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Study Of Adults And Adolescents With Vasomotor Rhinitis

GlaxoSmithKline (GSK) logo

GlaxoSmithKline (GSK)

Status and phase

Completed
Phase 3

Conditions

Rhinitis, Vasomotor

Treatments

Drug: GW685698X

Study type

Interventional

Funder types

Industry

Identifiers

NCT00117325
FFR30006

Details and patient eligibility

About

The primary objective of this study is to compare the efficacy and safety of GW685698X 100mcg once daily (QD) aqueous nasal spray with vehicle placebo nasal spray in adult and adolescent subjects (12 years of age and older) with vasomotor rhinitis (VMR).

Enrollment

352 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Must be outpatients.
  • Diagnosis of VMR.
  • Literate in English or native language.

Exclusion criteria

  • Significant concomitant medical condition.
  • Use corticosteroids or other allergy medications during the study.
  • Used tobacco products within the past year.

Trial design

352 participants in 1 patient group

GW685698X
Experimental group
Description:
GW685698X
Treatment:
Drug: GW685698X

Trial contacts and locations

53

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Data sourced from clinicaltrials.gov

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