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Antihistamine
Mometasone + Azelastine, then Mometasone Furoate, then Azelastine Hydrochloride for Hay Fever
Phase 1
Waitlist Available
Research Sponsored by Sandoz
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from time 0 hours (prior to dosing), up to 48 or 72 hours post dose
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new treatment that combines two medications, mometasone furoate and azelastine hydrochloride. It targets adolescents and young adults who suffer from seasonal allergies. The treatment aims to reduce swelling and stop allergic reactions more effectively than using each medication alone.
Eligible Conditions
- Hay Fever
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from time 0 hours (prior to dosing), up to 48 or 72 hours post dose
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from time 0 hours (prior to dosing), up to 48 or 72 hours post dose
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
AUCinf
AUCt
Cmax
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Group I: Mometasone Furoate, then Azelastine Hydrochloride, then Mometasone + AzelastineExperimental Treatment3 Interventions
Group II: Mometasone + Azelastine, then Mometasone Furoate, then Azelastine HydrochlorideExperimental Treatment3 Interventions
Group III: Azelastine Hydrochloride, then Mometasone + Azelastine, then Mometasone FuroateExperimental Treatment3 Interventions
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mometasone Furoate
2005
Completed Phase 4
~190
Azelastine Hydrochloride
2021
Completed Phase 3
~210
Find a Location
Who is running the clinical trial?
SandozLead Sponsor
143 Previous Clinical Trials
26,237 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have had a bad reaction or allergy to mometasone, azelastine, or other similar medications.You have used tobacco or nicotine products within the past 6 months before the study.You have a nose piercing or septum piercing.You are a young person who doesn't smoke and have seasonal allergies causing a runny or stuffy nose.
Research Study Groups:
This trial has the following groups:- Group 1: Mometasone + Azelastine, then Mometasone Furoate, then Azelastine Hydrochloride
- Group 2: Mometasone Furoate, then Azelastine Hydrochloride, then Mometasone + Azelastine
- Group 3: Azelastine Hydrochloride, then Mometasone + Azelastine, then Mometasone Furoate
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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