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Clinical Trials/NCT01700192
NCT01700192
Completed
Phase 3

A One-year Placebo-Controlled Study Evaluating the Efficacy and Safety of the House Dust Mite Sublingual Allergen Immunotherapy Tablet (SCH 900237/MK 8237) in Children and Adult Subjects With House Dust Mite-Induced Allergic Rhinitis/Rhinoconjunctivitis With or Without Asthma (Protocol No. P05607/001)

ALK-Abelló A/S0 sites1,482 target enrollmentJanuary 2013

Overview

Phase
Phase 3
Intervention
MK-8237 tablets
Conditions
Rhinitis, Allergic, Perennial
Sponsor
ALK-Abelló A/S
Enrollment
1482
Primary Endpoint
Number of Participants Who Experience At Least One Adverse Event (AE)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to assess the efficacy and safety of MK-8237 (SCH 900237) in the treatment of House Dust Mite (HDM)-Induced Allergic Rhinitis/Rhinoconjunctivitis (AR/ARC) in children and adults.

The primary hypothesis of this study is that administration of MK-8237, compared to placebo, results in significant reduction in the average total combined rhinitis score (TCRS).

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
April 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • History of AR/ARC to house dust of 1 year duration or more (with or without asthma)
  • If female of childbearing potential, has a negative urine pregnancy test at Screening and agrees to remain abstinent or use (or have their partner use) an acceptable method of birth control within the projected duration of the study
  • Able to read, understand and complete questionnaires and diaries

Exclusion Criteria

  • Clinically relevant history of symptomatic ARC caused by animal dander, molds and/or cockroach (e.g. present in the home, job, daycare, etc.) or other perennial allergen
  • History of symptomatic seasonal ARC and/or asthma due to an allergen to which the participant is sensitized and regularly exposed
  • Nasal condition that could confound the efficacy or safety assessments (e.g., nasal polyposis)
  • Received an immunosuppressive treatment within 3 months prior to screening
  • Unstable or severe asthma, or has experienced a life-threatening asthma attack or an occurrence of any clinical deterioration of asthma that resulted in emergency treatment, hospitalization due to asthma, or treatment with systemic corticosteroids (but allowing short-acting beta agonists \[SABAs\]) at any time within 3 months prior to screening
  • Asthma requiring high-dose inhaled corticosteroids (ICS) within 6 months prior to screening
  • History of anaphylaxis with cardiorespiratory symptoms with prior immunotherapy, unknown cause or inhalant allergen
  • History of chronic urticaria and/or angioedema within 2 years prior to screening
  • History of chronic sinusitis during 2 years prior to screening
  • Pregnant, breastfeeding, or expecting to conceive within the projected duration of the study

Arms & Interventions

MK-8237

MK-8237 12 Development Units (DU) rapidly dissolving tablets administered sublingually once daily (q.d.).

Intervention: MK-8237 tablets

Placebo

Placebo to MK-8237 rapidly dissolving tablets administered sublingually q.d.

Intervention: Placebo tablets

Outcomes

Primary Outcomes

Number of Participants Who Experience At Least One Adverse Event (AE)

Time Frame: Up to 54 weeks

An AE is defined as any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment.

Average Total Combined Rhinitis Score (TCRS) During Last 8 Weeks of Treatment

Time Frame: Last 8 weeks of treatment (Weeks 44 to 52)

The TCRS is the sum of the rhinitis Daily Symptom Score (DSS; range: 0 to 12) and the rhinitis Daily Medication Score (DMS; range: 0 to 12); the total possible TCRS ranges from 0 to 24 points with higher scores indicative of greater symptom severity. The endpoint was calculated as the average daily diary entry score from the last 8 weeks of treatment.

Number of Participants Who Discontinue Study Drug Due to an AE

Time Frame: Up to 52 weeks

An AE is defined as any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment.

Secondary Outcomes

  • Average Rhinitis Daily Symptom Score (Rhinitis DSS) During Last 8 Weeks of Treatment(Last 8 weeks of treatment (Weeks 44 to 52))
  • Average Allergic Rhinitis/Rhinoconjunctivitis Symptoms Assessed by Visual Analogue Scale (VAS) During Last 8 Weeks of Treatment(Last 8 weeks of treatment (Weeks 44 to 52))
  • Average Rhinitis Daily Medication Score (Rhinitis DMS) During Last 8 Weeks of Treatment(Last 8 weeks of treatment (Weeks 44 to 52))
  • Average Total Combined Rhinoconjunctivitis Score (TCS) During Last 8 Weeks of Treatment(Last 8 weeks of treatment (Weeks 44 to 52))

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