Safety of gpASIT+TM Subcutaneously Administered to Hay Fever Patients With or Without Immunoregulating Adjuvant

Phase 2

Completed

• Conditions: Hay Fever
• Interventions: Biological: gpASIT+TM; Biological: gpASIT+TM + adjuvant

• Registration Number: NCT01506375
• Lead Sponsor: BioTech Tools S.A.

Brief Summary

The aim of the study is to compare the safety, clinical tolerability, immunogenicity and efficacy of gpASIT+TM (grass pollen peptides) alone and combined with an immunoregulating adjuvant, in a short course administration (5 injections over 4 weeks).

Detailed Description

Not available

Study Timeline

• Study Start: 2011-11
• Study First Submitted: 2011-12-07
• Study First Submitted QC: 2012-01-05
• Study First Posted: 2012-01-10
• Status Verified: 2012-08
• Primary Completion: 2013-01
• Study Completion: 2013-04
• Last Update Submitted: 2014-05-23
• Last Update Posted: 2014-05-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

• Subject has given written informed consent

• Age between 18 and 50 years

• The subjects are in good physical and mental health according to his/her medical history, vital signs, and clinical status

• Male or non-pregnant, non-lactating female

• Females unable to bear children must have documentation of such in the CRF (i.e. tubule ligation, hysterectomy, or post-menopausal (defined as a minimum of one year since the last menstrual period))

• Allergy diagnosis:

  • A medical history of moderate to severe seasonal allergic rhinoconjunctivitis (SAR) during the grass pollen season during at least the two previous years
  • A positive skin prick test (wheal diameter ≥ 3 mm) to grass-pollen mixture
  • Specific IgE against grass pollen (IgE > 0.7 kU/l) [using recombinant mixture of rPhl p1 and rPhl p5b Phleum pratense (g213)]

• Subjects never treated by immunotherapy or subjects for whom the immunotherapy ended at December 31, 2009 and who had as well moderate to severe symptoms in the two previous years (2010 and 2011)

Exclusion Criteria

• Subjects with current immunotherapy and subjects who underwent a previous immunotherapy within the last 2 years
• Participation in another clinical trial and/or treatment with an experimental drug within the last 3 months
• A history of hypersensitivity to the excipients of investigational products
• Subjects with perennial asthma (regular intake of inhaled corticosteroids outside the pollen season: consumption on a daily base or patients who are taking a reliever more than twice a week)
• Subjects with severe seasonal asthma requiring long acting beta agonist AND inhaled steroid treatment
• Subjects with a VC < 80% and a FEV1 < 70% of predicted value at the screening visit
• Subjects symptomatic to perennial inhalant allergens who should need antihistamine drug or systemic corticoids to relieve allergic symptoms during the treatment period
• Subjects with documented evidence of chronic sinusitis (as determined by Investigator)
• Subjects with rhinitis medicamentosa, non-specific rhinitis (to food dye, preservative agent...)
• Subjects with a history of renal disease or chronic hepatic disease
• Subject with malignant disease, autoimmune disease
• Any chronic disease, which may impair the subject's ability to participate in the trial
• Subjects requiring beta-blockers medication
• Chronic use of concomitant medications that would affect assessment of the effectiveness of the trial medication (e.g. tricyclic antidepressants)
• Regular consumption of corticoids (oral, topic or nasal) or of anti-histaminic drugs within 4 weeks preceding the trial (screening visit)
• Any consumption of corticoids (oral, topic or nasal) or of anti-histaminic drugs within 1 week preceding the trial (screening visit)
• Subject with febrile illness (> 37.5°C, oral)
• A known positive serology for HIV-1/2, HBV or HCV
• Subjects that are immunocompromised by medication or illness, have received a vaccine, corticoids or immunosuppressive medications within 1 month before trial entry
• Receipt of blood or a blood derivative in the past 6 months preceding trial entry
• Female subjects who are pregnant, lactating, or of child-bearing potential and not protected from pregnancy by a sufficiently reliable method
• Any condition which could be incompatible with protocol understanding and compliance
• Subjects who have forfeited their freedom by administrative or legal award or who are under guardianship
• Unreliable subjects including non-compliant subjects, subjects with known alcoholism or drug abuse or with a history of a serious psychiatric disorder as well as subjects unwilling to give informed consent or to abide by the requirements of the protocol
• Subjects without means of contacting the Investigator rapidly in case of emergency, or not able to be contacted rapidly by the Investigator

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
gpASIT	gpASIT+TM	grass pollen peptides alone
gpASIT/adjuvant	gpASIT+TM + adjuvant	grass pollen peptides + adjuvant

Primary Outcome Measures

Name	Time	Method
Safety of the treatment	up to the end of the grass pollen season	Safety will be evaluated by the following parameters: general physical status, vital signs, haematological parameters, general biochemical parameters, solicited local adverse events, all (serious) adverse events, immunological analysis (total IgG and IgE), inflammatory parameters (CRP) and anti-adjuvant mmunoglobulins.
Clinical tolerability of the treatment	Duration of treatment period (4 weeks)	The clinical tolerability will by assessed through the solicited local adverse events, all (serious) adverse events and the investigator and subject opinion.

Secondary Outcome Measures

Name	Time	Method
Impact of gpASIT+TM with or without adjuvant on the immunological status of the subjects.	up to 1 year after the start of treatment	The following parameters will be assessed: allergen-specific immunoglobulins and blocking antibodies.
Impact of gpASIT+TM with or without adjuvant on the grass pollen allergic symptoms of the subjects.	During the pollen season	The following parameters will be recorded: symptom and rescue medication scores (diary cards), Quality-of-Life (RQLQ(S)).
Long-term follow-up of the patients	1 year after the start of treatment	Safety parameters will be: immunological analysis (Total IgG and IgE), inflammatory parameters (CRP), DnaK-specific immunoglobulins and SAEs.; Immunogenicity parameters will be: evolution of grass pollen specific immunoglobulins and of blocking antibodies.

Trial Locations

Locations (1)

Universitaire Ziekenhuis van Leuven; 🇧🇪 Leuven, Belgium