TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

BYDUREON BCISE

EXENATIDE SYNTHETIC
Approved 2017-10-20
4
Indications
--
Phase 3 Trials
1
Priority Reviews
8
Years on Market

Details

Status
Discontinued
First Approved
2017-10-20
Routes
SUBCUTANEOUS
Dosage Forms
SUSPENSION, EXTENDED RELEASE

Companies

Active Ingredient: EXENATIDE SYNTHETIC

BYDUREON BCISE Approval History

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What BYDUREON BCISE Treats

4 FDA approvals

Originally approved for its first indication in 2017 . Covers 4 distinct patient populations.

  • Other (4)
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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.

BYDUREON BCISE FDA Label Details

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BYDUREON BCISE Patents & Exclusivity

Latest Patent: Apr 2031

Patents (47 active)

US8895033*PED Expires Apr 4, 2031
US8895033 Expires Oct 4, 2030
US8361972*PED Expires Sep 21, 2028
US8361972 Expires Mar 21, 2028
US8501698*PED Expires Dec 20, 2027
US8501698 Expires Jun 20, 2027
US8906851*PED Expires Feb 18, 2027
US8329648*PED Expires Feb 18, 2027
US9884092*PED Expires Feb 18, 2027
US8329648 Expires Aug 18, 2026
+ 37 more patents
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.