Curalogic is ready to commence a clinical study with the house dust mite product


Announcement no. 24/2007                                                        


To the OMX Nordic Exchange	                           Copenhagen, November 29,  
2007                                                                            






Curalogic is ready to commence a clinical study with the house dust mite product
                                                                                

Summary: Curalogic has received all necessary permissions to start a Phase II   
clinical study (DME 01) with the product for the treatment of house dust mite   
allergy. The market for Curalogic's house dust mite product is large as about 52
million people in Europe and 30 million people in the United States suffer from 
house dust mite allergy.                                                        
                                                                                
Curalogic has obtained permission from the German regulatory authorities (the   
Paul Ehrlich Institute) and the “Landesamt für Gesundheit und Soziales Berlin”  
(the ethical committee of Berlin) to start a Phase II clinical study (DME 01)   
with the product for the treatment of house dust mite allergy.                  
                                                                                
The study objective is to test the tolerability of escalating doses of orally   
administered house dust mite extract to patients suffering from house dust mite 
allergy. According to the plan, 30 patients will participate in the study, which
will be conducted at a single clinical centre in Berlin, Germany. It is expected
that the first patients will be dosed before Christmas 2007, and the results    
from the study are scheduled to be published in the third quarter of 2008.      

Design of the clinical study                                                    
DME 01 is a double-blinded, randomized, placebo-controlled study, with the      
primary objective to                                                            
determine the maximum tolerated dose, i.e. the highest dose that can be         
administered without too many side effects. A secondary objective will be to    
evaluate the safety of the house dust mite product. Patients with moderate to   
severe house dust mite allergy will be treated daily with escalating doses of   
house dust mite extract. The dose level will be increased every week after a    
thorough safety evaluation at the previous dose level.                          

Curalogic's product for the treatment of house dust mite allergy                
The program targets registration both in the United States and Europe. The two  
most predominant house dust mite species in the United States and Europe are D. 
pteronyssinus and D. farinae. The active ingredients in the product for treating
allergy to house dust mites will therefore comprise a mixture of extracts of    
these two species of house dust mites.                                          

House dust mite allergy                                                         
About 52 million people in Europe and 30 million people in the United States    
suffer from house dust mite allergy. Patients suffering from allergy to house   
dust mites have allergy symptoms year round.                                    


Yours Sincerely,                                                                

Curalogic A/S                                                                   


For additional information, please contact:                                     
Peter Moldt, President and CEO, 	Phone +45 99 99 24 00, mobile +45 26 25 04 22  
Helle Busck Fensvig, EVP and CFO, 	Phone +45 99 99 24 00, mobile +45 20 70 55 37


About Curalogic                                                                 
Curalogic is a Danish biopharmaceutical company listed on the OMX Nordic        
Exchange (CUR.CO) as a small cap + company. Curalogic develops innovative       
products for the treatment of allergy using a patented formulation technology.  
The products combine the efficacy of immunotherapy with the patient friendliness
of antihistamines and have the potential to become the preferred type of allergy
treatment among patients. Curalogic has a broad and mature pipeline of products 
for the treatment of ragweed allergy and grass allergy in Phase III, and        
products for the treatment of house dust mite allergy and cat allergy in Phase  
II.                                                                             













































This announcement contains forward-looking statements regarding the Company's   
future financial development and performance and other statements which are not 
historical facts. Such statements are made on the basis of assumptions and      
expectations which, to the best of the Company's knowledge and belief, are      
reasonable, at this time, but may prove to be erroneous in the future.

Anhänge

announcement_about_permission_to_start_dme_01.pdf