drugset / Trial / NCT01614691

Safety and Efficacy of SPARC1203 in Allergic Rhinitis

NCT01614691 ↗

Phase 2 Completed 159 enrolled Sun Pharma Advanced Research Company Limited
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will assess safety and efficacy of SPARC1203 delivered via nasal spray in patients with allergic rhinitis

Timeline

Start
2012-06
Primary completion
2012-11
Completion
2013-03

Outcome

Met primary endpoint

paper Statistically significant improvements in TNSS from baseline to days 15 and 16 were observed with all S0597 doses vs placebo (P = .0005 overall) PMID 26272281 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject SPARC1203 Unknown 200 ug Intranasal
Subject SPARC1203 Unknown 400 ug Intranasal
Subject SPARC1203 Unknown 800 ug Intranasal

Indications