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triamcinolone acetonide

Generic: TRIAMCINOLONE ACETONIDE·Brand: ALLERNAZE, ARISTOCORT, ARISTOCORT A, ARISTOGEL, AZMACORT, FLUTEX, KENALOG, KENALOG IN ORABASE, KENALOG-10, KENALOG-40, KENALOG-80, KENALOG-H, NASACORT, NASACORT ALLERGY 24 HOUR, NASACORT HFA, ORALONE, TRIACET, TRIACORT, TRIAMCINOLONE ACETONIDE, TRIANEX, TRIATEX, TRIDERM, TRIESENCE, TRIVARIS, TRYMEX, XIPERE, ZILRETTA

triamcinolone acetonide: sourced relationships with 2 companies · 8 clinical trials tracked · 3 FDA decisions.

triamcinolone acetonide evidence translation

What we can confirm

3 FDA records · 8 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 triamcinolone acetonide, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence3 indications · 1 study sponsors

Related indications

Uses temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • sneezing • itchy noseAlopecia AreataAtopic Dermatitis
Dated Pipeline Records (2)
CompanyDated record stage
PERRIGO Co plc (PRGO)
Reported 2009-07-30 · Current development: unknownSource
Uses temporarily relieves these symptoms of hay fever or oth…
Approved
DR REDDYS LABORATORIES LTD (RDY)
Reported 2025-03-12 · Current development: unknownSource
Approved
Clinical Trial Registry Records (8)

Evaluation of UV-Trichoscopic Red Fluorescence Intensity in Relation to Trichoscopic Findings and Response to Intralesional Corticosteroid Treatment in Limited Plaque-Type Alopecia Areata

NCT07803874Registry updated 2026-09-11
Recruiting

Primary endpoint: Association Between Baseline UV-Trichoscopic Red Fluorescence Intensity and Timing of First Visible Hair Regrowth

Observational40 targetStarted 2026-07Completion 2026-121 site · Turkey (Türkiye)Istanbul Training and Research Hospital

A Phase 3, Prospective, Multicenter, Randomized, Parallel-Arm, Double-Masked, Placebo-Controlled Study Evaluating the Safety and Efficacy of TRIESENCE® (Injectable Suspension) for the Treatment of Ocular Inflammation and Pain After Ophthalmic Surgery

NCT07832552Registry updated 2026-09-22·Phase 3·HROW
Enrolling by invitation

Primary endpoint: Proportion of Subjects With No Anterior Chamber Cells (Grade 0) at Day 14

InterventionalRandomizeddouble250 targetStarted 2026-05Completion 2027-031 site · United StatesHarrow Inc

The Effect of Topical Triamcinolone Acetonide Application on Wound Healing in the Palatal Donor Site Following Free Gingival Graft Surgery

NCT07409571Registry updated 2026-02-13·N/A
Recruiting

Primary endpoint: Oral Health-Related Quality of Life

InterventionalRandomizeddouble34 targetStarted 2026-01Completion 2026-031 site · Turkey (Türkiye)Kahramanmaras Sutcu Imam University

Comparison of Ultrasound-Guided Triamcinolone Injection and Transcutaneous Electrical Nerve Stimulation for the Treatment of Long Head of the Biceps Brachii Tendinopathy

NCT07817433Registry updated 2026-09-14·N/A
Completed

Primary endpoint: Visual Analog Scale (VAS) for Pain

InterventionalRandomizedopen42 enrolledStarted 2025-01Completion 2026-021 site · Turkey (Türkiye)Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Comparison of the Outcome of Treatment of Intralesional Triamcinolone Acetonide With Intralesional Verapamil Hydrochloride in Patients Presenting With Keloid at Tertiary Care Hospital, Bahawalpur.

NCT07420166Registry updated 2026-02-19·N/A
Completed

Primary endpoint: Scar assessment

InterventionalRandomizedopen60 enrolledStarted 2025-01Completion 2025-061 site · PakistanMuhammad Aamir Latif

Evaluation of the Efficacy of Suprascapular Nerve Block in Adhesive Capsulitis: a Randomized Controlled Superiority Trial

NCT06176248Registry updated 2026-02-20·N/A
Recruiting

Primary endpoint: Constant score

InterventionalRandomizeddouble62 targetStarted 2024-10Completion 2027-031 site · FranceCHU de Reims

Longitudinal Endotyping Of Atopic Dermatitis Through Transcriptomic Skin Analysis (ADRN-12)

NCT05436535Registry updated 2026-02-19·Phase 4
Completed

Primary endpoint: Mild (EASI ≤ 7) vs. moderate-to-severe (EASI > 7) AD severity between type 2-high vs. type 2-low endotype from non-lesional skin transcriptome in the dupilumab-naïve AD adults and children.

Interventionalopen433 enrolledStarted 2022-11Completion 2025-1010 sites · United StatesNational Institute of Allergy and Infectious Diseases (NIAID)

Symptom Clusters in Children With Exacerbation-prone Asthma

NCT04002362Registry updated 2026-02-13·Phase 2
Completed

Primary endpoint: Change in Asthma Control Questionnaire (ACQ) Score

Interventionalopen68 enrolledStarted 2019-11Completion 2025-122 sites · United StatesEmory University
FDA Decisions3 records
ApprovalINDICATIONS AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including triamcinolone acetonide injectable suspension is indicated for intramuscular use as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reaction(RDY)FDA ↗
ANDA218421UNKNOWNStandardOtherInjectable
ApprovalINDICATIONS AND USAGE The intra-articular or soft tissue administration of triamcinolone acetonide injectable suspension is indicated as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis, acute and subacute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis, synovitis of osteoarthritis. The intralesional administration of triamcinolone acetonide injectable suspension is indicated for a(RDY)FDA ↗
ANDA218773UNKNOWNStandardOtherInjectable
ApprovalUses temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • sneezing • itchy nose(PRGO)FDA ↗
ANDA078104OtherSpray, Metered

Frequently asked questions

Which companies have sourced relationships with triamcinolone acetonide?

triamcinolone acetonide has dated SEC/FDA relationship records for PERRIGO Co plc, DR REDDYS LABORATORIES LTD.

How many clinical trials involve triamcinolone acetonide?

BioSniper tracks 8 clinical trials involving triamcinolone acetonide.

What is triamcinolone acetonide's latest FDA decision?

The most recent tracked FDA decision for triamcinolone acetonide is Approval for INDICATIONS AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including triamcinolone acetonide injectable suspension is indicated for intramuscular use as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reaction, dated April 11, 2025.