TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

BETHKIS

TOBRAMYCIN
Infectious Disease Approved 2012-10-12
1
Indication
--
Phase 3 Trials
13
Years on Market

Details

Status
Prescription
First Approved
2012-10-12
Routes
INHALATION
Dosage Forms
SOLUTION

Companies

Active Ingredient: TOBRAMYCIN

BETHKIS Approval History

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What BETHKIS Treats

1 indications

BETHKIS is approved for 1 conditions since its original approval in 2012. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Cystic Fibrosis
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.

BETHKIS FDA Label Details

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Indications & Usage

FDA Label (PDF)

BETHKIS is indicated for the management of cystic fibrosis patients with Pseudomonas aeruginosa . Safety and efficacy have not been demonstrated in patients under the age of six years, patients with FEV 1 less than 40% or greater than 80% predicted, or patients colonized with Burkholderia cepacia [see Clinical Studies ] . BETHKIS is an inhaled aminoglycoside antibacterial indicated for the management of cystic fibrosis patients with Pseudomonas aeruginosa . Safety and efficacy have not been demonstrated in patients under the age of six years, patients with a forced expiratory volume in one sec...

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Data Sources

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