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minocycline

Generic: MINOCYCLINE HYDROCHLORIDE·Brand: AMZEEQ, ARESTIN, Amzeeq, Arestin, DYNACIN, EMROSI, Emrosi, MINOCIN, MINOCYCLINE HYDROCHLORIDE, MINOLIRA, SOLODYN, XIMINO, ZILXI, Zilxi

minocycline: sourced relationships with 2 companies · 4 clinical trials tracked · 3 FDA decisions.

minocycline evidence translation

What we can confirm

3 FDA records · 4 tracked trials

What it means

More than one company relationship is source-backed. Until you choose one, AI stays drug-only and does not guess ownership.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

What is verified about minocycline, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 0 study sponsors

Related indications

Inflammatory lesions of rosacea in adultsCystic FibrosisStrokeTraumatic Brain Injury

Study sponsors

No additional listed-company sponsor is linked.

Dated Pipeline Records (2)
CompanyDated record stage
Bausch Health Companies Inc. (BHC)
Reported 2006-05-08 · Current development: unknownSource
Approved
Journey Medical Corp (DERM)
owner · Reported 2024-03-29 · Current development: unknownSource
Inflammatory lesions of rosacea in adults
Approved
Clinical Trial Registry Records (4)

Effect of Oral Minocycline in Patients With Acute Stroke - a Randomized, Open Label, Prospective Trial

NCT07237048Registry updated 2026-02-11·Phase 2
Recruiting

Primary endpoint: Change in National Institutes of Health Stroke Scale (NIHSS) Score at Day 7 post stroke

InterventionalRandomizedsingle1,164 targetStarted 2026-02Completion 2028-121 site · United StatesJoyce Chen

Multi-Arm Multi-Stage Adaptive Platform Trial (APT) for the Acute Treatment of Traumatic Brain Injury

NCT05826912Registry updated 2025-12-22·Phase 2
Enrolling by invitation

Primary endpoint: Change in Glasgow Outcome Scale-Extended (GOSE 2-Way)

InterventionalRandomizedquadruple672 targetStarted 2024-08Completion 2029-0818 sites · United StatesUniversity of California, San Francisco

A Phase 2, Open-Label, Randomized Trial Evaluating the Impact of Enhanced Versus Standard Dermatologic Management on Selected Dermatologic Adverse Events Among Patients With Locally Advanced or Metastatic EGFR-Mutated NSCLC Treated First-Line With Amivantamab + Lazertinib

NCT06120140Registry updated 2026-09-25·Phase 2
Active, not recruiting

Primary endpoint: Number of Participants With Grade Greater Than or Equal to (>=) 2 Dermatologic Adverse Events of Interest (DAEIs) Within 12 Weeks After Initiation of Anticancer Treatment

InterventionalRandomizedopen305 enrolledStarted 2024-02Completion 2030-0650 sites · Argentina, Brazil, China, United StatesJanssen Research & Development, LLC

STaph Aureus Resistance-Treat Early and Repeat (STAR-TER)

NCT03489629Registry updated 2026-02-17·Phase 2
Completed

Primary endpoint: Proportion of STAR-TER subjects with a negative MRSA culture at Day 28 vs. observational arm of historic STAR-Too trial

Interventionalopen37 enrolledStarted 2018-04Completion 2026-019 sites · United StatesUniversity of North Carolina, Chapel Hill
FDA Decisions3 records
Approval1 INDICATIONS AND USAGE ZILXI is indicated for the treatment of inflammatory lesions of rosacea in adults [see Clinical Studies ( 14 )] . Limitations of Use This formulation of minocycline has not been evaluated in the treatment of infections. To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, ZILXI should be used only as indicated [see Warnings and Precautions ( 5.14 )] . ZILXI is a tetracycline-class drug indicated for the treatment of inflammatory lesions of rosacea in adults. ( 1 ) Limitations of Use This formulation of minocycline has not been evaluated in the treatment of infections. To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, ZILXI should be used only as indicated ( 1 ).(DERM)FDA ↗
NDA213690Type 5 - New Formulation or New ManufacturerStandardTopicalAerosol, Foam
NDA201922Type 3 - New Dosage FormStandardOralCapsule, Extended Release
Approval(BHC)FDA ↗
NDA050808Type 3 - New Dosage FormStandardOralTablet, Extended Release

Frequently asked questions

Which companies have sourced relationships with minocycline?

minocycline has dated SEC/FDA relationship records for Bausch Health Companies Inc., Journey Medical Corp.

How many clinical trials involve minocycline?

BioSniper tracks 4 clinical trials involving minocycline.

What is minocycline's latest FDA decision?

The most recent tracked FDA decision for minocycline is Approval for 1 INDICATIONS AND USAGE ZILXI is indicated for the treatment of inflammatory lesions of rosacea in adults [see Clinical Studies ( 14 )] . Limitations of Use This formulation of minocycline has not been evaluated in the treatment of infections. To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, ZILXI should be used only as indicated [see Warnings and Precautions ( 5.14 )] . ZILXI is a tetracycline-class drug indicated for the treatment of inflammatory lesions of rosacea in adults. ( 1 ) Limitations of Use This formulation of minocycline has not been evaluated in the treatment of infections. To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, ZILXI should be used only as indicated ( 1 )., dated May 28, 2020.