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TR

triamcinolone (Trivaris / Trivaris)

✓ Approved

Merck & Co. · NR3C1 · Small Molecule

What is triamcinolone?

triamcinolone is a small molecule developed by Merck & Co.. It is approved for therapeutic indications via others or injectable (others) or intraocular injection.

Drug Profile

Brand NamesTrivaris, Trivaris
CompanyMerck & Co.
Drug ClassSmall Molecule
Molecular TargetNR3C1
RouteOthers, Injectable (Others), Intraocular Injection
StatusApproved

Mechanism of Action

Molecular Targets

triamcinolone acts on 1 molecular target:

NR3C1nuclear receptor subfamily 3 group C member 1 (GR, GCCR)
Want deeper analysis?Noah AI can explain complex mechanisms and compare to similar drugs.

Therapeutic Indications

triamcinolone is developed for 5 unique indications across 1 therapeutic area.

Therapeutic AreaConditionPhase
Eye disordersDiabetic retinal oedema✓ Approved
Eye disordersDiabetic retinopathy✓ Approved
Eye disordersRetinal vein occlusion✓ Approved
Eye disordersUveitis✓ Approved
Eye disordersCystoid macular oedema✓ Approved

Related Research Articles

PubMedNepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH2026-10-14

Management of Adult-onset Eyelid Xanthogranuloma: Debulking Surgery Coupled with Intralesional Corticosteroids.

Kamaluddin Najmatuzzahra N, Pratiwi Andi A

Adult-onset xanthogranuloma (AOX) is a rare, benign inflammatory disorder within the spectrum of non-Langerhans cell histiocytosis, often manifesting as localised skin lesions in middle-aged adults and frequently misdiagnosed due to its nonspecific presentation. A 43-year-old woman developed a painless, progressively enlarging mass on her right upper eyelid over four months, with histopathology confirming AOX. Following surgical debulking and adjunctive intralesional corticosteroid (triamcinolone acetonide) injection, the patient exhibited significant clinical improvement and no recurrence at three months. This outcome supports emerging evidence that a combination of surgery and corticosteroid therapy effectively reduces lesion size and recurrence rates in localised AOX. The multimodal approach combining surgical excision and intralesional corticosteroid injections provides a conservative and effective management strategy for AOX, with favourable outcomes and minimal complications. Further research is warranted to standardise treatment protocols for this rare orbital disease.

PubMedPlastic and reconstructive surgery. Global open2026-10-14

Palatal Island Flap With Adjuvant Radiotherapy for Hard Palate Adenoid Cystic Carcinoma: 2-year Outcomes.

Ongkasuwan Pattana P

Adenoid cystic carcinoma (ACC) of the minor salivary glands most commonly arises in the hard palate and exhibits perineural invasion, indolent growth, and late recurrence, often requiring multimodal therapy. Reconstruction must restore oronasal separation, speech, and deglutition; data regarding the tolerance of palatal island flaps to postoperative radiotherapy and long-term functional outcomes remain limited. A 35-year-old woman with T1N0M0 ACC of the right hard palate (American Joint Committee on Cancer, 8th edition) underwent wide local excision with partial palatal ostectomy followed by reconstruction using a contralateral palatal island flap. After complete mucosal healing, adjuvant intensity-modulated radiotherapy (66 Gy in 33 fractions) was administered. Two-year outcomes were assessed using Thai-language validated versions of the EORTC QLQ-C30, EORTC QLQ-HN43, FACT-H&N, and UW-QOL questionnaires. Final pathology demonstrated cribriform and tubular ACC with perineural invasion. The tumor approached the medial (0.4 mm) and lateral (1.7 mm) margins, which were close but uninvolved. Acute toxicity consisted of grade 2 donor-site oral mucositis treated with topical triamcinolone. At 2-year follow-up, surveillance with magnetic resonance imaging of the skull base, computed tomography of the chest, and bone scintigraphy demonstrated no evidence of locoregional recurrence or distant metastasis. Speech was fully intelligible on speech-language pathology assessment, the Functional Oral Intake Scale score was 7, and quality-of-life outcomes remained favorable across all instruments. This case suggested that a palatal island flap may tolerate adjuvant radiotherapy when irradiation is delivered after complete flap healing, with favorable oncological, functional, and quality-of-life outcomes at 2 years.

PubMedFrontiers in ophthalmology2026-10-14

Orbital decompression with intraorbital corticosteroid injection during the active phase of thyroid eye disease: outcomes in a real-world cohort.

Neuhouser Adam J AJ, Skender Sarah S, Spadaro Jane Z JZ, Kahana Alon A

Orbital decompression is an effective surgery for reducing orbital congestion and proptosis for patients with thyroid eye disease (TED). However, it is commonly stated that elective orbital decompression, i.e., for reasons other than compressive optic neuropathy, should await the quiescent phase of the disease. The reason is to avoid inducing a flare-up of the orbitopathy secondary to surgical inflammation. Still, this means that patients with moderate to severe TED who are suffering from symptoms associated with TED must wait months to years before initiating surgical treatment. The purpose of this study is to evaluate the effectiveness of orbital apex decompression combined with intraorbital corticosteroid injection in patients with active TED, defined as Clinical Activity Score (CAS) ≥3. This retrospective, single-center cohort study included patients with active TED (pre-operative CAS ≥ 3) who underwent single or staged orbital decompression between February 2023 and September 2025. All lateral wall decompressions included an intraorbital injection of a combination triamcinolone and dexamethasone as part of the operative technique. Primary outcomes included change in CAS, change in proptosis, and postoperative disease progression (≥ 2-point increase in CAS at ≥ 8 weeks). Secondary analysis compared outcomes in patients with and without perioperative treatment using disease-modifying therapy (DMT). Thirty-six patients met inclusion criteria; 14 had preoperative dysthyroid optic neuropathy. Mean CAS decreased from 4.7 to 1.6 (Δ -3.1; 95% CI -3.92 to -2.36), and mean proptosis decreased from 22.7 mm to 19.7 mm (Δ -3.0 mm; 95% CI -3.28 to -2.23). One patient with severe TED met criteria for postoperative disease progression. Outcomes were consistent across subgroups regardless of perioperative DMT exposure. No patients developed new-onset diplopia. Orbital decompression combined with intraorbital corticosteroid injection during active TED was associated with clinically meaningful reductions in CAS and proptosis, with infrequent postoperative deterioration and no major surgical complications. These findings provide real-world evidence supporting use of this combined approach during active disease, including in patients without dysthyroid optic neuropathy. These results are specific to a particular surgical technique and to the perioperative management of underlying thyroid status and risk factors associated with TED exacerbation.

PubMedMolecular biotechnology2026-10-13

Retraction Note: Triamcinolone Acetonide Produced by Bacillus velezensis YEBBR6 Exerts Antagonistic Activity Against Fusarium oxysporum f. sp. Cubense: A Computational Analysis.

Nayana R U Krishna RUK, Nakkeeran S S, Saranya N N, Saravanan R R et al.

PubMedJournal of pharmaceutical sciences2026-10-13

Enzymatically degalactosylated xyloglucan in situ gels for topical delivery of triamcinolone acetonide.

Silva Luis F C LFC, Lemos-Senna Elenara E, Borsali Redouane R, Halila Sami S

Thermoresponsive in situ gelling systems are attractive platforms for topical ocular delivery because they can be administered as liquids and rapidly form gels at the ocular surface, thereby increasing residence time and sustaining drug release. This study investigated whether enzymatic degalactosylation of tamarind-seed xyloglucan could be used to develop thermoresponsive hydrogels for the delivery of triamcinolone acetonide (TA). Degalactosylation kinetics, monitored by monosaccharide analysis and oligosaccharide profiling, showed rapid initial galactose removal followed by a plateau near 50%. This structural evolution modified xyloglucan oligosaccharide motifs and induced thermoresponsive gelation after substantial degalactosylation. Among the modified samples, Deg50-XG showed the most suitable thermal transition. At 3.0% (w/v), it gelled at 35°C within about 68 s and formed the strongest elastic network. Contact with simulated tear fluid was found to be a second, independent gelation trigger: at an identical polymer concentration of 1.5% (w/v), the sol-gel transition shifted from 36.4°C in water to 25.7°C, i.e. from above to well below ocular surface temperature, and an elastic network with a storage modulus approximately three orders of magnitude higher was formed at 35°C. In vitro release studies showed that increasing polymer concentration slowed TA release and reduced dissolution efficiency, consistent with denser hydrogel networks. Kinetic analysis indicated that the relative contribution of network relaxation and erosion to drug transport increased with polymer concentration, while release remained consistent with a matrix containing dispersed, poorly soluble drug. These results show that controlled enzymatic tailoring of xyloglucan can be used to tune gelation behavior and drug-release performance in dually thermo- and ion-triggered thermoresponsive in situ gelling systems for sustained topical delivery of TA.

PubMedCurrent medicinal chemistry2026-10-13

Endoplasmic Reticulum Stress Drives Carotid Atherosclerotic Plaque Instability: Integrative Insights into Biomarkers and Therapeutic Targets.

Zhou Haifeng H, Zhang Zhiwei Z, Huang Jianhuang J, Ding Zhanghui Z

Carotid atherosclerosis is a leading cause of stroke, with plaque rupture closely linked to endoplasmic reticulum stress (ERS). However, the precise mechanisms of ERS in plaque instability remain incompletely understood. This study aims to investigate the role of ERS in carotid plaque instability, identify potential biomarkers, and screen candidate therapeutic drugs. Transcriptomic data from the Gene Expression Omnibus (GEO) database (GSE43292 and GSE163154) were analyzed using differential expression analysis, weighted gene co-expression network analysis (WGCNA), and machine learning approaches (Elastic Net, RFE-SVM, GBM) to identify ERS-related differentially expressed genes (ERS-DEGs). The expression, apoptosis, and inflammatory responses of ERS marker genes were validated using qRT-PCR, flow cytometry, and ELISA. CIBERSORT was employed to assess immune cell infiltration, and the Enrichr database was used for drug prediction. Four ERS marker genes (TFRC, APOE, NLRP3, NOD2) were identified, showing significantly higher expression in the unstable plaque model (ox-LDL+TNF-α) compared to the stable model (p<0.01), with NLRP3 upregulation being particularly pronounced. Knockdown of these genes significantly reduced apoptosis rates and IL-1β/IL-6 secretion in HUVECs and THP-1-derived macrophages in the unstable model (p<0.01). Immune cell infiltration analysis revealed increased M0 macrophage abundance and decreased CD8+ T cell presence in unstable plaques. Drug prediction identified Bupropion and Triamcinolone as candidate drugs with potential therapeutic value. ERS drives carotid plaque instability by regulating inflammation and apoptosis. The identified marker genes serve as potential biomarkers, offering novel targets for the diagnosis and treatment of atherosclerosis. The candidate drugs provide directions for future clinical interventions. This study suggests that ERS contributes to carotid plaque instability and identifies TFRC, APOE, NLRP3, and NOD2 as genes of interest with potential diagnostic value. Bupropion and triamcinolone emerged as in silico predicted compounds warranting further investigation. These findings provide exploratory insights into ERS in human carotid atherosclerosis and highlight directions for future studies.

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