TheraRadar
Data updated: May 26, 2026

NOCTIVA (desmopressin acetate)

Rare Disease Approved 2017-03-03
1
Indication
--
Phase 3 Trials
9
Years on Market

Details

Status
Discontinued
First Approved
2017-03-03
Patent Cliff
2030

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Patent cliff and revenue data

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Routes
NASAL
Dosage Forms
SPRAY, METERED

Companies

Active Ingredient: DESMOPRESSIN ACETATE

NOCTIVA Approval History

2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
2 FDA actions from 2017 to 2017
Mar 2017 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer

What NOCTIVA Treats

1 FDA approvals

Originally approved for its first indication in 2017 .

  • Other (1)
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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.

NOCTIVA FDA Label Details

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3 OB patents · 1 families · 60 international docs across 15 countries

NOCTIVA Patents & Exclusivity

Latest Patent: Jun 2030

Patents (3 active)

US11419914 Expires Jun 15, 2030
US12090190 Expires Jun 15, 2030
US9539302 Expires Jun 15, 2030
Source: FDA Orange Book

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Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2030
  • 12 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • Competitor tracking
  • Same target/indication analysis
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Data Sources

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