TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

SPIRIVA

TIOTROPIUM BROMIDE
Respiratory Approved 2004-01-30
2
Indications
--
Phase 3 Trials
22
Years on Market

Details

Status
Prescription
First Approved
2004-01-30
Routes
INHALATION
Dosage Forms
POWDER

Companies

Active Ingredient: TIOTROPIUM BROMIDE

SPIRIVA Approval History

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What SPIRIVA Treats

3 indications

SPIRIVA is approved for 3 conditions since its original approval in 2004. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Chronic Obstructive Pulmonary Disease
  • Chronic Bronchitis
  • Emphysema
Source: FDA Label

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

SPIRIVA FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

STIOLTO RESPIMAT is a combination of tiotropium bromide, an anticholinergic and olodaterol, a long-acting beta 2 -adrenergic agonist (LABA) indicated for the long-term, once-daily maintenance treatment of patients with chronic obstructive pulmonary disease (COPD). Important limitations: STIOLTO RESPIMAT is NOT indicated to treat acute deterioration of COPD. STIOLTO RESPIMAT is NOT indicated to treat asthma. 1.1 Maintenance Treatment of COPD STIOLTO RESPIMAT is a combination of tiotropium bromide and olodaterol indicated for long-term, once-daily maintenance treatment of patients with chronic o...

SPIRIVA Patents & Exclusivity

Latest Patent: Jul 2026

Patents (2 active)

US8022082*PED Expires Jul 19, 2026
US8022082 Expires Jan 19, 2026
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.