doses, and treatment
regimens. Each of the currently ongoing and planned studies is
aimed at gaining wider experience for this novel treatment approach
and to bring us closer towards a causal and disease-modifying
therapy for a broad range of allergic diseases."
Cytos Biotechnology will host a conference call and
Q&A session today, Tuesday, March 13, 2007 at 9.30 am CET to
discuss the study findings.
To access the conference call, please dial the
following numbers:
Europe +41 91 610 56 00
U.S. +1 866 291 41 66
U.K. +44 207 107 06 11
The conference call will be held in English and
will also be accessible by webcast on the internet. You may follow
the call live or have it replayed later on demand. To access the
webcast and the presentation, please follow the link provided on
our homepage www.cytos.com. The presentation slides will be
available for download 30 minutes prior to the conference call.
About the phase IIa study and the analysis
The randomized, double-blind and placebo-controlled phase IIa study
included 40 male and female patients aged 18 to 65 and suffering
from mild to moderate seasonal allergic rhinitis due to grass
pollen allergy. Upon entry into the study, the allergic status of
the individual participants was recorded by the conjunctival
provocation test, a commonly used allergy test. The study
participants were randomized into 4 treatment groups with 10
patients each and received 6 weekly injections of either i) 300 ?g
CYT003-QbG10, ii) 300 ?g CYT003-QbG10 plus Alum, iii) placebo (PBS
or Alum), or iv) 300 ?g CYT003-QbG10 plus grass pollen extract
(this last group was handled exploratory and open-label). Two weeks
after the last dose, the allergic status of the patients was again
assessed by the conjunctival provocation test. All 40 patients were
included into the analysis.
Ab
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