TrialSignal
Clinical trial intelligence report
Study 200977: Albiglutide + Insulin Glargine Versus Insulin Lispro + Insulin Glargine in the Treatment of Subjects With Type 2 Diabetes Mellitus: The Switch Study
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 20, 2026
NCT ID
NCT02229227
Status
COMPLETED
Phase
Phase 3b
Sponsor
GlaxoSmithKline
Executive brief
Investment-Ready Snapshot
The Switch Study evaluates the efficacy and safety of albiglutide, a GLP-1 receptor agonist, in combination with insulin glargine for patients with Type 2 Diabetes Mellitus (T2DM) inadequately controlled on a basal-bolus insulin regimen. Given the increasing prevalence of T2DM and the demand for effective treatment options, this study positions GlaxoSmithKline (GSK) to strengthen its portfolio in the diabetes market. The competitive landscape includes established therapies such as insulin lispro and other GLP-1 receptor agonists, which may pose challenges in market penetration. Successful outcomes could enhance GSK's market share and provide leverage in negotiations with payers. Diligence should focus on the safety profile and potential for adverse events, particularly hypoglycemia, which could impact market acceptance.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02229227
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
Glucagon-like peptide-1 receptor (GLP-1R)
Intervention
Albiglutide, Insulin Glargine and Insulin Lispro
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.