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NCT02092597COMPLETEDanonymous

Safety Evaluation of Adverse Reactions in Diabetes

Sponsor

Source record

Charles University, Czech Republic

Phase

Source record

Phase 4

Modality

AI-normalized

small molecule

Target

AI-normalized

Incretin receptors (GLP-1 and DPP-4) involved in glucose metabolism and cardiovascular, gastrointestinal, and renal functions.

Indication / condition

AI-normalized

Type 2 Diabetes Mellitus

Intervention

Source record

Exenatide, Linagliptin, Gliclazide

Source & freshness

Source record

NCT ID

NCT02092597

Original source

ClinicalTrials.gov

Source last updated

Feb 07, 2018

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT02092597

Title

Safety Evaluation of Adverse Reactions in Diabetes

Sponsor

Charles University, Czech Republic

Status

COMPLETED

Phase

Phase 4

Condition raw

Type 2 Diabetes Mellitus

Condition normalized

Type 2 Diabetes Mellitus

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Incretin receptors (GLP-1 and DPP-4) involved in glucose metabolism and cardiovascular, gastrointestinal, and renal functions.

Target normalized

Incretin receptors (GLP-1 and DPP-4) involved in glucose metabolism and cardiovascular, gastrointestinal, and renal functions.

Interventions

Exenatide, Linagliptin, Gliclazide

Public preview

Source record

The clinical trial, sponsored by Charles University, evaluates the safety and efficacy of incretin-based therapies (GLP-1 agonists and DPP-4 inhibitors) in patients with Type 2 diabetes mellitus. Given the increasing prevalence of diabetes and associated cardiovascular complications, this study could provide critical insights into the long-term safety profiles of these therapies, potentially influencing prescribing practices and market dynamics. The results may enhance the competitive positioning of existing therapies like Exenatide and Linagliptin against newer entrants in the diabetes treatment landscape. Furthermore, the findings could support claims for expanded indications or improved patient management strategies, thereby impacting market access and reimbursement considerations.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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