stated Robert Booth, Ph.D., Chief Executive Officer of Virobay. "Virobay has plans
to initiate clinical studies with additional cathepsin inhibitors during 2013 as we seek to develop new therapies for underserved
diseases. Published prelinical data suggest that cathepsin S inhibition may provide a therapeutic benefit in patients with
dermatological disorders such as psoriasis. In addition, our own preclinical data with selective cathepsin S inhibitors has
demonstrated efficacy in models of both psoriasis and atopic dermatitis," stated Robert Booth.
"We look forward to assessing the data from these Phase 1 trials, which will incorporate the evaluation of several biomarkers,
to guide our Phase 2 clinical development plans for VBY-891." "Reaching this important milestone in our collaboration with Virobay brings us one step closer to provide an oral treatment
for psoriasis patients. We believe that VBY-891 has the potential to provide an oral treatment that may alleviate symptoms
of psoriasis. LEO Pharma strives to constantly expand and improve treatment options for patients and this is an important
example of our commitment to meeting patient needs. To the best of our knowledge, the VBY-891 compound has the potential to
be the first in class on the market," said Kim Kjøller, Senior Vice President, Global Development, LEO Pharma. Background About Cathepsin S and VBY-891 Cathepsin S is a member of the cysteine protease family of cathepsin inhibitors that catalyzes the final proteolytic step
in the processing of invariant chain in specific antigen presenting cells. This step is essential in the maturation and loading
of MHC Class II with antigenic peptides and subsequent activation of CD4+ T cells. Continuous presentation of antigenic self-peptides
is thought to be involved in the maintenance of chronic disease in autoimmune disorders, including psoriasis. Inhibition of
cathepsin S is likely to result in a reduction in antigen presentation without an impact on innate immunity. VBY-891 is a next generation cathepsin S inhibitor that is a potent, competitive and reversible inhibitor of purified cathepsin
S. It has picomolar inhibitory potency against the cathepsin S enzyme and nanomolar inhibitory potency in cellular assays.
VBY-891 is also highly selective against human cathepsins L, B, F and K. Sustained cathepsin S inhibition after oral
dosing has been demonstrated in vivo through the use of a biomarker. VBY-891 shows potent inhibitory activity in models
of autoimmunity and neuropathic pain. Therefore, inhibition of cathepsin S may have therapeutic potential across a range of
dermatological conditions. About the collaboration The multi-million dollar collaboration between Virobay Inc. and LEO Pharma A/S was entered in 2012 when LEO Pharma in-licensed
the promising compound from Virobay. The collaboration agreement involves up-front payment to Virobay of USD
7m, followed by milestone payments totalling up to USD 300m and tiered to royalties.
The compound has been tested in pre-clinical studies and the project is now entering the next phase - a phase 1 clinical trial
in healthy human volunteers. After this trial has been completed, the plan is to do testing on psoriasis patients later this
year. If the process proceeds as planned, the collaboration may result in an oral treatment for psoriasis in 6-7 years. About Virobay, Inc. Founded in 2006, Virobay is a leader in the design, synthesis and development of small molecule inhibitors of cysteine
proteases, a class of enzymes that are key mediators in a variety of diseases, including autoimmunity, neuropathic pain, liver
disease, cancer and cardiovascular disorders. Virobay's clinical pipeline currently includes product candidates in autoimmune
disease, neuropathic pain and liver fibrosis. For more information, please visit http://www.virobayinc.com
About LEO Pharma LEO Pharma helps people achieve healthy skin. By offering care solutions to patients in more than 100 countries globally,
LEO Pharma supports people in managing their skin conditions. Founded in 1908 and owned by the LEO Foundation, the healthcare
company has devoted decades of research and development to delivering products and solutions to people with skin conditions.
LEO Pharma is headquartered in Denmark and employs approximately 5,000 people worldwide. For more information, visit http://www.leo-pharma.com. SOURCE Virobay, Inc. and LEO Pharma A/S
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