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NCT01606397COMPLETEDanonymous

The Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of Multiple Escalating Doses of LY2409021 in Patients With Type 2 Diabetes Mellitus

Sponsor

Source record

Eli Lilly and Company

Phase

Source record

Phase 1

Modality

AI-normalized

small molecule

Target

AI-normalized

Glucagon receptor antagonist

Indication / condition

AI-normalized

Diabetes Mellitus, Type 2

Intervention

Source record

Placebo, LY2409021

Source & freshness

Source record

NCT ID

NCT01606397

Original source

ClinicalTrials.gov

Source last updated

May 25, 2012

Ingested at

Jun 16, 2026

Internal sync

Jun 16, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
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NCT ID

NCT01606397

Title

The Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of Multiple Escalating Doses of LY2409021 in Patients With Type 2 Diabetes Mellitus

Sponsor

Eli Lilly and Company

Status

COMPLETED

Phase

Phase 1

Condition raw

Diabetes Mellitus, Type 2

Condition normalized

Diabetes Mellitus, Type 2

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Glucagon receptor antagonist

Target normalized

Glucagon receptor antagonist

Interventions

Placebo, LY2409021

Public preview

Source record

LY2409021, developed by Eli Lilly and Company, is positioned as a novel therapeutic option for managing Type 2 Diabetes Mellitus through glucagon receptor antagonism. The diabetes market is highly competitive, with established players like Novo Nordisk and Sanofi, as well as emerging therapies targeting similar pathways. The successful completion of this Phase 1 trial could enhance Eli Lilly's portfolio in diabetes management, particularly in combination therapies with metformin, which is a common treatment. The focus on safety and pharmacodynamics may provide a competitive edge in demonstrating the drug's efficacy and tolerability. Diligence should consider the potential for future clinical trials and regulatory pathways, as well as the evolving landscape of diabetes therapies.

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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