Food Allergy to Fish Clinical Trial
Official title:
A Multinational Phase IIb Study to Investigate the Efficacy and Safety of Subcutaneous Immunotherapy With a Modified Fish- Parvalbumin Given in Single Rising and Maintenance Doses to Subjects Allergic to Fish
This is a phase IIb clinical trial to investigate the efficacy and safety of subcutaneous immunotherapy with a modified parvalbumin called mCyp c 1 for the treatment of fish allergy to subjects allergic to fish.
Fish allergy is a persistent food allergy (usually lifelong) which can be life threatening
due to the danger for anaphylaxis (severe allergic reaction) upon accidental exposure to
fish. Until today there is no curative treatment for fish allergy. The only treatment is
avoidance. Patients with fish allergy have to avoid fish of all types and carry an
adrenaline autoinjector and rescue medication, in case of accidental exposure to fish. That
way patients with fish allergy have to continuously control what they are eating and this
causes a great deal of stress and impacts their quality of life.
The major allergen responsible for fish allergy is the protein parvalbumin. It is recognized
by the vast majority (96-100%) of fish allergic patients.
During the past, treatment of food allergy with immunotherapy was successful but dangerous,
due to serious side effects (anaphylaxis).
A novel biotechnological product, a recombinant hypoallergenic parvalbumin, called mCyp c 1,
is used for the first time in a phase IIb clinical trial, to test the efficacy of
subcutaneous immunotherapy for the treatment of fish allergy. The investigational medicinal
product mCyp c1, is based on the recombinant wild type carp parvalbumin (rCyp c 1) and is
the result of site directed mutagenesis, by which the disruption of the two calcium binding
sites of carp parvalbumin is performed. The modified parvalbumin mCyp c 1, is both
hypoallergenic and immunogenic. That way it is a promising molecule for the safe and
effective treatment of fish allergy.
This molecule has proven to be safe in a phase I/IIa study that has been performed, during
which mCyp c 1 was administered with subcutaneous injections. During this study only local
reactions at the injection site were observed. There were no observed systemic reactions.
Even more, there were clear indications that mCyp c 1 was recognized by the immune system.
The results of this phase I/IIa study guarantee the necessity of a phase IIb clinical trial
with mCyp c 1, in order to study the efficacy of this modified parvalbumin in the treatment
of fish allergy.
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