Company profile

TALPHERA, INC.

NASDAQ:TLPHBiotechnology: Pharmaceutical Preparations

Drug pipeline (1)

AssetStageRevenueTrialsStatus
SUFENTANILphase3—3no active trials

Revenue is the latest quarter the company reported for that product, from SEC filings; a fourth quarter is the year less nine months when no filing states one. Trial counts are of the product's ingredients, deduplicated by trial, so products sharing an ingredient share trials.

Clinical trials (17)

NCT IDPhaseStatusStartCompletionSponsor nameTitle
NCT02662556phase3completed2016-03-012016-06-01Talphera, IncA Multicenter, Open-Label Trial to Evaluate the Safety and Efficacy of the Sufentanil Sublingual Tablet 30 mcg in Patients With Post-Operative Pain
NCT01539642phase3completed2012-02-012013-01-01Talphera, IncA Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) for the Treatment of Post-Operative Pain in Patients After Open Abdominal Surgery
NCT01539538phase3completed2012-04-012012-12-01Talphera, IncA Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
NCT00612534phase2completed2008-03-012008-10-01Talphera, IncA Multicenter, Randomized, Placebo-Controlled Phase 2 Study to Evaluate the Clinical Efficacy, Safety, and Tolerability of ARX-F01 Sublingual Sufentanil in Patients Undergoing Elective Unilateral Total Knee Replacement
NCT00718081phase2completed2008-08-012009-03-01Talphera, IncA Multicenter, Randomized, Placebo-Controlled Phase 2 Study to Evaluate the Clinical Efficacy, Safety, and Tolerability of ARX-F01 Sublingual Sufentanil in Patients Undergoing Major Abdominal Surgery

FDA applications (0)

No records yet.