Introduction to the melanocortin system

Wednesday, February 24th, 2010

The body consists of cells which communicate with each other via signaling molecules to govern and determine a variety of physiological functions in the body. The action and effect of these signaling molecules is mediated by ‘receptors’ which are located on the surface of (plasma membrane), or inside a cell. A molecule that ‘binds’ with a receptor is known as a ligand and can be protein such as a hormone or drug and the role of the ligand is to activate, or inactivate a particular biological activity.

In some ways receptors can be likened to switches with on and off positions, and which in turn affect the cell’s internal functioning. The action or inaction of receptors is determined by the type of ligand with which they bind, i.e. receptors are activated when an agonising ligand, an ‘agonist’ binds and left inactive when an ‘antagonist’ in some way prevents the agonist from binding. The specific biological action is dependent upon which particular ligand binds with a receptor.

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The Clinuvel AGM

Tuesday, November 24th, 2009

melbournetownhallAs many of you may know, this week saw Clinuvel hold its Annual General Meeting in the Melbourne Town Hall. As managing director I welcome these opportunities where I am able to meet and talk to the people whom Clinuvel considers integral to the company and its existence; the Board of Directors sees Clinuvel’s investors as unique. In Clinuvel, an investor has to fundamentally believe in the premise of offering pharmaceutical photoprotection, a novel option, an innovative approach to skin disorders.

In a meeting that would be considered short by international standards I was both excited and proud to present some of the achievements and milestones our team has reached this year, and lay out our plans for the next 12 months.

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Two conferences, one city

Friday, October 2nd, 2009

newyorkThose of you that follow pharmaceutical development and Clinuvel in particular will know that we recently presented at Rodman and Renshaw’s 11th Annual Healthcare Conference in New York. It’s serendipitous that the following week found another conference taking place in the same city, although involving a rather different topic. The coincidence draws attention to a connection that is of increasing urgency and importance.

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The drug development process – Part 3

Tuesday, September 1st, 2009

Test Tubes 1This is a continuation of the post “The drug development process – Part 1” and “The drug development process – Part 2″

The 3 Phases of clinical trials are strictly monitored and controlled by different regulatory bodies such as the FDA (US), the TGA (Australia), the EMEA (EU) and SwissMedic.

All trials must undergo the same rigorous process as outlined in our previous post, but are quite distinctly different and influenced by a number of other factors.

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Administration, formulation and controlling drug release

Friday, August 7th, 2009

The human body functions with an intricately complex system of bioresponse. Put simply, too much of an active substance, as well as too little is undesirable. We have learned to manage and regulate light of various wavelengths over the past ten years with the intention of protecting skin and tissue.

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