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Clinical trial intelligence report
A Double-Blind, Randomized, Parallel Group Comparison of the Effects of FX006 and TCA IR (Triamcinolone Acetonide Suspension) on Blood Glucose in Patients With Osteoarthritis of the Knee and Type 2 Diabetes Mellitus
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02762370-Jul 28, 2026
NCT ID
NCT02762370
Status
COMPLETED
Phase
Phase 2
Sponsor
Pacira Pharmaceuticals, Inc
Executive brief
Investment-Ready Snapshot
FX006, developed by Pacira Pharmaceuticals, aims to provide a safer alternative to traditional corticosteroids for patients with osteoarthritis of the knee and type 2 diabetes mellitus. The market for osteoarthritis treatments is significant, with increasing demand for effective pain management solutions. The results from this trial suggest FX006 may have a favorable safety profile regarding blood glucose levels compared to immediate-release triamcinolone acetonide (TCA IR), potentially positioning it as a competitive option in the market. Diligence should focus on the regulatory pathway and potential market access strategies, as well as the competitive landscape, particularly against established corticosteroid therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02762370
Indication
Osteoarthritis of the Knee
Modality
small molecule
Target
FX006 is an extended-release formulation of triamcinolone acetonide, targeting inflammation and pain associated with osteoarthritis through intra-articular administration.
Intervention
FX006 32 mg, TCA IR 40 mg
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.