TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

VELTASSA

PATIROMER SORBITEX CALCIUM
Approved 2015-10-21
3
Indications
--
Phase 3 Trials
10
Years on Market

Details

Status
Discontinued
First Approved
2015-10-21
Routes
ORAL
Dosage Forms
POWDER

Companies

Active Ingredient: PATIROMER SORBITEX CALCIUM

VELTASSA Approval History

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What VELTASSA Treats

3 FDA approvals

Originally approved for its first indication in 2015 . Covers 3 distinct patient populations.

  • Other (3)
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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.

VELTASSA FDA Label Details

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VELTASSA Patents & Exclusivity

Latest Patent: Oct 2033
Exclusivity: Oct 2026

Patents (112 active)

US9492476 Expires Oct 8, 2033
US9925212 Expires Oct 8, 2033
US11123363 Expires Oct 8, 2033
US8337824 Expires May 29, 2030
US8147873 Expires Jun 20, 2028
US8282913 Expires May 29, 2027
US8216560 Expires Mar 14, 2027
+ 102 more patents

Exclusivity

NPP Until Oct 2026
NPP Until Oct 2026
NPP Until Oct 2026
NS Until Oct 2026
NPP Until Oct 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.