Phase II Trial With Subcutaneous Immunotherapy in Patients Sensitized to Phleum Pratense

Phase 2

Completed

• Conditions: Allergic Rhinoconjunctivitis
• Interventions: Biological: Allergovac Depot; Biological: Placebo

• Registration Number: NCT01567306
• Lead Sponsor: Roxall Medicina España S.A

Brief Summary

Based on EMA (European Medicines Agency) new guidelines on the clinical development of products for immunotherapy for the treatment of allergic diseases the aim of this study is to establish a dose-response relationship for clinical efficacy of Phleum pratense pollen extract subcutaneous vaccine.

Detailed Description

In adherence to EMA guidelines, the Phase I Clinical trial was carried out using Phleum pratense extract in depot presentation using 3 different dose escalation scheme. The objective was to compare tolerance and safety of the three dose escalation scheme as well as to determine the maximum dose tolerated by the population.

Once the range of tolerated doses was established, and following the strict norms of the EMA, a Phase II dose response clinical trial was designed wherein the efficacy of subcutaneous immunotherapy in depot presentation could be compared in 5 different doses. One of these doses will be the MTD established by the population in the first study, another will be lower than this dose, and three will be greater than it. The dose escalation scheme to be tested was chosen based on the results of the aforementioned clinical trial. As dictated by EMA norms, a control placebo will be used.

Study Timeline

• Study Start: 2011-10
• Study First Submitted: 2012-03-23
• Study First Submitted QC: 2012-03-29
• Study First Posted: 2012-03-30
• Primary Completion: 2013-04
• Study Completion: 2013-04
• Results First Submitted: 2018-08-09
• Status Verified: 2019-01
• Results First Submitted QC: 2019-01-28
• Last Update Submitted: 2019-01-28
• Results First Posted: 2019-04-29
• Last Update Posted: 2019-04-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 151

Inclusion Criteria

1. Patients must sign the Informed Consent Form.

2. Patients must be between 18 and 60 years of age.

3. Patients with seasonal allergic rhinoconjunctivitis produced by Phleum pratense during at least 2 years prior to participating in the study. Although the pathology being studied is allergic rhinoconjunctivitis, patients who have concomitant mild or moderate asthma may be included.

4. Patients who have had a skin prick test result equal or more than 3 mm in diameter against Phleum pratense.

5. Patients who have specific IgE equal or more than class 2 (CAP/PHADIA) to Phleum pratense.

6. Patients will preferably be monosensitized to Phleum pratense. Polysensitized patients may only be included in the study if their other sensitizations are produced by:

   • Overlapping seasonal pollens which are cross-reactive with Phleum pratense.
   • Pollens whose seasons do not overlap with Phleum pratense and which are not expected to produce symptoms during the study period.
   • Other allergens which are not expected to produce symptoms during the study period.

7. Women of child-bearing potential must have a negative urine pregnancy test at the time they begin the study.

8. Furthermore, women of child-bearing potential must agree to use adequate contraceptive methods during this study if they are sexually active.

Exclusion Criteria

1. Patients with stable and continued use of allergy medication during the 2 weeks prior to their inclusion in the study.
2. Patients sensitized to allergens with overlapping seasons but which are not cross-reactive with Phleum pratense and with specific IgE levels equal or less than class 2 CAP/PHADIA.
3. Patients who have received immunotherapy in the 5 years prior to the study against either the allergen being tested or an allergen which is cross-reactive, or who are currently receiving immunotherapy for any other allergen.
4. Patients with severe asthma or FEV1 < 70% or with asthma which requires treatment with inhaled or systemic corticoids at the time of the study or in the 8 weeks immediately prior to the onset of treatment.
5. Patients with immunological, cardiac, renal or hepatic diseases or any with any other illness which the investigators deem may interfere with the study.
6. Patients with a prior history of anaphylaxis.
7. Patients with chronic urticaria.
8. Patients with moderate-severe atopic dermatitis.
9. Patients with clinically relevant malformations of the upper respiratory tract.
10. Patients who have participated in another clinical trial within 3 months prior to this study.
11. Patients being treated with tricyclic antidepressants, psychotropic drugs, beta-blockers, or angiotensin-converting enzyme inhibitors (ACEIs).
12. Women who are pregnant or breast-feeding or are of child-bearing age and who do not agree to use adequate contraception if they are sexually active and who have not demonstrated that they have been surgically sterilized or have other means of not bearing children.
13. Patients who cannot attend study visits.
14. Patients who are uncooperative or refuse to participate in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Allergovac Depot Group 1 Active	Allergovac Depot	-
Placebo - Group 6	Placebo	-
Allergovac Depot Group 2 Active	Allergovac Depot	-
Allergovac Depot Group 3 Active	Allergovac Depot	-
Allergovac Depot Group 5 Active	Allergovac Depot	-
Allergovac Depot Group 4 Active	Allergovac Depot	-

Primary Outcome Measures

Name	Time	Method
Variation of the Concentration of Phleum Pratense Extract Needed to Produce a Positive Nasal Provocation Test From Baseline (V0) to Final Visit (FV).	Baseline (V0) and Final Visit (FV). The Final Visit will be conducted within 7 plus minus 2 days after the last dose is administered. The study will be carried out outside the pollination season of Phleum pratense.	Variation of the concentration of Phleum pratense extract needed to produce a positive nasal provocation test from baseline (V0) to final visit (FV). The changes will be compared among groups (including the placebo group).

Secondary Outcome Measures

Name	Time	Method
All Adverse Reactions and or Events Will be Recorded Both by the Patient and the Health Care Personnel Responsible for the Administration of the Subcutaneous Immunotherapy.	From baseline (V0) to final visit (VF). The Final Visit will be conducted within 7 plus minus 2 days after the last dose is administered. All AE should be monitored until they are satisfactorily resolved or stabilized after the final visit of the study	All adverse reactions and/or events were recorded both by the patient and the health care personnel responsible for the administration of the subcutaneous immunotherapy. The incidence and intensity of adverse events was compared among the treatment groups.

Trial Locations

Locations (10)

Hospital Universitario La Paz; 🇪🇸 Madrid, Spain

Hospital Universitario Gregorio Marañón; 🇪🇸 Madrid, Spain

Hospital Universitario Puerta de Hierro; 🇪🇸 Madrid, Spain

Hospital Universitario Ramón y Cajal; 🇪🇸 Madrid, Spain

Centro Hospitalar de S. João; 🇵🇹 Porto, Portugal

Instituto CUF Porto; 🇵🇹 Senhora da Hora, Portugal

Hospital da Universidade de Coimbra; 🇵🇹 Coimbra, Portugal

Centro Hospitalar de Setúbal - Hospital de São Bernardo; 🇵🇹 Setúbal, Portugal

Centro Hospitalar Gaia/Espinho; 🇵🇹 Vila Nova de Gaia, Portugal

Hospital Ntra. Sra. del Prado; 🇪🇸 Talavera de la Reina, Toledo, Spain