Follow Us

ImMucin cancer vaccine reaches final clinical trials

If vaccine passes 'Phase III' trials, ImMucin may be only six years from widespread distribution

The ImMucin cancer vaccine has just entered "Phase III" clinical trials at Jerusalem's Hadassah University Medical Center. If the vaccine passes this phase, the drug will go to the appropriate regulatory authorities in countries around the world. After passing regulatory review, the drug would be able to enter the drug market about six years from now.

The ImMucin vaccine is produced by Vaxil BioTherapeutics, a clinical-stage company (so called because all of its products are in the early stages of development and testing; not yet ready for the market). Vaxil develops therapeutic and preventive vaccines for cancer and tuberculosis. ImMusin is synthetically derived from the MUC1 protein, which is associated with more than 90% of solid tumour cancers and a number of non-solid tumours.

ImMucin works by stimulating the patient's immune system to selectively target tumour cells. According to Vaxil, ImMucin does not contain any "non-specific" epitopes (an epitope is a the part of a antigen or foreign molecule that causes the body to produce antibodies), that allow the immune system to target just tumour cells instead of attacking other non-cancerous parts of the body that also contain the MUC1 protein. Vaxil saysu that the preclinical studies have shown ImMucin to induce a stronger immunity against MUC1 compared with other MUC1-derived derived vaccines.

ImMucin has the unique ability to tell the body which cells to attack. Julian Levy, the CEO of Vaxil, told United With Israel, "the body knows something is not quite right but the immune system doesn't know how to protect itself against the tumour like it does against an infection or virus. This is because cancer cells are the body's own cells gone wrong." In other words, ImMucin is intended to enhance the immune system so that it can track down and destroy the cancer.

ImMucin will be tested on a large number of patients (hundreds to thousands of individuals) in the Phase III trials. Once the drug has proved successful and passes each country's regulations, it may then go on the market in that country. After it reaches the market, there are two more phases to evaluate the long-term effects on patients and to further integrated it into widespread public treatment.






Send to a friend

Email this article to a friend or colleague:

PLEASE NOTE: Your name is used only to let the recipient know who sent the story, and in case of transmission error. Both your name and the recipient's name and address will not be used for any other purpose.

Techworld White Papers

Desktop modernisation

On the one hand, there is the need to keep the existing desktop environment efficient, secure...

Download Whitepaper

Top 10 myths about virtualising business-critical applications

Even though virtualization has brought positive change to enterprise IT over the last decade,...

Download Whitepaper

Aligning CFO and CIO priorities

Forward-thinking organisations are viewing cloud computing as an investment in business...

Download Whitepaper

The new corporate network

Businesses can’t afford to have employee productivity suffer because they cannot use their...

Download Whitepaper

Techworld UK - Technology - Business

Techworld Mobile Site

Access Techworld's content on the move

Get the latest news, product reviews and downloads on your mobile device with Techworld's mobile site.

Find out more...
LogMeIn Rescue

Accelerate Your IT Efficiency

View the latest capacity management resources including whitepapers, videos and news.

Find out more...

Site Map

* *